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PDA Training Courses

Advance Your Skills With Expert-Led, Hands-On Training in Aseptic Processing, Quality, Biotech, and More

Now through December 2025
United States . Europe . Online
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PDA Universe of Pre-Filled Syringes and Injection Devices Conference 2025

Shaping the Drug Delivery Ecosystem

21 - 22 Oct 2025
Austria Center Vienna
Vienna, Austria
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PDA Pharmaceutical Microbiology Conference 2025

Microbial Resilience: Today’s Response, Tomorrow’s Plan

27 - 29 Oct 2025
Grand Hyatt Washington
Washington, DC
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Nominations for PDA Industry and Awards

Honor a colleague, mentor, or friend for their volunteer service to PDA

Open until 01 August
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PDA Regulatory Conference 2025

Achieving CGMP Excellence: Sustainable Compliance Across the Lifecycle

08 - 10 Sep 2025
Washington, DC
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PDA BioManufacturing Conference 2025

Biomanufacturing Capabilities & Strategies – What is Next?

23 - 24 Sep 2025
DoubleTree by Hilton Rotterdam Centre
Rotterdam, The Netherlands
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Upcoming Conferences

The Americas Europe Asia-Pacific
PDA Regulatory Conference 2025
PDA Regulatory Conference 2025
07 - 12 Sep 2025
Washington, DC
PDA Capital Area Chapter Roundtable – FDA Complete Response Letters: A Growing Industry Challenge with Big Impacts
PDA Capital Area Chapter Roundtable – FDA Complete Response Letters: A Growing Industry Challenge with Big Impacts
07 Sep 2025
Washington, DC
PDA Pharmaceutical Microbiology Conference 2025
PDA Pharmaceutical Microbiology Conference 2025
26 - 31 Oct 2025
Washington, DC
PDA Week 2026
PDA Week 2026
22 - 27 Mar 2026
Denver, CO
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PDA BioManufacturing Conference 2025
PDA BioManufacturing Conference 2025
23 - 24 Sep 2025
Rotterdam, The Netherlands
PDA Universe of Pre-Filled Syringes and Injection Devices Conference 2025
PDA Universe of Pre-Filled Syringes and Injection Devices Conference 2025
21 - 22 Oct 2025
Vienna, Austria
PDA Parenteral Packaging Conference 2026
PDA Parenteral Packaging Conference 2026
14 - 15 Apr 2026
Munich, Germany
PDA Visual Inspection Forum 2026
PDA Visual Inspection Forum 2026
19 - 20 May 2026
Dublin, Ireland
PDA Miniverse: Medical Devices, Combination Products and Connected Health Conference 2026
PDA Miniverse: Medical Devices, Combination Products and Connected Health Conference 2026
21 - 22 May 2026
Dublin, Ireland
PDA Good Aseptic Manufacturing Conference 2026
PDA Good Aseptic Manufacturing Conference 2026
11 - 12 Jun 2026
Frankfurt, Germany
PDA Virus Conference 2026
PDA Virus Conference 2026
22 - 23 Jun 2026
Vienna, Austria
PDA Advanced Therapy Medicinal Products Conference 2026
PDA Advanced Therapy Medicinal Products Conference 2026
25 - 26 Jun 2026
Vienna, Austria
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PDA Aseptic Manufacturing Excellence Conference 2025
PDA Aseptic Manufacturing Excellence Conference 2025
13 - 14 Oct 2025
Melbourne, Australia
PDA Aseptic Processing of Biopharmaceuticals Conference 2025
PDA Aseptic Processing of Biopharmaceuticals Conference 2025
04 - 05 Nov 2025
Incheon, South Korea
PDA Cell and Gene Pharmaceutical Products Conference 2025
PDA Cell and Gene Pharmaceutical Products Conference 2025
18 - 19 Nov 2025
Tokyo, Japan
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Upcoming Training Courses

