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GMP Quality Templates according ISO 13485 and 21 CFR 820 for Medical Device manufactures and developers.
All templates and forms are in compliance with ISO 13485 ans CFR 820 FDA (USA) and EMEA (European) regulations.
Using one of our standard operating procedure template (SOP template) will save you money and time due to quick and easy adaptation according to your needs.
We provide high quality good manufacturing practice (gmp) documents and templates for the regulated health industry.
ISO 13485 and 21 CFR 820, CFR 4 Standard Operating Procedure Templates – SOPs
Our main expertise is the Quality Management field for drug products, drug substances (active pharmaceutical ingredients, API), medical devices and the ISO regulated industry.
Our Quality Management documents and standard operating procedure templates are built on the industry specific requirements and regulations.
Conformance to ISO 13485 and 21 CRF 820, CFR 4 of our documents is our first goal.
Only 5 minutes to be fully FDA and EMA compliant.
Select, pay, download and implement your high quality document.
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