Episode 2- Exploring the Opportunities in Pharma Production and Manufacturing | Humans of Pharma
Episode – 2 | Exploring the Opportunities in Pharma Production and Manufacturing | Humans of Pharma This is Episode 2 of the Career Discussion Series…
Category: Pharma Manufacturing
Oral Liquid Formulations
The oral liquids are homogenous liquid preparations, which contain an emulsion, solution or suspension of one or more active ingredients that are suitable as liquid…
Implementation of Lean Six Sigma in a Pharma Company
Pharma companies implement lean six sigma practices for reducing operating costs and offer the best products to customers. It also enables companies to optimize cost,…
Why Up-Skilling is required in Pharma Industry?
It’s an old saying “Change or DIE” but it holds true in every sense & in all times. Darwin clearly says that Survival of the…
SOP for User Requirement Specification in Pharmaceutical Industry
ObjectiveTo lay down a procedure for User requirement specification (URS). ScopeThis is applicable mainly to production equipment and utility systems. It shall also be applicable…
SOP for Cleaning and Sterilization of Bulk Storage Tank
1. Objective: To lay down a procedure for cleaning and sterilization of bulk storage tank during batch to batch and product to product cleaning. Scope: This…
Validation Master Plan for Pharmaceutical Industry
Author of the document Prepared by Designation: Signature Date: Reviewer of the document for correctness Reviewed by: Designation: Signature: Date: Approver of the document for…
SOP for Computer System Validation in Pharmaceutical Industry
Objective: To lay down a procedure for computer system validation. Scope: This procedure is applicable for all computerized system used in GxP regulated activities. This…
SOP for Failure Investigation in Pharmaceutical Industry
Objective: To lay down a procedure for failure investigation. Scope: This procedure is applicable for investigation of process or system failure having impact on…
SOP for Quality Management System (Documentation) in Pharmaceutical Industry
Objective: To lay down a procedure for origination and review of the Site Master File, Quality Manual, Quality Policy, SOPs, forms and logs. Scope: This…
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