Pharma Tools
Free GMP Document Stamp Tool for Irish Pharma: Apply APPROVED, DRAFT and CONTROLLED COPY to PDFs Without Cloud Upload
Irish pharma, MedTech and life science teams can now apply GMP-standard status stamps to pharmaceutical PDFs entirely in their browser — with zero file upload, zero server, and full compliance with GDPR Article 25, EU GMP Annex 1, FDA 21 CFR Part 11, and HPRA requirements.
Pharma Tools
Why GMP Document Status Stamps Are a Regulatory Requirement: FDA, EU GMP Annex 1 and HPRA Guide for Ireland
APPROVED, DRAFT, CONTROLLED COPY, SUPERSEDED — these are not just labels. Under FDA 21 CFR Part 11, EU GMP Annex 1, ICH Q10, and HPRA requirements, visible document status marking is a regulatory obligation. Here is the complete guide for Irish pharma and life science professionals.