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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.
Join PDA TodayUpcoming Events
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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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22 May
PDA 612 Analysis of Environmental Monitoring Data with Respect to cGMP and Data Integrity Guidelines
- 22 May - 23 May 2024 8:30 to 16:00
- Bethesda, MD
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3 Jun
PDA 417 Introduction to Visual Inspection
- 3 June - 4 June 2024 8:30 to 16:00
- Bethesda, MD
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5 Jun
PDA 593 Fundamentals of Automated Visual Inspection
- 5 June 2024 8:30 to 16:00
- Bethesda, MD
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6 Jun
PDA The Future of Drug Delivery Workshop 2024
- 6 June 2024 4:00 to 11:30
- Antwerp, Belgium
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17 Jun
PDA 247 Fundamentals of Contamination Control, Cleaning and Disinfection Programs for Aseptic Manufacturing Facilities
- 17 June - 18 June 2024 8:30 to 16:00
- Bethesda, MD
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9 Jul
PDA 538.3 Quality Culture Assessment
- 9 July - 10 July 2024 9:00 to 12:00
- Online
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23 Jul
PDA 102.3 Technical Report No. 13: Fundamentals of an Environmental Monitoring Program
- 23 July - 25 July 2024 8:30 to 16:00
- Bethesda, MD
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31 Jul
PDA 399.1 Design, Operation, and Qualification of Pharmaceutical Water Systems
- 31 July - 2 August 2024 8:30 to 16:00
- Online
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20 Aug
PDA 109.1 Container Closure Systems and Integrity Testing
- 20 August - 22 August 2024 8:30 to 16:00
- Bethesda, MD
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27 Aug
PDA 802.1 Risk-Based Approach to Airflow Visualization
- 27 August - 29 August 2024 8:30 to 16:00
- Bethesda, MD
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27 Aug
PDA 808 Characteristics of Pharmaceutical Elastomers and Aluminum Seals in Parenteral Packaging Systems
- 27 August - 28 August 2024 9:00 to 17:00
- Middletown, DE
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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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12 Sep
PDA 515 The Impact of CGMPs on Biomanufacturing Facility Design and Operation
- 12 September 2024 8:30 to 16:00
- Washington, DC
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12 Sep
PDA 530 Quality Risk Management: Risk Control and Risk-Based Decision-Making
- 12 September - 13 September 2024 8:30 to 16:00
- Washington, DC
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12 Sep
PDA 529 Technical Report No. 54: Foundations of Quality Risk Management
- 12 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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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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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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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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4 Dec
PDA 399.1 Design, Operation, and Qualification of Pharmaceutical Water Systems
- 4 December - 6 December 2024 8:30 to 16:00
- Online
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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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