Current Good Manufacturing Practice for Finished Pharmaceuticals
ISO 13485
Medical Devices - Quality Management Systems
ICH Q7
Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
ISO 17020
Conformity Assessment - Requirements for Bodies Performing Inspection
⚠️ Disclaimer: Certifications and capabilities listed are extracted from public databases and have not been independently verified by TSTR.site. We recommend verifying all credentials directly with the testing laboratory and relevant accreditation bodies before engaging services.
🏢 Is this your company?
Take ownership of your testing laboratory listing to manage your profile and receive direct leads.
🏢 Claim This Listing
Are you the owner or representative of this testing laboratory? Claim ownership to manage your listing and access additional features.