Total Pharmaceutical Solution
PROTOCOL FOR VALIDATION OF METHOD OF ANALYSIS FOR CLEANING SAMPLE OF CITALOPRAM HYDROBROMIDE TABLET Superseded Protocol No. Nil Effective Date Table of contents : Sr. …
1.0 Objective 3 2.0 Scope 3-4 3.0 Validation Policy 4 4.0 Introduction 4 5.0 Responsibilities for validation activities 5-7 6.0 Facility description and design 8-9 …
VALIDATION TEAM: Designation Name Signature Date QA Officer Production Chemist Production Manager QA Manager …
PURPOSE: This Sop Describes the Procedure for Validation of shelf life of isopropyl alcohol 70%. SCOPE: This Sop is Applicable to the Procedure for Validation …
Objective To Describe a Procedure for execution of Cleaning Validation Study. 2. Scope This SOP is applicable for execution of Cleaning Validation Study. …
OBJECTIVE To lay down a procedure for minimum requirement for validation or revalidation of manufacturing process applicable to marketed drug products in order to provide …
1.0 OBJECTIVE To lay down the procedure for conducting the hold time study of pharmaceutical products during manufacturing at every stage of In – process …
1.0 OBJECTIVE To lay down a procedure for monitoring Temperature, Relative Humidity. 2.0 SCOPE The SOP is applicable to monitoring the temperature & …
To lay down the procedure for investigation of Out of Specification (OOS) test result(s) of Finished Products, Stability Samples, Raw Materials & Packing Materials etc. …
OBJECTIVE To lay down a procedure to describe the handling of change control which include the procedure for initiation, evaluation, review, approval/ rejection of proposed …
by