The Americas Europe Asia-Pacific Online
Fundamentals of Aseptic Processing Training Course (PDA 800.2)
05 - 07 Aug 2025
Denver, CO
Characteristics of Pharmaceutical Elastomers and Aluminum Seals in Parenteral Packaging Systems Training Course (PDA 808)
13 - 14 Aug 2025
Middletown, DE
Filtration Processes in the Pharmaceutical and Biopharmaceutical Industry Training Course (PDA 514)
18 - 21 Aug 2025
Bethesda, MD
Risk-Based Approach to Airflow Visualization Training Course (PDA 802.1)
26 - 28 Aug 2025
Bethesda, MD
Aseptic Processing Essentials Workshop (PDA 374)
11 Sep 2025
Washington, DC
Quality and Compliance Management for Virtual Companies Training Course (PDA 211)
11 - 12 Sep 2025
Washington, DC
Measuring Quality Culture using PDA's Assessment Tool Training Course (PDA 538.2)
11 Sep 2025
Washington, DC
Fundamentals of Quality Risk Management Training Course (PDA 529)
11 Sep 2025
Washington, DC
GxP Auditing Logistics and Inspection Readiness Training Course (Including Mock Activity) (PDA 298)
11 - 12 Sep 2025
Washington, DC
CMC Regulatory Compliance Strategy for Biopharmaceutical Manufacturing Training Course (PDA 526)
11 - 12 Sep 2025
Washington, DC
Decision-Making in Pharma Manufacturing: Ethics, Compliance, and Resilience Training Course (PDA 297)
12 Sep 2025
Washington, DC
Fundamentals of Automated Visual Inspection Training Course (PDA 593.2)
17 - 18 Sep 2025
Bethesda, MD
Mastering Aseptic Processing Training Course (PDA 100)
22 Sep - 17 Oct 2025
Bethesda, MD
Fundamentals of an Environmental Monitoring Program Training Course (PDA 102.3)
30 Sep - 02 Oct 2025
Bethesda, MD
Fundamentals of Aseptic Processing Training Course (PDA 800.2)
07 - 09 Oct 2025
Lee's Summit, MO
Single Use Systems for the Manufacturing of Parenteral Products Training Course (PDA 343)
09 - 10 Oct 2025
Bethesda, MD
Fundamentals of Cleaning and Disinfection Programs for Aseptic Manufacturing Facilities Training Course (PDA 247)
20 - 21 Oct 2025
Bethesda, MD
Validation of Moist Heat Sterilization Processes Training Course (PDA 468)
22 - 24 Oct 2025
Bethesda, MD
Developing a Microbial Monitoring Plan and Leveraging New Technologies for Effective Sterility Assurance in Aseptic Processes (PDA 542)
30 Oct 2025
Washington, DC
Environmental Monitoring Methods and Investigations – Looking for the Needle in the Haystack (PDA 618)
30 Oct 2025
Washington, DC
Mastering Aseptic Processing Training Course (PDA 100)
03 Nov - 12 Dec 2025
Bethesda, MD
Fundamentals of Aseptic Processing Training Course (PDA 800.2)
11 - 13 Nov 2025
Bethesda, MD
Performing Microbial Data Deviation Investigations in the Pharmaceutical Industry Training Course (PDA 620)
17 - 18 Nov 2025
Bethesda, MD
Design, Operation, and Qualification of Pharmaceutical Water Systems Training Course (PDA 399.1)
18 - 20 Nov 2025
Online
Foreign Particulate Examination, Isolation and Analysis Training Course (PDA 120)
19 - 20 Nov 2025
Bethesda, MD
Fundamentals of an Environmental Monitoring Program Training Course (PDA 102.3)
02 - 04 Dec 2025
Carlsbad, CA
Fundamentals of Aseptic Processing Training Course (PDA 800.2)
02 - 04 Dec 2025
Carlsbad, CA
Measuring Quality Culture using PDA's Assessment Tool Training Course (PDA 538.3)
03 - 04 Dec 2025
Online
PDA Week 2026
22 - 27 Mar 2026
Denver, CO
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PDA Manage Your Aseptic Filling Line Training Course
02 - 03 Sep 2025
Crailsheim, Germany
PDA Freeze-Drying in Practice Training Course
08 - 12 Sep 2025
Osterode am Harz, Germany
PDA All About Pre-Filled Syringe Systems - Basic Training Course Fall Edition
23 - 24 Oct 2025
Vienna, Austria
PDA Extractables and Leachables Training Course Fall Edition
23 - 24 Oct 2025
Vienna, Austria
PDA Container Closure Integrity Testing - Basic Training Course Fall Edition
23 - 24 Oct 2025
Vienna, Austria
PDA Fundamentals of Aseptic Processing Training Course
23 - 24 Oct 2025
Vienna, Austria
PDA Test Methods for Pre-Filled Syringe Systems Training Course
03 - 04 Nov 2025
Piombino Dese, Italy
PDA An Introduction to Visual Inspection: A Hands-On Training Course
12 - 13 Nov 2025
Berlin, Germany
PDA Mastering Automated Visual Inspection Training Course
12 - 13 Nov 2025
Berlin, Germany
PDA Basics of an Environmental Monitoring Program Training Course
19 - 20 Nov 2025
Berlin, Germany
View All
View All
Design, Operation, and Qualification of Pharmaceutical Water Systems Training Course (PDA 399.1)
18 - 20 Nov 2025
Online
Measuring Quality Culture using PDA's Assessment Tool Training Course (PDA 538.3)
03 - 04 Dec 2025
Online
View All

