Technical Report No. 83 (TR 83) Virus Contamination in Biomanufacturing: Risk Mitigation, Preparedness, and Response
Document status: Active
Technical Report No. 84 (TR 84) Integrating Data Integrity Requirements into Manufacturing & Packaging Operations
Document status: Active
Enhanced Test Methods for Visible Particle Detection and Enumeration on Elastomeric Closures and Glass Containers
Document status: Active
Technical Report No. 86 (TR 86) Industry Challenges and Current Technologies for Pharmaceutical Package Integrity Testing
Document status: Active
PDA Technical Report No. 87 (TR 87) Current Best Practices for Pharmaceutical Glass Vial Handling and Processing
Document status: Active
PDA Technical Report No. 88 (TR 88) Microbial Data Deviation Investigations in the Pharmaceutical Industry
Document status: Active
PDA Technical Report No. 89 (TR 89) Strategies for Vaccine Development and Lifecycle Management
Document status: Active
PDA Technical Report No. 90 (TR 90) Contamination Control Strategy Development in Pharmaceutical Manufacturing
Document status: Active
PDA Technical Report No. 91 (TR 91) Post-Approval Change Management and Implementation for Biologics and Pharmaceutical Drug Products — A User’s Guide
Document status: Active
