Learn all about quality assurance and keep yourself updated by enhancing your skills as a pharmaceutical professional.
The Quality Assurance Department is involved in monitoring quality at various phases of production. According to GMP and Regulatory regulations, all articles will be updated often. Here you will find all types of documents and articles related to quality assurance that are very useful and necessary for all pharmaceutical professionals. All the information on this page is updated regularly. So don’t forget to visit to get all the updated information.
- Cleaning Validation Protocol for Microbiology lab
- Cleaning Validation Protocol for Quality Control
- Cleaning Validation Protocol for Production Area in Pharmaceuticals
- Cleaning Validation Master Plan (CVMP)
- How to Handle Audits in Pharmaceuticals
- Checklist for Reviewing BMR, BCR and BPR in Pharma
- New Best Validation Protocol Writing Techniques 2023
- Pharmaceutical Validation Program
- SOP in the Pharmaceutical industry
- CAPA (Corrective and Preventive Action) in Pharmaceuticals
- APQR Annual Product Quality Review
- SOP for Annual Product Quality Reviews (APQR)
- Common technical document (CTD) Modules
- SOP of SOP in Pharmaceutical