If you’d like to be regularly informed of the latest developments at Good Manufacturing Practices
1. Site Master File
A Sample for Download
according to PIC/S PE 008-4!
2. Checklist GMP-Inspections
650 questions typically asked during audits
3. Process Validation
official requirements, validation planning and procedure, ...
GMP Compliant Documentation
How to create, organize, review and archive GMP related documents in pharmaceutical industries
Your benefits:
> no shipping costs
> no waiting period: if you choose payment by credit card you will receive an email with the download information immediately after payment.
The pilot project scanned and verified almost 100,000 packs in 25 pharmacies across Stockholm, at the time of dispensing, in collaboration with pharmaceutical retail chain Apoteket AB. Packs from 14 manufacturers were provided with the 2-D data matrix, allowing each pack to be individually identified. The EFPIA solution could provide a valuable asset in reducing the risk of counterfeit medicines reaching patients via the legitimate supply chain.
To read the complete Final Report, check EFPIAs Website
EFPIA/ Announcement
EFPIA/ Joint Final Report