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Recent Publications

technical reports standards surveys books
Points to Consider No. 12: Restricted Access Barrier Systems
Points to Consider No. 12: Restricted Access Barrier Systems
Points to Consider No. 11: Development, Classification, Manufacture, Control, and Testing of Plasmids and Vectors Used in ATMP Production​
Points to Consider No. 11: Development, Classific...
Technical Report No. 46 (Revised 2024) Last Mile: Guidance for Good Distribution Practices for Pharmaceutical Products to End Users
Technical Report No. 46 (Revised 2024) Last Mile: ...
Technical Report No. 68 (Revised 2024): Risk-Based Approach for Prevention and Management of Drug Shortages
Technical Report No. 68 (Revised 2024): Risk-Based...
Technical Report No. 73-2: Application of Medical Device Regulation Annex 1 Requirements for Staked Needle Syringes
Technical Report No. 73-2: Application of Medical ...
Points to Consider No.9 Lessons Learned from the COVID-19 Pandemic
Points to Consider No.9 Lessons Learned from the C...
Points to Consider No.1 Aseptic Processing (Revised 2023)
Points to Consider No.1 Aseptic Processing (Revised 2023)
Technical Report No. 91 Post-Approval Change Management
Technical Report No. 91 Post-Approval Change Management
Technical Report No. 43 (Revised 2023): Identification and Classification of Nonconformities in Moulded and Tubular Glass Containers for Pharmaceutical Manufacturing
Technical Report No. 43 (Revised 2023): Identifica...
Technical Report No. 90: Contamination Control Strategy Development
Technical Report No. 90: Contamination Control Str...
Technical Report No. 89: Strategies for Vaccine Development
Technical Report No. 89: Strategies for Vaccine Development
Points to Consider for Microbial Control in ATMP Manufacturing (Single user digital version)
Points to Consider for Microbial Control in ATMP M...
Technical Report No.41 Revised 2022 (TR 41): Virus Filtration
Technical Report No.41 Revised 2022 (TR 41): Virus Filtration
PDA Technical Report No.65 Revised 2022 (TR 65) Technology Transfer (Single user digital version)
PDA Technical Report No.65 Revised 2022 (TR 65) Te...
Points to Consider in Remote and Hybrid GMP/GDP Audits (single user digital version)
Points to Consider in Remote and Hybrid GMP/GDP Au...
PDA Technical Report No. 13 Revised 2022 (TR 13) Fundamentals of an Environmental Monitoring Program (single user digital version)
PDA Technical Report No. 13 Revised 2022 (TR 13) F...
PDA Technical Report No. 88 (TR 88) Microbial Data Deviation Investigations in the Pharmaceutical Industry
PDA Technical Report No. 88 (TR 88) Microbial Data...
PDA Technical Report No. 39 Revised 2021 (TR 39) Guidance for Temperature-Controlled Medicinal Products - Maintaining the Quality of Temperature-Sensitive Medicinal Products through the Transportation Environment (single user digital version)
PDA Technical Report No. 39 Revised 2021 (TR 39) G...
PDA Technical Report No. 87 (TR 87) Current Best Practices for Pharmaceutical Glass Vial Handling and Processing (single user digital version)
PDA Technical Report No. 87 (TR 87) Current Best P...
Points to Consider in Remote and Hybrid GMP/GDP Inspections
Points to Consider in Remote and Hybrid GMP/GDP Inspections
PDA Technical Report No. 86 (TR 86) Industry Challenges and Current Technologies for Pharmaceutical Package Integrity Testing (single user digital version)
PDA Technical Report No. 86 (TR 86) Industry Chall...
PDA Technical Report No. 85 (TR 85) Enhanced Test Methods for Visible Particle Detection and Enumeration on Elastomeric Closures and Glass Containers (single user digital version)
PDA Technical Report No. 85 (TR 85) Enhanced Test ...
PDA Technical Report No. 60-3 (TR 60-3) Process Validation: A Lifecycle Approach, Annex 2: Biopharmaceutical Drug Substances Manufacturing (single user digital version)
PDA Technical Report No. 60-3 (TR 60-3) Process Va...
Reporte Tecnico No. 1 (Revisado en 2007) Validacion de los Procesos de Esterilizacion por Calor Humedo: Diseno del Ciclo, Desarrollo, Calificacion y Control Continuo (versión digital de un solo usuario)
Reporte Tecnico No. 1 (Revisado en 2007) Validacio...
PDA Technical Report No. 13-2 (TR 13-2) Fundamentals of an Environmental Monitoring Program Annex 1: Environmental Monitoring of Facilities Manufacturing Low Bioburden Products (single user digital version)
PDA Technical Report No. 13-2 (TR 13-2) Fundamenta...
PDA Technical Report No. 84 (TR 84) Integrating Data Integrity Requirements into Manufacturing & Packaging Operations (single user digital version)
PDA Technical Report No. 84 (TR 84) Integrating Da...
Points to Consider for Implementation of Pre-Use Post-Sterilization Integrity Testing (PUPSIT)
Points to Consider for Implementation of Pre-Use P...
Points to Consider for Risks Associated with Sterilizing Grade Filters and Sterilizing Filtration
Points to Consider for Risks Associated with Steri...
Points to Consider for Sensitivity to Oxidation by Peroxide
Points to Consider for Sensitivity to Oxidation by Peroxide
Points to Consider for the Aseptic Processing of Sterile Pharmaceutical Products in Isolators
Points to Consider for the Aseptic Processing of S...
PDA Technical Report No. 54-6 (TR 54-6) Formalized Risk Assessment for Excipients (single user digital version)
PDA Technical Report No. 54-6 (TR 54-6) Formalized...
PDA Technical Report No. 83 (TR 83) Virus Contamination in Biomanufacturing: Risk Mitigation, Preparedness, and Response (single user digital version)
PDA Technical Report No. 83 (TR 83) Virus Contamin...
PDA Reporte Tecnico No. 13 (Revisado) Fundamentos de un Programa de Monitoreo Ambiental en Español (versión digital de un solo usuario)
PDA Reporte Tecnico No. 13 (Revisado) Fundamentos ...
PDA Technical Report No. 82 (TR 82) Low Endotoxin Recovery (single user digital version)
PDA Technical Report No. 82 (TR 82) Low Endotoxin ...
PDA Technical Report No. 81 (TR 81) Cell-Based Therapy Control Strategy (single user digital version)
PDA Technical Report No. 81 (TR 81) Cell-Based The...
PDA Technical Report No. 80 (TR 80) Data Integrity Management System for Pharmaceutical Laboratories (single user digital version)
PDA Technical Report No. 80 (TR 80) Data Integrity...
PDA Technical Report No. 79 (TR 79) Particulate Matter Control in Difficult to Inspect Parenterals (single user digital version)
PDA Technical Report No. 79 (TR 79) Particulate Ma...
