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Live Webinar Pharmaceutical Quality Risk Management (QRM) Overview

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Website https://worldcomplianceseminars.com/webinardetails/346 | Edit Freely

Category

Deadline: May 02, 2018 | Date: May 02, 2018

Venue/Country: Online, U.S.A

Updated: 2018-04-16 21:19:35 (GMT+9)

Call For Papers - CFP

Live Webinar Pharmaceutical Quality Risk Management (QRM) Overview

Date: 01:00 PM EDT | 10:00 AM PDT | 12:00 PM CDT Duration 60 Minute

Description

Attendees will come away with the ability to recognize the purpose and value of Quality Risk Management QRM, explain the level of risk based on severity, occurrence, and detectability and how the QRM process is used to make decisions. In addition they will be able to identify key QRM terminology and recognize the four (4) key components of Quality Risk Management. Finally they will have a strong understanding of the key concepts associated with the risk management risk tools and their application.

Why should you attend :

Per ICH Q10 Quality risk management is integral to an effective pharmaceutical quality system. It can provide a proactive approach to identifying, scientifically evaluating and Controlling potential risks to quality. However integrating the principles of QRM into our quality processes is complex especially in a pharmaceutical organization. There is much confusion on how to define risk and individuals often think of quality risk management as just a tool like FMEA analysis verses an overall QRM approach. This training will explain the important concepts associated with a QRM approach.

Areas Covered

• Recognize the purpose and value of Quality Risk Management (QRM), as well as how it applies to your job.

• Explain the level of risk based on severity, occurrence, and detectability and how the QRM process is used to make decisions.

• Identify key QRM terminology.

• Recognize the four (4) key components of Quality Risk Management

• Identify examples of QRM tools and their application.

Who will Benefit

• Senior quality managers

• Quality professionals

• Regulatory professionals

• Compliance professionals

• Production supervisors

• Manufacturing engineers

• Production engineers

• Process owners

• Quality engineers

• Quality auditors

• Development professionals

• Senior development managers

Speaker Profile

Expertise: Over 25 years of technical leadership experience in product development, process development, technology transfer, and process optimization. Skilled in taking new products from early laboratory stage to successful manufacturing launch. Expert in integrating Quality by Design and risk management into product development. Experience in establishing a Quality System for a R&D Quality Assurance organization.

Experience: Headed product development departments at Abbott Laboratories and AbbVie Inc. Leadership positions in numerous technical consortiums.

Price: $179 One Dial-in One Attendee | Corporate Live Recorded $279 One Dial In - Max 10 attendees |Group $695 Multiple locations upto 5 dial in | Recorded $249


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.