Overview
All medicinal products for human use manufactured or imported into Malta and the EU are to be manufactured in accordance with the principles and guidelines of Good Manufacturing Practice (GMP) concerning both production and quality control.
What you'll get
A certificate confirming that a particular establishment is working in line with the EU Good Manufacturing Practice standards
Eligibility
Manufacturers.
How to apply
Fill in the online form, print it, sign it, and send it via email to: inspectorate.adm@gov.mt
Timeline
Submission of Application
Vetting of Application
10 days
Assessment of Application
6 months
Approval of Application
5 days
Delivery of Service
2 days