PDA Technical Report No. 78 (TR 78) Particulate Matter in Oral Dosage Forms (single user digital version)
PDA Technical Report No. 78 (TR 78) Particulate Ma...
Points to Consider for Aging Facilities
Points to Consider for Aging Facilities
PDA Technical Report No. 54-5 (TR 54-5) Quality Risk Management for the Design, Qualification, and Operation of Manufacturing Systems (single user digital version)
PDA Technical Report No. 54-5 (TR 54-5) Quality Ri...
PDA Technical Report No. 60-2 (TR 60-2) Process Validation: A Lifecycle Approach, Annex 1: Oral Solid Dosage/Semisolid Dosage Forms (single user digital version)
PDA Technical Report No. 60-2 (TR 60-2) Process Va...
PDA Technical Report No. 77 (TR 77) The Manufacture of Sterile Pharmaceutical Products Using Blow-Fill-Seal Technology (single user digital version)
PDA Technical Report No. 77 (TR 77) The Manufactur...
PDA Technical Report No. 56 Revised 2016 (TR 56) Application of Phase-Appropriate Quality System and cGMP to the Development of Therapeutic Protein Drug Substance (API or Biological Active Substance) (single user digital version)
PDA Technical Report No. 56 Revised 2016 (TR 56) A...
PDA Technical Report No. 76 (TR 76) Identification and Classification of Visible Nonconformities in Elastomeric Components and Aluminum Seals for Parenteral Packaging (single user digital version)
PDA Technical Report No. 76 (TR 76) Identification...
PDA Technical Report No. 75 (TR 75) Consensus Method for Rating 0.1μm Mycoplasma Reduction Filters (single user digital version)
PDA Technical Report No. 75 (TR 75) Consensus Meth...
PDA Technical Report No. 74 (TR 74) Reprocessing of Biopharmaceuticals (single user digital version)
PDA Technical Report No. 74 (TR 74) Reprocessing o...
PDA Technical Report No. 73 (TR 73) Prefilled Syringe User Requirements for Biotechnology Applications (single user digital version)
PDA Technical Report No. 73 (TR 73) Prefilled Syri...
PDA Technical Report No. 72 (TR 72) Passive Thermal Protection Systems for Global Distribution: Qualification and Operational Guidance (single user digital version)
PDA Technical Report No. 72 (TR 72) Passive Therma...
PDA Technical Report No. 71 (TR 71) Emerging Methods for Virus Detection (single user digital version)
PDA Technical Report No. 71 (TR 71) Emerging Metho...
PDA Technical Report No. 70 (TR 70) Fundamentals of Cleaning and Disinfection Programs for Aseptic Manufacturing Facilities (single user digital version)
PDA Technical Report No. 70 (TR 70) Fundamentals o...
PDA Technical Report No. 69 (TR 69) Bioburden and Biofilm Management in Pharmaceutical Manufacturing Operations (single user digital version)
PDA Technical Report No. 69 (TR 69) Bioburden and ...
PDA Technical Report No. 57-2, (TR 57-2) Analytical Method Development and Qualification for Biotechnology Products (single user digital version)
PDA Technical Report No. 57-2, (TR 57-2) Analytica...
PDA Technical Report No. 54-4, (TR 54-4) Implementation of Quality Risk Management for Pharmaceutical and Biotechnology Manufacturing Operations: Annex 3: Case Studies in the Mfg of Biotechnological Bulk Drug Substances (single user digital version)
PDA Technical Report No. 54-4, (TR 54-4) Implement...
PDA Technical Report No. 67, (TR 67) Exclusion of Objectionable Microorganisms from Nonsterile Pharmaceuticals, Medical Devices, and Cosmetics (single user digital version)
PDA Technical Report No. 67, (TR 67) Exclusion of ...
PDA Technical Report No. 66, (TR 66) Application of Single-Use Systems in Pharmaceutical Manufacturing (single user digital version)
PDA Technical Report No. 66, (TR 66) Application o...
PDA Technical Series: Sterilization — Compilation of Technical Reports and Journal Articles on Pharmaceutical Sterilization (single user digital version)
PDA Technical Series: Sterilization — Compilation ...
PDA Technical Report No. 54-3 (TR 54-3) Implementation of Quality Risk Management for Pharmaceutical and Biotechnology Manufacturing Operations:Annex 2: Case Studies in the Manufacturing of Pharmaceutical Drug Products (single user digital version)
PDA Technical Report No. 54-3 (TR 54-3) Implementa...
PDA Technical Report No. 33, Revised 2013 (TR 33) Evaluation, Validation and Implementation of Alternative and Rapid Microbiological Methods (single user digital version)
PDA Technical Report No. 33, Revised 2013 (TR 33) ...
PDA Technical Report No. 64 (TR 64) Active Temperature-Controlled Systems: Qualification Guidance (single user digital version)
PDA Technical Report No. 64 (TR 64) Active Tempera...
PDA Technical Report No. 63 (TR 63) Quality Requirements for the Extemporaneous Preparation of Clinical Trial Materials (single user digital version)
PDA Technical Report No. 63 (TR 63) Quality Requir...
PDA Technical Report No. 3, Revised 2013 (TR 3) Validation of Dry Heat Processes Used for Depyrogenation and Sterilization (single user digital version)
PDA Technical Report No. 3, Revised 2013 (TR 3) V...
PDA Technical Report No. 62 (TR 62) Recommended Practices for Manual Aseptic Processes (single user digital version)
PDA Technical Report No. 62 (TR 62) Recommended Pr...
PDA Technical Report No. 54-2(TR 54-2) Implementation of Quality Risk Management for Pharmaceutical & Biotechnology Manufacturing Operation:Annex 1: Case Study Examples for Quality Risk Management in Packaging & Labeling (single user digital version)
PDA Technical Report No. 54-2(TR 54-2) Implementat...
PDA Technical Report No. 61 (TR 61) Steam In Place
PDA Technical Report No. 61 (TR 61) Steam In Place
PDA Technical Report No. 60 (TR 60) Process Validation: A Lifecycle Approach (single user digital version)
PDA Technical Report No. 60 (TR 60) Process Valida...
PDA Technical Report No. 29, Revised 2012 (TR 29) Points to Consider for Cleaning Validation (single user digital version)
PDA Technical Report No. 29, Revised 2012 (TR 29) ...
PDA Technical Report No. 59 (TR 59) Utilization of Statistical Methods for Production Monitoring (single user digital version)
PDA Technical Report No. 59 (TR 59) Utilization of...
PDA Technical Report No. 58 (TR 58) Risk Management for Temperature-Controlled Distribution (single user digital version)
PDA Technical Report No. 58 (TR 58) Risk Managemen...
PDA Technical Report Distribution Series
PDA Technical Report Distribution Series
PDA Technical Report No. 57 (TR 57) Analytical Method Validation and Transfer for Biotechnology Products (single user digital version)
PDA Technical Report No. 57 (TR 57) Analytical Met...
