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 participants 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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Starting 11 Sep
GxP Auditing Logistics and Inspection Readiness Training Course (Including Mock Activity) (PDA 298)
- Sep 11 - Sep 12, 2025
- Washington
- , DC
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12 Sep
Decision-Making in Pharma Manufacturing: Ethics, Compliance, and Resilience Training Course (PDA 297)
- Sep 12, 2025
- Washington
- , DC
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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