Good Documentation Guideline (Chapter 1029 USP) 2018 is a webinar that covers topics such as:
- Chapter outline
- Data collection & recording
- Principles of Good Documentation
- US Pharmacopeia General Chapter 1029
- Purpose of development of this chapter
- History of the chapter as to how and why it was created
- Different types of GMP Documents
- Equipment-related documentation
- Laboratory records
- Batch records
- Deviations and investigations
- Standard Operating Procedure (SOP)*
- Certificate of Analysis (C of A)*
- Analytical procedures*
- Protocols & reports*
- Retention of documents
- Training documentation
Good Documentation Guideline (Chapter 1029 USP) 2018 is intended for:
- Manufacturing & Production Personnel / Managers
- Anybody who works in a Regulated Environment
- Quality Assurance & Quality Control Personnel / Managers
- Research and Development Personnel (R&D) / Managers
- Validation Specialists
- Laboratory Personnel / Managers
- Project Managers
- Clinical Trial Personnel
