Microbiology
Sterility Test validation
PROTOCOL APPROVAL Signing of this approval page of protocol indicates agreement with…
Transporting Tablets
Handling and Transporting Tablets within the Manufacturing Department
1. Purpose To outline the procedure for safe and compliant handling and transportation of tablets within the manufacturing department to ensure pro…
.
Endotoxins
SOP for Bacterial Endotoxin Test (LAL Test/BET Test)
Purpose The objective of this SOP for Bacterial Endotoxin Test (LAL Test/BET Test) is to describe the procedure for accurate detection and quantifi…
.
guidelines
Revised Schedule M
Aimed at ensuring robust quality control for pharma and biopharmaceutical products, the Union Health Ministry on January 6 notified revised rules und…
.
Pharmacopoea
British Pharmacopoeia 2023
The BP 2023 complete package • Six-volume printed edition, including the BP (Veterinary) 2023 • Single-user online licence • Single-user download for…
.
Quality Control
Limit Test for Iron IP/BP/USP
AS PER IP Requirements Nesselar’s cylinder, Measuring cylinder, Glass rod, Citric acid, Thioglycolic acid, Ammonia solution, Standard iron sol…
.
Validation
Qualification of Passbox used in Pharma Industry
Material transfer equipment plays an important role in minimizing contamination risks during the manufacturing process. Avoiding cross-contaminatio…
.
Microbiology
![Difference between Stability[Shelf life] Specification and Release Specification](https://4.bp.blogspot.com/-O3EpVMWcoKw/WxY6-6I4--I/AAAAAAAAB2s/KzC0FqUQtkMdw7VzT6oOR_8vbZO6EJc-ACK4BGAYYCw/w680/nth.png)
Social Plugin