FDA Regulations for Qualification and Validation Processes - 2017
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Website http://www.compliance4all.com/control/w_product/~product_id=501119LIVE?channel=mailer&camp=Webinar&A |
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Category FDA Regulations, to be in compliance with regulatory trainings, medical devices to be in compliance, Qualifications, gamp 5, laboratory manager, clinical laboratory management, quality assurance, fda quality management system, FDA Compliance Training
Deadline: April 27, 2017 | Date: April 28, 2017
Venue/Country: Fremont, U.S.A
Updated: 2017-02-24 19:09:27 (GMT+9)
Call For Papers - CFP
Overview: In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient. Why Should You Attend:The cost of non-compliance is therefore more than that of compliance. Are you in compliance with the FDA regulations for analytical equipment qualification and validation in your facility?Areas Covered in the Session: Requirements and approaches for Analytical Instrument QualificationRisk based validation approachGoing through the qualification phasesUser requirements, writing the specificationsWho Will Benefit:Laboratory managers, supervisors and analystsIT managers and staffConsultantsLaboratory suppliers of material, equipment and servicesSenior quality managersSpeaker Profile: Joy McElroy Upon earning a degree in Zoology at North Carolina State University, Joy made her debut in the pharmaceutical industry in 1992 at Pharmacia & UpJohn performing Environmental Monitoring and Sterility Testing. Her hard work allowed her to move into a supervisory role at Abbott Laboratories where she oversaw their Quality Control Lab.Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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