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DTSTAMP:20260523T044401Z
SUMMARY:Webinar on Risk Management for Commissioning and Qualification
DESCRIPTION:Overview: \nAs long as increase in the regulatory require
 ments and market needs which causes conflicts between inspectional par
 ties and manufacturers along with limited resources for each party, th
 ere must be a harmonized baseline between two parties that both must a
 gree on. Upon achieving this harmonization, this will minimize the eff
 orts that will in turn increase the quality of the product.\nAreas Cov
 ered in the Session:\n\nIntroduction to Qualification & Validation and
  discussion the Validation Lifecycl: This part includes introduction f
 or the Validation including (but not limited to) what, why and when to
  Validate? As well as addressing the responsibilities for the validati
 on. Also, this part will discuss the ideal LifecycSle for the systems 
 undergoing the Q&V process so that audience will take good idea where 
 exactly the Risk-Based can play essential role in this cycle.\nIntrodu
 ction to the Risk based Q&V: During this part, there will be discussio
 n about the risk based methodology to be used when qualification/valid
 ation new or existing systems, so that audience will take good idea ab
 out the keys of brainstorming to start implementing acceptable risk ba
 sed approach prior starting the Qualification and Validation activitie
 s, upon implementing this successful and logic Risk-Based approach, th
 is will reflect advantageous outcomes on both compliance and business 
 wises as well.\nCase Study Discussion: Case Study will address the act
 ual and live example that could be discussed to show how risk assessme
 nt is applied for a specific system , case study may include equipment
  or utilities.\n\nWho Will Benefit:\n\nValidation scientists manufactu
 ring supervisors\nEquipment Engineers\nEngineering quality assurance s
 pecialists\nProfessionals from service organizations and vendors who s
 erve pharmaceutical clients\nRegulatory personnel involved in pharmace
 utical industries.\nPharmaceutical Project Manager\n\nSpeaker Profile:
 \n\nMajdi Ayoub is dedicated and results-driven Q&V expert with a hi
 ghly successful background with Pharmaceutical companies in both proje
 ct and operation fields to achieve the best possible performance throu
 gh the creation and execution of successful and creative Q&V strategie
 s. \n\nContact Detail:\nCompliance4All DBA NetZealous,Phone: +1-800-4
 47-9407Email: support@compliance4All.comhttp://www.compliance4all.com/
 Event Link : http://bit.ly/Pharmaceutical_Industry\nLinkedIn Follow u
 sTwitter Follow usFacebook Like us\n\n\n\nFor more information visit h
 ttps://medtechiq.ning.com/events/webinar-on-risk-management-for-commis
 sioning-and-qualification
DTSTART;TZID=America/New_York:20160505T100000
DTEND;TZID=America/New_York:20160505T113000
CATEGORIES:webinar
LOCATION:Online Event
WEBSITE:http://bit.ly/Pharmaceutical_Industry
URL:http://bit.ly/Pharmaceutical_Industry
CONTACT:18004479407
ORGANIZER;CN="Adam Fleming":https://medtechiq.ning.com/profile/Complia
 nce4all
ATTACH;FMTTYPE="image/jpeg":http://storage.ning.com/topology/rest/1.0/
 file/get/2562012364?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Adam Fle
 ming":https://medtechiq.ning.com/profile/Compliance4all
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