Pharma GMP Document Stamp Tool — FDA · EU GMP · HPRA · Ireland
Add document status stamps (APPROVED, DRAFT, SUPERSEDED, CONTROLLED COPY) to PDFs in your browser. Free, no upload, built for pharma and life science teams.
Upload Pharmaceutical Document
SOPs · Batch Records · Validation Protocols · Regulatory Submissions · QMS Documents
Drop your pharma PDF here
Designed for controlled documents. Apply GMP status stamps (APPROVED, DRAFT, SUPERSEDED, etc.) to any pharmaceutical PDF. All stamping occurs locally — your document never touches any server.
À propos de cet outil
What Is the Pharma GMP Document Stamp Tool?
The Pharma GMP Document Stamp Tool is Ireland's privacy-first PDF stamping solution for pharmaceutical, MedTech, biotechnology, and life sciences teams. It lets you apply standardised GMP document-status stamps — APPROVED, DRAFT, CONTROLLED COPY, SUPERSEDED, FOR REVIEW, GMP COMPLIANT, CONFIDENTIAL, VOID, NOT FOR DISTRIBUTION, and SAMPLE — directly to any PDF inside your browser. No installation. No server. No subscription.
Why Does This Tool Exist?
Regulated companies control documents through their quality management system: each SOP, protocol or record has a defined status such as draft, approved or superseded. A visible status marking on a PDF helps people see that status at a glance, alongside the controls in your document management procedures.
Many stamping tools require uploading the document to an external server. This tool works entirely in your browser, so the document stays on your device. The stamp is a visual marking only: it does not approve a document, act as an electronic signature or make a file compliant with any regulation. Document status is set by your own procedures and systems.
Where Document Status Fits in GMP
Documentation requirements for medicinal products in the EU are set out in EudraLex Volume 4, Chapter 4 (Documentation), and for medical devices in 21 CFR Part 820 and ISO 13485. These require controlled, approved and current documents; how status is shown on a copy, including whether stamps are used, is a matter for each company's procedures. Check your own SOPs before adopting a stamping convention.
Who Uses This Tool?
This tool is designed for professionals working in regulated pharmaceutical and life science environments:
- Quality Assurance (QA) Managers — issuing APPROVED or SUPERSEDED stamps to controlled documents before distribution
- Regulatory Affairs Officers — stamping dossier components as DRAFT or CONTROLLED COPY during review and compilation
- Validation Engineers — marking IQ/OQ/PQ protocols as FOR REVIEW before SME sign-off
- Manufacturing & Operations Teams — receiving CONTROLLED COPY stamped batch records and manufacturing instructions
- Clinical Trial Coordinators — applying CONFIDENTIAL or DRAFT status to investigator brochures and protocol documents
- MedTech / Medical Device Teams — marking status on design and quality documents during review
- Document Control Specialists — maintaining a consistent, auditable visual status system across the QMS
Privacy Architecture
All PDF processing runs entirely inside your browser tab using the pdf-lib JavaScript library, with pages displayed by PDF.js. When you open a PDF, it is read only into your device's local memory. When you place and save stamps, the PDF is modified purely on your device and then downloaded back to your local filesystem. No network request is made for your document at any stage. This is verifiable by running the tool in browser DevTools with the Network tab open — zero requests will appear for your file.
Operated by Priya Life Science, Ireland's life science career and training platform. Read the full GMP document stamping guide →
Comment utiliser
Open the Tool — No Login Required
Navigate to the GMP Stamp Tool. No account, installation, or subscription is needed. The tool runs entirely in your browser.
Upload Your Pharmaceutical PDF
Drag and drop your SOP, batch record, validation protocol, regulatory submission, or any GxP document into the upload zone. The file is loaded into your browser memory only — never transmitted to any server.
Select a GMP Stamp Preset
Choose from 10 standardised GxP presets: APPROVED, CONTROLLED COPY, FOR REVIEW, GMP COMPLIANT, SAMPLE (green/blue) or DRAFT, SUPERSEDED, VOID, CONFIDENTIAL, NOT FOR DISTRIBUTION (red).
Adjust Opacity
Use the opacity slider (30%–100%) to set transparency. A lower opacity keeps the stamp visible without hiding the text beneath it.
Place and Position the Stamp
Click "Place Stamp on Page" to add it to the centre of the current page. Then drag it to any position — top-right corner, page header, or diagonal — to match your site QMS standard.
