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
QRM Guidelines
QUALITY RISK MANAGMENT
WHO-Quality Risk Management
Q9-Quality Risk management
Q9(R1)-Quality Risk Management
Format and Content of a REMS Document Guidance for Industry (US-FDA)
Assessment of quality risk management implementation (PIC/S)
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
Calculation of Related Substances by HPLC
September 23, 2012
Hot air oven operation and calibration SOP
June 04, 2023
Types of Blenders in pharmaceutical Applications
January 09, 2023
Solution Stability in Method Validations
September 26, 2012
Disintegration test apparatus operation and calibration
June 04, 2023
Cleaning Validation Calculations-Maximum Allowable Carryover[MACO]
September 29, 2012
Difference between Stability[Shelf life] Specification and Release Specification
September 25, 2012
Calibration of Dissolution Test Apparatus SOP
June 03, 2023
Operation, Calibration and Maintenance of Humidity chamber
November 17, 2022
Enrofloxacin validation in Pure and Veterinary Dosage froms
March 17, 2023
Random Posts
Heating, ventilation and air-conditioning systems for non-sterile pharmaceutical products-WHO
27.12.2022 - 0 Comments
Heating, ventilation and air-conditioning (HVAC) play an important role in ensuring the manufacture of…
Malasia-Guidelines On Good Manufacturing Practice For Traditional Medicines And Health Supplements
23.12.2022 - 0 Comments
The holder of a Manufacturing License must manufacture traditional medicines and health supplements so as to…
Residual Solvents calculation in GC
23.09.2012 - 0 Comments
1.0 OBJECTIVE To lay down the procedure for the Residual Solvents calculation in GC 2.0…
General preventive Maintenance of HPLC
11.11.2022 - 0 Comments
1.0 OBJECTIVE1.1 To have a written procedure for the General preventive Maintenance of…
Multimill Design Qualifications
09.09.2023 - 0 Comments
Multimill Design Qualifications Content:ObjectiveScopeResponsibility (Client and manufacturer)URS (User…
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