PDA Technical Glossary
PDA Technical Reports are highly valued membership benefits because they offer expert guidance and opinions on important scientific and regulatory topics and are used as essential references by industry and regulatory authorities around the world. These reports include terms which explain the material and enhance the reader’s understanding.
The database presented here includes the glossary terms from all current technical reports. The database is searchable by keyword, topic, or by technical report. Each definition provided includes a link to the source technical report within the PDA Technical Report Portal.
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- TR 54-4: QRM: Biotech Drug Substance (1)
- TR 57: Analytical Method Validation (1)
- TR 66: Single-Use Systems (1)
- TR 67: Objectionable Microorganisms (1)
- TR 68: Drug Shortage Management (1)
- TR 73: Prefilled Syringe User Requirements for Biotech Applications (1)
- TR 85: Enhanced Test Methods - Visible Particle Detection/Enumeration Closures/Containers (1)
- TR 88: Microbial Data Deviation Investigations in the Pharmaceutical Industry (1)
- TR 79: Particulate Matter Control in Difficult to Inspect Parenterals (1)
- Manufacturing (4)
- Packaging Science (4)
- Biotechnology (2)
- Combination Products (2)
- Prefilled Syringes/PFS (2)
- Validation (2)
- Quality Risk Management/QRM (2)
- Filtration (1)
- GMP/Good Manufacturing Processes/cGMP (1)
- Microbiology (1)
- Sterile Processing (1)
- Supply Chain (1)
- Technology Transfer (1)
- Vaccines (1)
- Visual Inspection (1)
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