Near Miss Report
Near Miss is an unplanned event that did not result in an injury or property damage, but had the potential to do so.
Category: Useful Formats
Quality Manual
A quality manual is a document that states the company’s intentions for operating the processes within the quality management system. It can include policies for…
IQ Protocol
Installation Qualification is defined as, establishing by objective evidence that all key aspects of the process equipment and ancillary system installation adhere to the manufacturer’s…
MSDS Format
It is a document that contains information on the potential hazards (health, fire, reactivity and environmental) and how to work safely with the chemical product.(MSDS…
CVP : Cleaning Validation Protocol
Adequate cleaning procedures play an important role in preventing contamination & cross-contamination. Validation of Cleaning Methods provides documented evidence that an approved cleaning procedure will…
Process Performance Qualification Protocol/Process Validation Protocol
Process Performance Qualification Protocol Name of Product: Stage: Product Code: Plant: Sr. No. Table of Contents Page No. 1. Purpose 2. Scope 3.…
Formats for change control , deviation & categorization of changes.
Excerpt– 1) Do not retain this form and forward to the next after completion of review.2) Put N/A where not applicable.3) Attach an additional sheet…
CAPA Formats- CAPA Request Form & CAPA Register
Corrective Actions and Preventive Actions (CAPA). Download formats from links below- For any Feedback or suggestion, mail at: info@pharmastate.com
SOP on CAPA | Corrective Actions and Preventive Actions in Pharma Industry
Objective : To lay down the procedure of for identification, evaluation, implementation,effectiveness monitoring, closure and documentation of Corrective Actions and Preventive Actions (CAPA). 2.Scope: This…
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