Best Practices for Quality Risk Management for Pharmaceutical Industry
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Website https://compliance2go.com/product/?pid=CP2014-391 |
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Category Biotechnology , Pharmaceutical
Deadline: November 13, 2014 | Date: November 13, 2014
Venue/Country: Houston, U.S.A
Updated: 2014-11-01 16:02:09 (GMT+9)
Call For Papers - CFP
DESCRIPTIONFirms in pharmaceuticals including those manufacturing biosimilars and biologics, who are intending to bring products into the US market, are subject to quality risk management (QRM). This presentation is intended to help you get familiar with best practices for the QRM applicable for pharmaceutical industry (drugs, biosimilars, and biologics).This seminar is further intended to discuss how quality risk management can be effectively integrated into a quality system (QS) in the pharmaceutical industry.This seminar will help attendees understand risk management principles, risk management tools, methods and processes applicable to the pharmaceutical industry. In addition, this seminar will help the attendees how to develop and implement a systematic and holistic risk management strategy integrated into the quality system.This 60-min webinar will provide great opportunities for you to get familiar with the details of how to implement the systematic and holistic quality risk management for drugs, biosimilars and biologics. Why should you attend :This webinar is intended to help you learn and ensure you can adequately implement quality risk management (QRM) applicable for pharmaceutical industry (drugs, biosimilars, and biologics). Areas Covered in the Session:Laws, Regulations, Rules and/or StandardsDefinitionsRisk Management (RM) Process ? Systematic and IntegratedRM PrinciplesRisk Management Tools and MethodsRisk RankingHow to Facilitate Quality Risk ManagementCommon Mistakes and How to Prevent Common PitfallsRisk Control MeasuresRisk Communication ? HowRM Applications for Operations, R&D, Materials, Facilities, Utilities, Equipment, Manufacturing, Labeling and Packaging, Laboratory Studies and Quality Control.Doing RM Right Without Wasting ResourcesPractical Aspects (Value) of Risk ManagementRelationship with Other Quality SubsystemsCommon Pitfalls and MisconceptionHow to Avoid Common MistakesImplementing RM in an Efficient and Effective Manner.Speaker’s Practical PASS-IT Guide? Who will benefit: (Titles)CEOsVPsCompliance officersAttorneysClinical affairs (associates, specialists, managers, directors or VPs)Regulatory affairs (associates, specialists, managers, directors or VPs)Quality assurance (associates, specialists, managers, directors or VPs)R&D (engineers, scientists, managers, directors or VPs)CROsConsultantsContractors/subcontractorsWebinar Includes:Q/A Session with the Expert to ask your questionPDF print only copy of PowerPoint slides60 Minutes Live PresentationCertificate of Attendance
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