SOP For Risk Management. Objective :- The purpose of this SOP is to lay out the procedure for Risk Management (risk identification, analysis, evaluation, reduction / mitigation, communication and conclusion of risk in order to ensure the quality, safety, integrity and purity of the drug product by using FMEA (Failure Mode Effect Analysis). Scope:- The […]
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Good Documentation Practice in Pharmaceutical Industry ( As Per EudraLex Vol- 4) Principle Good documentation constitutes an essential part of the quality assurance system and is key to operating in compliance with GMP requirements. The various types of documents and media used should be fully defined in the manufacturer’s Quality Management System. Documentation may exist
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MANAGEMENT RESPONSIBILITY & CONTINUAL IMPROVEMENT OF PROCESS PERFORMANCE AND PRODUCT QUALITY (ICH Q10) Leadership is essential to establish and maintain a company-wide commitment to quality and for the performance of the pharmaceutical quality system. Resource Management (a) Management should determine and provide adequate and appropriate resources (human, financial, materials, facilities and equipment) to implement and maintain
Before attending any QA&QC interviews be prepared for the below question – Answer QA&QC DEPARTMENT List of all questions asked in interviews of quality control and quality assurance 1 Can any deviation be changed into the change control? 2 What is the difference between Humidity and Relative Humidity? 3 What should be the temperature
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Most Common Interview Questions For Regulatory Affairs Department. 1.What is Regulatory Affairs? Ans-Regulatory Affairs in a Pharmaceutical industry, is a profession which acts as the interface between the pharmaceutical industry and Drug Regulatory authorities across the world. It is mainly involved in the registration of the drug products in respective countries prior to their
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Mastering Change Control in the Pharmaceutical Industry: A Guide to Quality and Compliance Navigate the intricacies of change control with this comprehensive guide! Ensuring the safety, efficacy, and quality of pharmaceutical products hinges on meticulous control over changes. This SOP dives into the essential steps and considerations for implementing an effective change control system in
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Why Self Inspection is Important in Pharmaceuticals industry …? Self inspection is mandatory by Regulatory Authorities like MHRA, EU, and USFDA. It is one of QMS tools to see that Quality of Product is not compromised by any component of manufacturing site. Self inspection should be conducted to check effectiveness & compliance with Good Manufacturing
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Training of employees PROCEDURE: Every employee of the organisation shall first undergo an Induction Training and then to be trained on his / her area of operation prior to start the work. Induction Training shall also include a visit and understanding of works done in Departments other than their own. An Induction Training Record
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