PDA Quality and Compliance Training Courses
PDA's Quality and Compliance training courses map how the following pieces will assist with the manufacturing production and distribution of safe and compliant parenteral products: audit, quality management systems design, GDP/cGMP compliance, training, SOP development, the role of qualified/responsible people, inspection, and quality risk management.
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Starting 11 Sep
Quality and Compliance Management for Virtual Companies Training Course (PDA 211)
- Sep 11 - Sep 12, 2025
- Washington
- , DC
This training course provides attendees with a foundational understanding of the GMP, GCP and GLP requirements for virtual companies and how to evaluate their company's quality system structure. -
11 Sep
Measuring Quality Culture using PDA's Assessment Tool Training Course (PDA 538.2)
- Sep 11, 2025
- Washington
- , DC
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11 Sep
Pharmaceutical Manufacturing Code of Ethics Training Course (PDA 297)
- Sep 11, 2025
- Washington
- , DC
This training course is designed to strengthen attendees' understanding of their ethical responsibility and accountability as it relates to their role whether it be on the floor or in support of the Manufacturing operation. -
Starting 9 Oct
Single Use Systems for the Manufacturing of Parenteral Products Training Course (PDA 343)
- Oct 9 - Oct 10, 2025
- Bethesda
- , MD
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Starting 3 Dec
Measuring Quality Culture using PDA's Assessment Tool Training Course (PDA 538.3)
- Dec 3 - Dec 4, 2025
- Online