How to become a Qualified Person
Recommendation
29/30 March 2023
PQR, APR, Management Review, Quality Metrics
Register now for ECA's GMP Newsletter
The European QP Association gets a lot of QP-related questions from its members and from delegates on its events. From time to time the QP Association publishes frequently asked questions and the respective answers on their website (www.qp-association.eu).
Now, selected Q&As are summarised and published in three sets on the public domain of the website. The first set of questions is dealing with topics like:
- How to become a Qualified Person
- Duties and responsibilities of the Qualified Person
- Contract Qualified Persons
- Release Decisions
- Role of the Qualified Person in the Company
Related GMP News
GMP Conferences by Topics
- General Quality Assurance and GMP Compliance Topics
- Hygiene
- General Microbiology Topics
- Regulatory Affairs
- Development
- General Analytics Topics
- Good Distribution Practice
- Sterile Manufacturing
- Computer Validation
- General Qualification/Validation Topics
- General Engineering Topics
- APIs/Excipients
- GMP Basic Training Courses
- Medical Devices and Combination Products
- Packaging and Packaging Material
- Data Integrity
- Qualified Person (QP)
- GMP Auditing
- Documentation
- Cleaning Validation
- General IT Compliance Topics
- Impurities
- OOS / OOE / OOT
- Material Testing
- Validation of Analytical Methods
- Analytical Instrument Qualification
- Stability Testing
- Microbiological Testing
- Technology
- General Manufacturing Topics
- Solid Dosage Forms/Semi-Solid Dosage Forms
- Biotechnology/Blood/ATMP
- Herbal Drug Products/Cannabis/Radiopharmaceuticals
- Others