PDA Technical Report No. 55 (TR 55) Detection and Mitigation of 2,4,6-Tribromoanisole and 2,4,6-Trichloroanisole Taints and Odors in the Pharmaceutical and Consumer Healthcare Industries (single user digital version)
PDA Technical Report No. 55 (TR 55) Detection and ...
PDA Technical Report No. 54 (TR 54) Implementation of Quality Risk Management for Pharmaceutical and Biotechnology Manufacturing Operations (single user digital version)
PDA Technical Report No. 54 (TR 54) Implementation...
Technical Report No. 44, (TR 44): Quality Risk Management for Aseptic Processes
Technical Report No. 44, (TR 44): Quality Risk Man...
PDA Technical Report No. 1, Revised 2007, (TR 1) Validation of Moist Heat Sterilization Processes Cycle Design, Development, Qualification and Ongoing Control
PDA Technical Report No. 1, Revised 2007, (TR 1) ...
Technical Report No. 45 (TR 45): Filtration of Liquids Using Cellulose-Based Depth Filters
Technical Report No. 45 (TR 45): Filtration of Liq...
Technical Report No. 49 (TR 49): Points to Consider for Biotechnology Cleaning Validation
Technical Report No. 49 (TR 49): Points to Conside...
Technical Report No. 48 (TR 48): Moist Heat Sterilizer Systems: Design, Commissioning, Operation, Qualification and Maintenance
Technical Report No. 48 (TR 48): Moist Heat Steril...
PDA Technical Report No. 51 (TR 51) Biological Indicators for Gas and Vapor-Phase Decontamination Processes: Specification, Manufacture, Control and Use (single user digital version)
PDA Technical Report No. 51 (TR 51) Biological Ind...
PDA Technical Report No. 50 (TR 50) Alternative Methods for Mycoplasma Testing (single user digital version)
PDA Technical Report No. 50 (TR 50) Alternative Me...
Technical Report No. 47 (TR 47): Preparation of Virus Spikes Used for Virus Clearance Studies
Technical Report No. 47 (TR 47): Preparation of Vi...
PDA Technical Report No. 53 (TR 53) Guidance for Industry: Stability Testing to Support Distribution of New Drug Products (single user digital version)
PDA Technical Report No. 53 (TR 53) Guidance for I...
PDA Technical Report No. 52 (TR 52) Guidance for Good Distribution Practices (GDPs) For the Pharmaceutical Supply Chain (single user digital version)
PDA Technical Report No. 52 (TR 52) Guidance for G...
PDA Technical Report No. 20, (TR 20) Report on Survey of Current Industry Gowning Practices (single user digital version)
PDA Technical Report No. 20, (TR 20) Report on Sur...
PDA Technical Report No. 36, (TR 36) Current Practices in the Validation of Aseptic Processing - 2001 (single user digital version)
PDA Technical Report No. 36, (TR 36) Current Pract...
PDA Technical Report No. 35, (TR 35) A Proposed Training Model for the Microbiological Function in the Pharmaceutical Industry (single user digital version)
PDA Technical Report No. 35, (TR 35) A Proposed Tr...
PDA Technical Report No. 34, (TR 34) Design and Validation of Isolator Systems for the Manufacturing and Testing of Health Care Products (single user digital version)
PDA Technical Report No. 34, (TR 34) Design and Va...
PDA Technical Report No. 31, (TR 31) Validation and Qualification of Computerized Laboratory Data Acquisition Systems (single user digital version)
PDA Technical Report No. 31, (TR 31) Validation an...
PDA Technical Report No. 30 Revised 2012, (TR 30) Parametric Release of Pharmaceuticals and Medical Device Products Terminally Sterilized by Moist Heat (single user digital version)
PDA Technical Report No. 30 Revised 2012, (TR 30) ...
PDA Technical Report No. 28 Revised, (TR 28) Process Simulation Testing for Sterile Bulk Pharmaceutical Chemicals (single user digital version)
PDA Technical Report No. 28 Revised, (TR 28) Proce...
PDA Technical Report No. 27, (TR 27) Pharmaceutical Package Integrity (single user digital version)
PDA Technical Report No. 27, (TR 27) Pharmaceutica...
PDA Technical Report No. 26, (TR 26) Revised 2008, Sterilizing Filtration of Liquids (single user digital version)
PDA Technical Report No. 26, (TR 26) Revised 2008,...
PDA Technical Report No. 25, (TR 25) Blend Uniformity Analysis: Validation and In-Process Testing (single user digital version)
PDA Technical Report No. 25, (TR 25) Blend Uniform...
PDA Technical Report No. 24, (TR 24) Current Practices in the Validation of Aseptic Processing - 1996 (single user digital version)
PDA Technical Report No. 24, (TR 24) Current Pract...
PDA Technical Report No. 23, (TR 23) Industry Survey on Current Sterile Filtration Practices
PDA Technical Report No. 23, (TR 23) Industry Surv...
PDA Technical Report No. 22, (TR 22) Revised 2011 Process Simulation for Aseptically Filled Products
PDA Technical Report No. 22, (TR 22) Revised 2011 ...
PDA Technical Report No. 19, (TR 19) Rapid/Automated ID Methods Survey
PDA Technical Report No. 19, (TR 19) Rapid/Automat...
PDA Technical Report No. 18, (TR 18) Validation of Computer-Related Systems
PDA Technical Report No. 18, (TR 18) Validation of...
PDA Technical Report No. 17, (TR 17) Current Practices in the Validation of Aseptic Processing - 1992
PDA Technical Report No. 17, (TR 17) Current Pract...
PDA Technical Report No. 16, (TR 16) Effect of Gamma Irradiation on Elastomeric Closures
PDA Technical Report No. 16, (TR 16) Effect of Gam...
PDA Technical Report No. 15, Revised 2009 (TR 15) Validation of Tangential Flow Filtration in Biopharmaceutical Applications
PDA Technical Report No. 15, Revised 2009 (TR 15) ...
PDA Technical Report No. 14, (TR 14) Validation of Column-Based Chromatography Processes for the Purification of Proteins
PDA Technical Report No. 14, (TR 14) Validation of...
PDA Technical Report No. 12, (TR 12) Siliconization of Parenteral Drug Packaging Components
PDA Technical Report No. 12, (TR 12) Siliconizatio...
PDA Technical Report No. 11, (TR 11) Sterilization of Parenterals by Gamma Radiation
PDA Technical Report No. 11, (TR 11) Sterilization...
PDA Technical Report No. 10, (TR 10) Parenteral Formulations of Proteins and Peptides: Stability and Stabilizers
PDA Technical Report No. 10, (TR 10) Parenteral Fo...
PDA Technical Report No. 9, (TR 9) Review of Commercially Available Particulate Measurement Systems
PDA Technical Report No. 9, (TR 9) Review of Comme...
PDA Technical Report No. 7, (TR 7) Depyrogenation (single user digital version)
PDA Technical Report No. 7, (TR 7) Depyrogenation ...
PDA Technical Report No. 5, (TR 5) Sterile Pharmaceutical Packaging: Compatibility and Stability (single user digital version)
