PHARMA SOP WORLD
Home
About
Contact
QA
QC
Micro
Prod
Warehouse
Pharmacopoeia
Method Val
Validations
Guidelines
GMP Guidelines
Sterile GMP Guidelines
Stability Guidelines
Cleaning Validation
Quality Risk Management
Method Validation Guidance
Data Integrity
Eng
QA
QC
Micro
Prod
Warehouse
Pharmacopoeia
Method Val
Validations
Guidelines
GMP Guidelines
Sterile GMP Guidelines
Stability Guidelines
Cleaning Validation
Quality Risk Management
Method Validation Guidance
Data Integrity
Eng
Good manufacturing Practices
USFDA 21 CFR part 210 and 211
ICH-Q7 Good Manufacturing Practice Guidance for API
TRS 986 Annexure-2-WHO GMP Guidelines
Health Canada- Good manufacturing Practices
Malasia-Good Manufacturing practices
Hold time studies General guidance
India-Schedule M Good manufacturing practices
Revised Schedule M Guideline-2023
PIC/S-Good Manufacturing Guide part-I
PIC/S- Good manufacturing Practices Part-II
MHRA-Orange Book-Rules and Guidance for Pharmaceutical Manufacturers and Distributors 2017
NAFDAC-Gmp guidelines
Post a Comment
0 Comments
Social Plugin
Search This Blog
Featured post
Microbiology
Sterility Test validation
srikanth nagabiru
September 30, 2023
PROTOCOL APPROVAL Signing of this approval page of protocol indicates agreement with…
Hot Posts
Difference between Stability[Shelf life] Specification and Release Specification
September 25, 2012
SOP for Bacterial Endotoxin Test (LAL Test/BET Test)
May 18, 2025
Qualification of Passbox used in Pharma Industry
October 20, 2023
Solution Stability in Method Validations
September 26, 2012
Resolution Calculation as per EP
September 25, 2012
Limit Test for Iron IP/BP/USP
October 21, 2023
Limit test for chloride
October 16, 2023
Revised Schedule M
May 22, 2024
Dissolution by UV validation test method
December 08, 2022
Disinfectant efficacy validation protocol
January 23, 2023
Random Posts
US FDA - Newly Added Guidance Documents
14.11.2022 - 0 Comments
The Food and Drug Administration (FDA) is responsible for protecting the public health by assuring the…
Hopper Capacity Calculation
05.10.2023 - 0 Comments
The material hopper is an integral part of the feeding system. Typically, it is capable of holding…
Double Door Autoclave Operation, Cleaning and Calibration procedure
06.12.2022 - 0 Comments
1.0 OBJECTIVE To describe a procedure for Operation, Cleaning and Calibration of Double Door Autoclave Make:…
Procedure for the Validation of Analytical Test Procedure for Related substances by HPLC based ICH, USP and Inhouse Guidelines
04.11.2022 - 0 Comments
1.0 OBJECTIVETo lay down the procedure for the Validation of Analytical Test Procedure for Related substances…
Procedure for Technology Transfer
07.11.2022 - 0 Comments
1.0 OBJECTIVE1.1 To lay down a standard procedure for technology transfer to Production department from R…
Categories
AR&D
14
Analytical Methods
51
Data Integrity
4
FR&D
1
Method Validation
18
Microbiology
31
Pharmacopoea
22
Production
51
QA-SOP
70
QUIZ
1
Quality Control
51
Stress Testing
1
Validation
6
Volumetric Solutions
15
books
10
guidelines
46
stability Guidelines
6
stability data evaluation
1
stability studies
1
Contact form
Table of Contents
0 Comments