Checklist for BMR Review
Checklist to review the batch manufacturing record and batch packing record of pharmaceutical products manufactured…
Checklists
Maintenance SOPs
SOP for Air Handling Unit (AHU)
Standard operating procedure for handling air handling unit used for maintenance of cleanliness of the…
HPLC
Difference between C8 and C18 Columns Used in HPLC System
C8 and C18 both types of columns are used in pharmaceutical analysis but their use…
Sterile
Restricted Access Barrier System (RABS) in Pharmaceuticals
Restricted Access Barrier Systems are very useful in sterile pharmaceutical manufacturing to maintain the sterility…
GLP
Importance of Microbiological Analysis in Cleaning Method Validation
Microbial analysis plays an important role in cleaning method validation because the equipment must be…
Validation Protocols
How to Write a Factory Acceptance Test FAT Protocol
Steps to write a factory acceptance test FAT protocol for the equipment purchased for pharmaceutical…
Water System
Water System
These are the articles on  Purified Water System and  Water for Injection (WFI) system to…
GDP
CAPA and Its Proper Implementation
Finding root cause and proper implementation of corrective and preventive action can play an important…
Regulatory
7 Steps for Monitoring Compliance in Pharmaceuticals
Regulatory compliance refers to the process and activities that a company undertakes to ensure that…
Maintenance
Reynolds Number and Its Significance in Purified Water System
Reynolds number is an important factor for purified water distribution system and it helps to…