PDA Technical Report No. 5, (TR 5) Sterile Pharma...
Technical Report No. 4, (TR 4): Design Concepts for the Validation of Water for Injection System
Technical Report No. 4, (TR 4): Design Concepts f...
Technical Report No. 38: Manufacturing Chromatography Systems Postapproval Changes (ChromPAC): Chemistry, Manufacturing and Controls Documentation
Technical Report No. 38: Manufacturing Chromatogr...
Technical Report No. 40: Sterilizing Filtration of Gases
Technical Report No. 40: Sterilizing Filtration of Gases
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PDA/ANSI Standard 06-2025: Assessment of Quality Culture Guidance Documents, Models, and Tools
PDA/ANSI Standard 06-2025: Assessment of Quality C...
PDA/ANSI Standard 03-2025: Standard Practice for Quality Risk Management of Aseptic Processes
PDA/ANSI Standard 03-2025: Standard Practice for Q...
ANSI/PDA Standard 02-2021: Cryopreservation of Cells for Use in Cell Therapies, Gene Therapies, and Regenerative Medicine Manufacturing
ANSI/PDA Standard 02-2021: Cryopreservation of Cel...
ANSI/PDA Standard 05-2021: Consensus Method for Rating Filters for Mycoplasma Reduction
ANSI/PDA Standard 05-2021: Consensus Method for Ra...
ANSI/PDA Standard 04-2021: Phage Retention Nomenclature Rating for Small- and Large-Virus Retentive Filters
ANSI/PDA Standard 04-2021: Phage Retention Nomencl...
ANSI/PDA Standard 001-2020: Enhanced Purchasing Controls to Support the Bio-Pharmaceutical, Pharmaceutical, Medical Devices and Combination Products Industries
ANSI/PDA Standard 001-2020: Enhanced Purchasing Co...
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PDA Survey: 2025 Transportation Validation Benchmarking Survey
PDA Survey: 2025 Transportation Validation Benchmarking Survey
PDA Survey: 2024 PDA Annex 1: One Year into Implementation Survey
PDA Survey: 2024 PDA Annex 1: One Year into Implementation Survey
PDA Survey: Implementation of the New EU GMP Annex 1 and Implementation of Barrier Systems Survey
PDA Survey: Implementation of the New EU GMP Annex...
PDA Survey: Availability of Single-Use-System Components and its Potential Impact on Product Supply Survey Results
PDA Survey: Availability of Single-Use-System Comp...
PDA Research: 2023 PDA Visual Inspection Survey (single user digital version)
PDA Research: 2023 PDA Visual Inspection Survey (s...
PDA Research: 2021 PDA Aseptic Processing Simulation Survey (Single user digital version)
PDA Research: 2021 PDA Aseptic Processing Simulati...
PDA Research: 2020 Particulate Matter in Flexible Containers Survey (single user digital version)
PDA Research: 2020 Particulate Matter in Flexible ...
PDA Research: 2021 Post-Approval Change Issues and Impacts Survey (single user digital version)
PDA Research: 2021 Post-Approval Change Issues and...
PDA Research: 2019 PDA Traceability of Primary Packaging Survey (single user digital version)
PDA Research: 2019 PDA Traceability of Primary Pac...
PDA Research: 2019 Sterile Lyophilized Drug Product Loading Survey (single user digital version)
PDA Research: 2019 Sterile Lyophilized Drug Produc...
PDA Research: 2019 Technology Transfer Industry Survey (single user digital version)
PDA Research: 2019 Technology Transfer Industry Su...
PDA Research: 2017 PDA Glass Quality Survey (single user digital version)
PDA Research: 2017 PDA Glass Quality Survey (singl...
PDA Research: 2017 PDA PUPSIT Survey (single user digital version)
PDA Research: 2017 PDA PUPSIT Survey (single user ...
PDA Research: 2017 PDA Aseptic Processing Survey (single user digital version)
PDA Research: 2017 PDA Aseptic Processing Survey (...
Quality Culture Metrics Pilot Report (single user digital version)
Quality Culture Metrics Pilot Report (single user ...
PDA Survey: 2015 Aging Facilities (single user digital version)
PDA Survey: 2015 Aging Facilities (single user digital version)
PDA Survey: 2015 Particulate Matter in Difficult to Inspect Parenterals (single user digital version)
PDA Survey: 2015 Particulate Matter in Difficult t...
PDA Survey: 2015 Particulate Matter in Oral Dosage Forms (single user digital version)
PDA Survey: 2015 Particulate Matter in Oral Dosage...
PDA Survey: 2014 Visual Inspection (single user digital version)
PDA Survey: 2014 Visual Inspection (single user digital version)
PDA Survey: 2014 Quality Culture Metrics (single user digital version)
PDA Survey: 2014 Quality Culture Metrics (single u...
PDA Survey: 2014 PDA Process Validation Survey (single user digital version)
PDA Survey: 2014 PDA Process Validation Survey (si...
PDA Survey: 2013 PDA Objectionable Microorganisms for Nonsterile Pharmaceutical, Consumer Health, Medical Devices, Dietary Supplement and Cosmetic Products (single user digital version)
PDA Survey: 2013 PDA Objectionable Microorganisms ...
PDA Survey: Glass Quality: 2011 and 2012 Results and Comparison (single user digital version)
PDA Survey: Glass Quality: 2011 and 2012 Results a...
PDA Survey: Business Case for Pharmaceutical Quality (single user digital version)
PDA Survey: Business Case for Pharmaceutical Quali...
Risk Mitigation of Tribromoanisole (TBA)/Trichloroanisole (TCA) Taints and Odors: A Pharmaceutical Industry Benchmarking Survey (single user digital version)
Risk Mitigation of Tribromoanisole (TBA)/Trichloro...
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Environmental Monitoring Volume 9
Environmental Monitoring Volume 9
Quality Risk Management: A Practical Guide
Quality Risk Management: A Practical Guide
Global Sterile Manufacturing Regulatory Guidance Comparison & Assessment Tool Second Edition
Global Sterile Manufacturing Regulatory Guidance C...
GMP Validation: A Guide to International Regulatory Requirements
GMP Validation: A Guide to International Regulatory Requirements
Industrial Pharmaceutical Microbiology Quality Control
Industrial Pharmaceutical Microbiology Quality Control
Industrial Pharmaceutical Microbiology Standards & Controls 6th Edition
Industrial Pharmaceutical Microbiology Standards &...
Conducting Compliant Investigations
Conducting Compliant Investigations
Quality by Design - An Indispensable Approach to Accelerate Biopharmaceutical Product Development (single user digital version)
Quality by Design - An Indispensable Approach to A...
Cleanroom Contamination Prevention & Control: A Practical Guide to the Science (single user digital version)
Cleanroom Contamination Prevention & Control: A Pr...
