PDA TRI Quality and Compliance Events
PDA TRI Quality and Compliance events 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 19 May
GxP Auditing Logistics and Inspection Readiness Training Course (Including Mock Activity) (PDA 298)
- May 19 - May 20, 2026
- College Station
- , TX
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Starting 2 Jun
Quality Management Systems Training Course (PDA 813)
- Jun 2 - Jun 3, 2026
- Bethesda
- , MD
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12 Nov
Measuring Quality Culture using PDA's Assessment Tool Training Course (PDA 538)
- Nov 12, 2026
- Bethesda
- , MD