Stamp Multiple Pages
Use the Previous / Next page controls to navigate through multi-page documents. Add stamps to as many individual pages as your document control procedure requires.
Save and Download the Stamped PDF
Click "Save Stamped PDF". The stamps are drawn into the page content by pdf-lib running locally. Your browser downloads the finished document — no server involved at any point.
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Standard Operating Procedures (SOPs)
Mark SOPs as APPROVED, DRAFT, or SUPERSEDED to reflect the current document lifecycle stage per your QMS. Ensure manufacturing floor copies always carry the correct version status.
Batch Records & Manufacturing Instructions
Stamp batch records, manufacturing instructions, and product dossiers with CONTROLLED COPY or GMP COMPLIANT before issuing to the production floor. Prevents use of uncontrolled document copies.
Validation Protocols — IQ/OQ/PQ
Apply FOR REVIEW or APPROVED stamps to Installation Qualification, Operational Qualification, and Performance Qualification documents before routing for SME and QA sign-off.
Regulatory Submissions (HPRA / EMA / FDA)
Mark dossier components, CTD modules, and submission appendices as DRAFT or CONTROLLED COPY during internal review cycles before final compile for HPRA, EMA, or FDA submission.
Clinical Trial Materials (IB / Protocol / ICF)
Apply DRAFT or CONFIDENTIAL stamps to Investigator Brochures, study protocols, and Informed Consent Forms during development phases.
Medical Device Technical Files (MDR / 21 CFR 820)
Stamp design history files, risk management documents, and device master records during internal review.
Quality Management System (QMS) Documents
Maintain clear version visibility across all QMS-controlled documents including deviations, CAPAs, change controls, and quality agreements.
Training & Education Materials
Mark training documents and GMP awareness materials as SAMPLE or FOR REVIEW to clearly distinguish them from issued, controlled versions during staff training sessions.
Questions fréquemment posées
Does using this stamp make a document GMP compliant?
No. The stamp is a visual marking. Compliance comes from your quality management system and document control procedures, which decide the status of each document and who may approve it. Check your site SOPs before adopting a stamping convention.
Is the stamp an electronic signature under 21 CFR Part 11?
No. A stamp is not an electronic signature and does not provide the audit trail or signature controls that 21 CFR Part 11 requires. For certificate-based signing, see the Digital Signature tool, and assess any tool against your own Part 11 procedures.
Can the stamp be removed or changed later?
The stamp is drawn into the page content, so PDF editing software can alter or remove it. It is not tamper-evident. Keep the controlled original in your document management system.
Does this tool upload my pharmaceutical PDFs to a server?
No. All processing — PDF loading, stamp rendering, and file saving — runs entirely in your browser using pdf-lib and PDF.js. Your document is not transmitted to any server. This is verifiable: open your browser DevTools → Network tab → run the tool — you will see zero requests for your file. Suitable for SOPs, batch records, clinical trial materials, and regulatory dossiers.
What GMP stamp presets are available?
Ten standardised presets are included: APPROVED (green), CONTROLLED COPY (green), FOR REVIEW (green), GMP COMPLIANT (green), SAMPLE (blue), DRAFT (red), SUPERSEDED (red), VOID (red), CONFIDENTIAL (red), and NOT FOR DISTRIBUTION (red). Green is used for active statuses, red for restricted or superseded ones and blue for informational ones.
Can I stamp multiple pages in one document?
Yes. Use the Previous/Next page navigation to move through your document and place stamps on each page as required. All stamps across all pages are compiled and saved together in a single downloaded PDF.
Can I adjust stamp opacity?
Yes. The opacity slider (30%–100%) lets you control stamp transparency so that content beneath the stamp remains readable.
What document types does this tool support?
Any PDF can be stamped: SOPs, batch manufacturing records, validation protocols (IQ/OQ/PQ), regulatory submissions, clinical trial documents, quality agreements, change control records, CAPA reports, deviation reports, technical files, training materials, and product dossiers.
Is this tool free and open source?
Yes. Priya PDF Editor is completely free to use and is open source under the AGPL-3.0 licence. Source code is publicly available on GitHub. There are no accounts, subscriptions, upload fees, or data-sharing arrangements of any kind.
How is this different from just printing and hand-stamping?
Physical stamping requires printing, manual stamping, scanning, and re-filing — adding time, paper waste, and version-control risk. Digital PDF stamps with this tool are permanent, scalable, consistent, auditable (no external server log), and compliant with electronic document management expectations under ICH Q10 and modern QMS standards.