SOP for Incident Handling in Pharmaceutical Industry: PharmaState
1. Objective: To lay down a procedure for handling of incidents. Scope: This procedure is applicable for accidental and untoward events occurring in factory premises. Incidents…
Tag: Production
SOP on Calibration Management in Pharmaceutical Industry
Objective: To lay down a procedure for management of calibration procedure. Scope: This procedure is applicable for QC instruments, production equipment, utility service and all other…
SOP for finished product Inspection and Release in Pharmaceuticals
Objective: To lay down a procedure for finished product inspection and release. Scope: This procedure is applicable for all type of finished pharmaceutical product. Responsibility:…
FRIABILITY TEST
(A) Subjective: Procedure for performing Friability test on Tablets. (B) Purpose: This procedure is applicable for friability test on tablets and calibration of friabilator used…
Cleanroom Standards – ISO Guidelines
(A) Background: Before global cleanroom classifications and standards were adopted by the International Standards Organization (ISO), the U.S. General Service Administration’s standards (known as FS209E)…
Procedure for Cleaning and Monitoring of Clean Room Pass Boxes
Cleaning of Clean- Room Pass Boxes: (A) Subject: Procedure for Cleaning of Class- Room Pass Boxes. (B) Purpose: This procedure is applicable for Cleaning of Clean-…
Clean Rooms In Pharmaceutical Manufacturing
A Clean- Room is an environment in which several parameters (like Contamination, Pressurization, Temperature & Humidity and Personnel Access) are controlled, monitored and maintained. Basically…
30 MOST FREQUENTLY ASKED Q&A – ACE INTERVIEWS IN PRODUCTION PROFILES IN PHARMA
Download Full Interview Document: Interview_Pharma Production Q&A PART 1 PART 2 PART 3 For any Feedback or suggestion mail at: info@pharmastate.com
Pharmaceutical Quality/Manufacturing Standards (CGMP)- US FDA
Below is a sortable listing of Pharmaceutical Quality/Manufacturing Standards (CGMP) Guidances CATEGORY TITLE Pharmaceutical Quality/Manufacturing Standards (CGMP) COMPRESSED MEDICAL GASES GUIDELINE Compliance; Pharmaceutical…
Pharma Regulations and Guidelines-India, Easy Access Links
(1). Regulations & Guidelines: CDSCO Central Drugs Standard Control Organization (CDSCO), under MOHFW (Ministry of Health & Family Welfare), Government of…
You must be logged in to post a comment.