Objective: To lay down the procedure for investigation of out of specification of test results in Microbiology Laboratory. Scope: This Scope is limited to out of specification results of microbial testing, sterility testing and environmental testing in microbiology section of Formulation plant. Responsibility: Head Microbiology Head Quality Control Accountability: Head-Q.A …
Read More »Performance Qualification Report for steam steriliser
Performance Qualification Report for steam sterilizer REPORT APPROVAL Performance Qualification is verified that all test cases required by the protocol are completed, reconciled and included in the qualification summary report. Signatures in the block below indicate that all items in this Qualification Report have been reviewed and found to be …
Read More »Load Pattern & Justification for steam sterilizer
Load Pattern & Justification for steam sterilizer APPROVAL SIGNATURES Signing of this approval page of load pattern indicates agreement with the qualification approach described in PQ protocol. If any modification in the load pattern becomes necessary, a revision through change control shall be prepared, checked and approved. Wherever applicable revalidation …
Read More »Protocol for steam sterilizer and load Pattern
Protocol for steam sterilizer and load Pattern DEPARTMENT PRODUCTION NAME OF THE SUPPLIER MODEL HORIZONTAL-RECTANGULAR SERIAL NUMBER LOCATION VIAL WASHING ROOM EFFECTIVE DATE RUN No. TABLE OF CONTENTS S. No. Description Page No. 1.0 Protocol Approval 2.0 Objective 3.0 Scope 4.0 Equipment Description 2.0 Responsibilities And Identification Of Execution Team …
Read More »US FDA Data Integrity
Data Integrity : The increasingly complex regulatory environments have forced laboratories to adopt a new mindset to compliance and auditing… moving away from traditional instrument validation approaches and consolidating both the instrument data as well as the instrument support across the full spectrum of their lab assets. Contents What is …
Read More »Things to Do When FDA Staff Are on Site to Conduct an Inspection
The 10 Best — and 10 Worst — Things to Do When FDA Staff Are on Site to Conduct an Inspection FDA Expectations • FDA conducts inspections to assess compliance with applicable laws and regulations • FDA expects: – Investigators to conduct inspections in a reasonable manner – Industry to …
Read More »Vendor Qualification
OBJECTIVE : To provide procedure for identification, selection, evaluation and qualification of Raw Material (Active and Inactive) and Primary / Printed Packaging material vendors. RESPONSIBILITY : Head-SCM for identification and selection of Vendor. Head – Quality Control for testing of samples. Head – R&D for taking trial of product batches. …
Read More »Sanitization & Cleaning SOP ( RO )
Chemical Sanitization Procedure for RO first Pass Objective : To Disinfectant the Bacteria in RO membrane Scope :- Procedure : Prepare (0.1 – 1) % Minncare Solution in any solution preparation tank having the capacity of 300 Ltr { Use 300ml of 100% Minncare in 300 Ltrs of Purified …
Read More »Installation qualification for purified water generation system
Installation qualification for purified water generation system Purpose The purpose of this protocol is to provide an outline for the inspection of the system for static attributes to verify that: Each installed sub-component complies with the engineering design and system data sheets/specifications. The system is installed according to the design …
Read More »SOP for sterilization of Miscellaneous Items
SOP for sterilization of Miscellaneous Items Objective: To lay down a procedure for sterilization of miscellaneous Items. Scope: This SOP is applicable for sterilization of Miscellaneous Items. Responsibility: Officers/above (Production-Injectable) is responsible for sterilization of Miscellaneous Items. Accountability: Production Head is accountable for the implementation and compliance of this SOP. …
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