Buyer guide · 37 pages

Veterinary Medicines Manufacturing Guide

Inside

1. The right product, strength and species. Every batch.
2. Approved record in, released pack out.
3. Which rules reach your product?
4. U.S. drug CGMP: selected duties.
5. EU: the qualified person and the new GMP rules.
6. One production day.
7. Qualified suppliers, specified materials.
8. Receive, sample,
9. Status, retest and expiry.
10. One master record per product, strength, species.
11. Dispense the right lot, in the right amount.
12. Keep products apart.
13. Make it to the record, whatever the form.
14. Sterile products need more.