Digital Transformation and Regulatory Considerations for Biopharmaceutical and Healthcare Manufacturers, Volume 2: Digital Data, Insights, Metrics and Analytics (single user digital version)
Digital Transformation and Regulatory Consideratio...
Digital Transformation and Regulatory Considerations for Biopharmaceutical and Healthcare Manufacturers, Volume 1: Digital Technologies for Automation and Process Improvement (single user digital version)
Digital Transformation and Regulatory Consideratio...
Water Activity Applications in the Pharmaceutical Industry (single user digital version)
Water Activity Applications in the Pharmaceutical ...
Root Cause Investigations for CAPA: Clear and Simple (single user digital version)
Root Cause Investigations for CAPA: Clear and Simp...
Software as a Service (SaaS): Risk-Based Validation with Time-Saving Templates (single user digital version)
Software as a Service (SaaS): Risk-Based Validatio...
FDA Warning Letters: Analysis and Guidance (single user digital version)
FDA Warning Letters: Analysis and Guidance (single...
Fungi: A Handbook for Life Science Manufacturers and Researchers (single user digital version)
Fungi: A Handbook for Life Science Manufacturers a...
Risk-Based Software Validation (Single user digital version)
Risk-Based Software Validation (Single user digital version)
Good Distribution Practice: A Handbook for Healthcare Manufacturers and Suppliers, Volume 2 (single user digital version)
Good Distribution Practice: A Handbook for Healthc...
Biotechnology: From Idea to Market (single user digital version)
Biotechnology: From Idea to Market (single user digital version)
Audit and Control for Healthcare Manufacturers: A Systems-Based Approach (single user digital version)
Audit and Control for Healthcare Manufacturers: A ...
PDA Technical Series: Endotoxin Analysis and Risk Management
PDA Technical Series: Endotoxin Analysis and Risk Management
Microbiology in Pharmaceutical Manufacturing, Second Edition, Revised and Expanded, Volume 2 (single user digital version)
Microbiology in Pharmaceutical Manufacturing, Seco...
Microbiology in Pharmaceutical Manufacturing, Second Edition, Revised and Expanded, Volume 1 (single user digital version)
Microbiology in Pharmaceutical Manufacturing, Seco...
PDA Technical Series: Pharmaceutical Glass
PDA Technical Series: Pharmaceutical Glass
Phase Appropriate GMP for Biological Processes: Pre-clinical to Commercial Production (single user digital version)
Phase Appropriate GMP for Biological Processes: Pr...
Contamination Prevention for Nonsterile Pharmaceutical Manufacturing
Contamination Prevention for Nonsterile Pharmaceut...
Microbiological Culture Media: A Complete Guide for Pharmaceutical and Healthcare Manufacturers (single user digital version)
Microbiological Culture Media: A Complete Guide fo...
Torbeck`s Statistical Cookbook for Scientists and Engineers (single user digital version)
Torbeck`s Statistical Cookbook for Scientists and ...
Environmental Monitoring: A Comprehensive Handbook, Volume 8 (single user digital version)
Environmental Monitoring: A Comprehensive Handbook...
Aseptic and Sterile Processing: Control, Compliance and Future Trends (single user digital version)
Aseptic and Sterile Processing: Control, Complianc...
Cleaning Validation: Practical Compliance Solutions for Pharmaceutical Manufacturing, Volume 3 (single user digital version)
Cleaning Validation: Practical Compliance Solution...
Cleaning Validation: Practical Compliance Solutions for Pharmaceutical Manufacturing, Volume 2 (single user digital version)
Cleaning Validation: Practical Compliance Solution...
Cleaning Validation: Practical Compliance Solutions for Pharmaceutical Manufacturing, Volume 1 (single user digital version)
Cleaning Validation: Practical Compliance Solution...
Cleaning Validation: Practical Compliance Solutions for Pharmaceutical Manufacturing, Volume 4 (single user digital version)
Cleaning Validation: Practical Compliance Solution...
Effective Implementation of Audit Programs (single user digital version)
Effective Implementation of Audit Programs (single...
Method Development and Validation for the Pharmaceutical Microbiologist (single user digital version)
Method Development and Validation for the Pharmace...
Pharmaceutical Quality Control Microbiology: A Guidebook to the Basics (single user digital version)
Pharmaceutical Quality Control Microbiology: A Gui...
Essential Microbiology for QP Candidates (single user digital version)
Essential Microbiology for QP Candidates (single u...
Biological Indicators for Sterilization Processes (single user digital version)
Biological Indicators for Sterilization Processes ...
Recent Warning Letters Review for Preparation of a Non-Sterile Processing Inspection, Volume 2 (single user digital version)
Recent Warning Letters Review for Preparation of a...
Lifecycle Risk Management for Healthcare Products: From Research Through Disposal (single user digital version)
Lifecycle Risk Management for Healthcare Products:...
Recent Warning Letters Review for Preparation of an Aseptic Processing Inspection, Volume 1 (single user digital version)
Recent Warning Letters Review for Preparation of a...
Risk Assessment and Management for Healthcare Manufacturing: Practical Tips and Case Studies (single user digital version)
Risk Assessment and Management for Healthcare Manu...
Contamination Control in Healthcare Product Manufacturing, Volume 4 (single user digital version)
Contamination Control in Healthcare Product Manufa...
Pharmaceutical Legislation of the European Union, Japan and the United States of America - An Overview, Updated and Expanded Second Edition
Pharmaceutical Legislation of the European Union, ...
Assuring Data Integrity for Life Sciences (single user digital version)
Assuring Data Integrity for Life Sciences (single ...
Visual Inspection and Particulate Control (single user digital version)
Visual Inspection and Particulate Control (single ...
Why Life Science Manufacturers Do What They Do in Development, Formulation, Production and Quality: A History (single user digital version)
Why Life Science Manufacturers Do What They Do in ...
Lessons of Failure: When Things Go Wrong In Pharmaceutical Manufacturing (single user digital version)
Lessons of Failure: When Things Go Wrong In Pharma...
Trend and Out-of-Trend Analysis for Pharmaceutical Quality and Manufacturing Using Minitab (single user digital version)
Trend and Out-of-Trend Analysis for Pharmaceutical...
