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Quality & Regulatory Resources
Quality & Regulatory Resources
PDA promotes advances in the industry through strong relationships and dialogue with regulatory authorities around the world through various activities and resources. This page presents the full variety of PDA’s offerings related to quality and regulatory topics, including events and training, associated interest groups, publications, and news items.
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Upcoming Events
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31 Dec
On Demand PDA 578 Technical Report No. 79: Particulate Matter Control in Difficult to Inspect Parenterals
- 31 December 2023 - 31 December 2024 19:00 to 19:00
- Online
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31 Dec
On Demand PDA 592 ICH Q7 GMP for APIs
- 31 December 2023 - 31 December 2024 19:00 to 19:00
- Online
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1 Jan
Technical Report Live! TR-68 (Revised 2024): Risk-Based Approach for Prevention and Management of Drug Shortages
- 1 January - 31 December 2024 7:00 to 8:00
- Online
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12 Sep
PDA 576 Root Cause Investigation for CAPA
- 12 September - 13 September 2024 8:30 to 16:00
- Washington, DC
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16 Sep
PDA 531 Technical Report No. 54-2 and 54-4: Practical Application of Quality Risk Assessment Tools
- 16 September - 18 September 2024 8:30 to 16:00
- Bethesda, MD
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19 Sep
PDA 612.1 Analysis of Environmental Monitoring Data with Respect to cGMP and Data Integrity Guidelines
- 19 September - 20 September 2024 9:00 to 12:00
- Online
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1 Oct
PDA 120 Foreign Particulate Examination, Isolation and Analysis
- 1 October - 2 October 2024 8:30 to 16:00
- Bethesda, MD
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10 Oct
PDA 306 Technical Report No. 65: Technology Transfer
- 10 October 2024 8:30 to 16:00
- Washington, DC
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21 Oct
PDA 569 Drug Delivery Device and Combination Product Risk Management and Safety Assurance Cases
- 21 October 2024 10:30 to 18:00
- Phoenix, AZ
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24 Oct
PDA 450 Learning, Knowledge Management and Impact: Moving from Theory to Practice
- 24 October - 25 October 2024 8:30 to 16:00
- Bethesda, MD
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24 Oct
PDA 211 Quality and Compliance Management for Virtual Companies
- 24 October - 25 October 2024 8:30 to 16:00
- Bethesda, MD
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24 Oct
PDA 546.1 Understanding Container Options and User Needs for Syringes, Cartridge Containers, Wearables and Drug Delivery Systems
- 24 October 2024 10:30 to 18:00
- Phoenix, AZ
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28 Oct
PDA 272 Enhanced Test Methods for Visible Particle Detection and Enumeration on Elastomeric Closures and Glass Containers
- 28 October - 29 October 2024 8:30 to 16:00
- Bethesda, MD
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28 Oct
PDA 247 Fundamentals of Contamination Control, Cleaning and Disinfection Programs for Aseptic Manufacturing Facilities
- 28 October - 29 October 2024 8:30 to 16:00
- Bethesda, MD
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4 Nov
PDA 283 Technical Report No. 43: Identification and Classification of Nonconformities in Molded and Tubular Glass Containers for Pharmaceutical Manufacturing
- 4 November 2024 8:30 to 16:00
- Bethesda, MD
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5 Nov
PDA 417 Introduction to Visual Inspection
- 5 November - 6 November 2024 8:30 to 16:00
- Bethesda, MD
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19 Nov
PDA 620 Technical Report No. 88 Microbial Data Deviation Investigations in the Pharmaceutical Industry
- 19 November - 20 November 2024 8:30 to 16:00
- Bethesda, MD
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19 Nov
PDA 538.3 Quality Culture Assessment
- 19 November - 20 November 2024 9:00 to 12:00
- Online
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3 Dec
PDA Visual Inspection Workshop 2024
- 3 December 2024 3:00 to 11:00
- Berlin, Germany
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3 Dec
PDA 102.3 Technical Report No. 13: Fundamentals of an Environmental Monitoring Program
- 3 December - 5 December 2024 11:30 to 19:00
- Carlsbad, CA
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Related Interest Groups
- Data Governance, Management, Integrity, and Digitalization
- Drug Compounding
- Facilities and Engineering
- Filtration
- Lyophilization
- Management on Outsourced Operations
- Microbiology/Environmental Monitoring
- Packaging Science
- Pharmaceutical Water Systems
- Pre-Filled Syringe
- Process Validation
- Quality Systems
- Regulatory Affairs
- Sterile Processing/Parenteral Drug Manufacturing
- Supply Chain Management
- Technology Transfer
- Visual Inspection of Parenterals
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