Incident Report Format | Â Incident Report Template | Incident Report Format For Quality Control Department Incidents | Incident Report HPLC Instrument Malfunction | Â Â
Quality Control Department Incidents – HPLC Instrument Malfunction Read More »
Incident Report Format | Â Incident Report Template | Incident Report Format For Regulatory & Compliance Incidents | Incident Report For Non-compliance observed during self-inspection or regulatory audits | Â Â
Incident Report Format | Â Incident Report Template | Incident Report Format For Warehouse & Logistics Incidents | Incident Report For Wrong material issuance (mix-up in API/excipient/packing material) | Â Â
Incident Report Format | Â Incident Report Template | Incident Report Format For Safety & EHS (Environment, Health & Safety) | Incident Report For Spillage of raw materials, solvents, or intermediates | Â Â
Incident Report Format | Â Incident Report Template | Incident Report Format For Quality & GMP Incidents | Incident Report For Packaging Error (wrong label / misprinted batch number / missing leaflet) | Â Â
Incident Report Format | Â Incident Report Template | Incident Report Format For Quality & GMP Incidents | Incident Report For Deviation from Approved SOPs | Â Â
Quality & GMP Incidents-Deviation from Approved SOPs Read More »
Incident Report Format | Â Incident Report Template | Incident Report Format For Production & Process Incidents | Incident Report For Power Failure / Sudden Line Stoppage | Â Â
Production & Process Incidents-Power Failure / Sudden Line Stoppage Read More »
Incident Report Format | Â Incident Report Template | Incident Report Format For Production & Process Incidents | Incident Report For Equipment breakdown or malfunction | Â Â
Production & Process Incidents-Equipment breakdown or malfunction Read More »
EU GMP Guidelines for Site Master File of Pharmaceuticals | Preparation of a Site Master File of Pharmaceuticals as per EU GMP Guidelines |
Site Master File – EU GMP Read More »
21 CFR Part 211—Current Good Manufacturing Practice For Finished Pharmaceuticals | 21 CFR Part 211 USFDA Guidelines For Pharmaceuticals |
21 CFR Part 211-cGMP Read More »
