Technical Report No. 27, (TR 27) Pharmaceutical Package Integrity
Document status: Active
Technical Report 29, Revised 2012 (TR 29) Points to Consider for Cleaning Validation
Document status: Active
Technical Report 30 Revised 2012, (TR 30) Parametric Release of Pharmaceuticals and Medical Device Products Terminally Sterilized by Moist Heat
Document status: Active
Technical Report 33, Revised 2013 (TR 33) Evaluation, Validation and Implementation of Alternative and Rapid Microbiological Methods
Document status: Active
Technical Report No. 39, (TR 39), Revised 2007, Guidance for Temperature-Controlled Medicinal Products: Maintaining the Quality of Temperature-Sensitive Medicinal Products through the Transportation Environment
Document status: Active
Technical Report No. 39 (Revised 2021) Guidance for Temperature-Controlled Medicinal Products - Maintaining the Quality of Temperature-Sensitive Medicinal Products through the Transportation Environment
Document status: Active
Technical Report No. 3, Revised 2013 (TR 3) Validation of Dry Heat Processes Used for Depyrogenation and Sterilization
Document status: Active
Technical Report No. 41, Revised 2008 (TR 41) Virus Filtration
Document status: Active
Technical Report No. 41, Revised 2022 (TR 41) Virus Filtration
Document status: Active
PDA Technical Report No. 42 - Process Validation of Protein Manufacturing
Document status: Active
