Developing a Validation Master Plan - By Compliance Global Inc.

Expired
Dates : 03 dezembro 2015 » 03 dezembro 2015

Place : Online
Estados Unidos

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Organizer :

Topic : Educação e ensino; Webinar
Ciências da Engenharia;
Keywords: Technology
Description :

Overview

This webinar will provide all medical device companies with a step by step process on how to develop a master validation plan (VMP) for product/equipment transfer, facilities, or to develop a company standard. It will also provide a detailed insight on the best practices for developing and implementing a good plan detailing responsibilities, and deliverables to make validation efficient, and consistent.

Why Should You Attend

Attend this webinar to learn in detail how to develop a VMP and what are the best methods to be followed. The Validation Master Plan describes the way an organization approaches validation; who controls the various aspects of the validation activities; and how production, quality and management will be involved. The VMP also details the validation requirements for each test/ system/ equipment and will guide the organization in achieving its objectives.

Areas Covered in this Webinar

This webinar aims at providing the participants a better insight on: 

  • What is a VMP and how is it valuable to my company?
  • What topics are covered in the VMP and to what extent?
  • How is the VMP controlled and updated?
  • How is the VMP implemented?
  • Who contributes to the VMP?

Learning Objectives

How to develop and implement a Validation Master Plan

Who Will Benefit

  • Quality Assurance Personnel
  • Regulatory Affairs Professionals
  • Operations Staff
  • Engineers 
  • Quality Engineers

 

Level

 

Beginner

For registration:  https://www.complianceglobal.us/product/700254 

About Compliance Global Inc

Compliance Global Inc; is a training (webinar) organization based in New Hyde Park, New York, providing world-class compliance trainings and online webinars by leveraging a pool of experienced speakers / consultants in the Pharmaceutical, Bio-Technology, Medical Devices, Clinical Compliance, FDA Compliance, Healthcare, BFSI, Life Science & HR streams for improving the knowledge base of the customers. Our trainings are contemporary, simple and cost-effective with easy access and great delivery experience. Compliance Global is a multifaceted entity, an absolute knowledge repository.

Our varied industry expertise ranges across Life Science (Pharmaceutical, Bio-Technology, Medical Devices, Clinical Compliance, FDA Compliance), Healthcare, HR Compliance, BFSI, Food & Dietary Supplements, Insurance, Accounting & Taxation and other Cross Industry streams.

Email: referrals@complianceglobal.us

Toll Free: +1-844-746-4244

 

Tel: +1-516-900-5515


Developing a Validation Master Plan - By Compliance Global Inc. to be held in Online, Estados Unidos between 03 dezembro 2015 and 03 dezembro 2015. It covers specific areas of Educação e ensino such as Webinar. Visit the website of the conference for more detailed information or contact the organizer for specific questions.
Add to calendar 2015-12-03 2015-12-03 Europe/London Developing a Validation Master Plan - By Compliance Global Inc. https://www.sciencedz.net/pt/conference/16141-developing-a-validation-master-plan-by-compliance-global-inc Online - Estados Unidos

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