Environmental Monitoring: A Comprehensive Handbook, Volumes 4, 5, 6 and 7
Environmental Monitoring: A Comprehensive Handbook...
Environmental Monitoring: A Comprehensive Handbook, Volume 1, 2 and 3 (single user digital version)
Environmental Monitoring: A Comprehensive Handbook...
Environmental Monitoring: A Comprehensive Handbook, Volume 4 (single user digital version)
Environmental Monitoring: A Comprehensive Handbook...
Environmental Monitoring: A Comprehensive Handbook, Volume 5 (single user digital version)
Environmental Monitoring: A Comprehensive Handbook...
Environmental Monitoring: A Comprehensive Handbook, Volume 6 (single user digital version)
Environmental Monitoring: A Comprehensive Handbook...
Environmental Monitoring: A Comprehensive Handbook, Volume 7 (single user digital version)
Environmental Monitoring: A Comprehensive Handbook...
Microbial Risk and Investigations (single user digital version)
Microbial Risk and Investigations (single user digital version)
Computerized Systems in the Modern Laboratory: A Practical Guide (single user digital version)
Computerized Systems in the Modern Laboratory: A P...
Encyclopedia of Rapid Microbiol Methods, Volume 4
Encyclopedia of Rapid Microbiol Methods, Volume 4
Encyclopedia of Rapid Microbiological Methods, Volumes 1, 2 and 3 (single user digital version)
Encyclopedia of Rapid Microbiological Methods, Vol...
Cleaning and Cleaning Validation, Volumes 1 and 2 (single user digital version)
Cleaning and Cleaning Validation, Volumes 1 and 2 ...
Rapid Sterility Testing (single user digital version)
Rapid Sterility Testing (single user digital version)
Microbiology in Pharmaceutical Manufacturing, Second Edition, Revised and Expanded, Volumes 1 and 2 (single user digital version)
Microbiology in Pharmaceutical Manufacturing, Seco...
Practical Aseptic Processing Fill and Finish, Volumes 1 and 2 (single user digital version)
Practical Aseptic Processing Fill and Finish, Volu...
Thermal Validation in Moist Heat Sterilization (single user digital version)
Thermal Validation in Moist Heat Sterilization (si...
Validating Enterprise Systems: A Practical Guide (single user digital version)
Validating Enterprise Systems: A Practical Guide (...
Laboratory Design: Establishing the Facility and Management Structure (single user digital version)
Laboratory Design: Establishing the Facility and M...
Validation by Design: The Statistical Handbook for Pharmaceutical Process Validation (single user digital version)
Validation by Design: The Statistical Handbook for...
Biofilm Control in Drug Manufacturing (single user digital version)
Biofilm Control in Drug Manufacturing (single user...
Sterility Testing of Pharmaceutical Products (single user digital version)
Sterility Testing of Pharmaceutical Products (sing...
Risk Assessment and Risk Management in the Pharmaceutical Industry: Clear and Simple (single user digital version)
Risk Assessment and Risk Management in the Pharmac...
The Bacterial Endotoxins Test: A Practical Guide (single user digital version)
The Bacterial Endotoxins Test: A Practical Guide (...
Quality By Design: Putting Theory Into Practice (single user digital version)
Quality By Design: Putting Theory Into Practice (s...
Pharmaceutical Outsourcing: Quality Management and Project Delivery (single user digital version)
Pharmaceutical Outsourcing: Quality Management and...
Technology and Knowledge Transfer: Keys to Successful Implementation and Management (single user digital version)
Technology and Knowledge Transfer: Keys to Success...
Cleanroom Microbiology (single user digital version)
Cleanroom Microbiology (single user digital version)
Square Root of (N) Sampling Plans: Procedures and Tables for Inspection of Quality Attributes (single user digital version)
Square Root of (N) Sampling Plans: Procedures and ...
Cleaning Validation: Practical Compliance Solutions for Pharmaceutical Manufacturing, Volumes 1, 2 & 3 (single user digital version)
Cleaning Validation: Practical Compliance Solution...
Cold Chain Chronicles: A practitioners outside-the-box perspectives on the importance of temperature-sensitive drug stewardship (single user digital version)
Cold Chain Chronicles: A practitioners outside-the...
Environmental Monitoring: A Comprehensive Handbook, Volume 3 (single user digital version)
Environmental Monitoring: A Comprehensive Handbook...
Environmental Monitoring: A Comprehensive Handbook, Volume 2 (single user digital version)
Environmental Monitoring: A Comprehensive Handbook...
Environmental Monitoring: A Comprehensive Handbook, Volume 1 (single user digital version)
Environmental Monitoring: A Comprehensive Handbook...
Contamination Control in Healthcare Product Manufacturing, Volumes 1, 2 & 3 (single user digital version)
Contamination Control in Healthcare Product Manufa...
Contamination Control in Healthcare Product Manufacturing, Volume 2 (single user digital version)
Contamination Control in Healthcare Product Manufa...
Contamination Control in Healthcare Product Manufacturing, Volume 3 (single user digital version)
Contamination Control in Healthcare Product Manufa...
Risk-Based Compliance Handbook (single user digital version)
Risk-Based Compliance Handbook (single user digital version)
Systems Based Inspection for Pharmaceutical Manufacturers (single user digital version)
Systems Based Inspection for Pharmaceutical Manufa...
Validation of Analytical Methods for Biopharmaceuticals: A Guide to Risk-Based Validation and Implementation Strategies (single user digital version)
Validation of Analytical Methods for Biopharmaceut...
Microbial Identification: The Keys to a Successful Program (single user digital version)
Microbial Identification: The Keys to a Successful...
Contamination Control in Healthcare Product Manufacturing, Volume 1 (single user digital version)
Contamination Control in Healthcare Product Manufa...
Combination Products: Implementation of cGMP Requirements
Combination Products: Implementation of cGMP Requirements
Environmental Monitoring: A Comprehensive Handbook, Volume 4 (Hardcover)
Environmental Monitoring: A Comprehensive Handbook...
Ethylene Oxide Sterilization Validation and Routine Operations Handbook (single user digital version)
Ethylene Oxide Sterilization Validation and Routin...
Microbial Risk Assessment in Pharmaceutical Clean Rooms (single user digital version)
Microbial Risk Assessment in Pharmaceutical Clean ...
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