Date: | December 3, 2015 - 1:00pm - 2:15pm |
Timezone: | (GMT-05:00) Eastern Time (US & Canada) |
Location: | Compliance Global Inc. 2754 80th Avenue, New Hyde Park, NY 11040, New Hyde Park, NY, 11040, United States |
Website for Event: | https://complianceglobal.us/product/700254/MariaDorat/developing-a-validation-ma... |
Topic: | Distance Learning and E-Learning |
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? How to develop and implement a Validation Master Plan Who Will Benefit Quality Assurance Personnel Level Beginner For more detail please click on this below link: https://complianceglobal.us/product/700254/MariaDorat/developing-a-valid... Email: referrals@complianceglobal.us |
Contact Name: | Compliance Global Inc. |
Contact Email: | referrals@complianceglobal.us |
Contact Phone: | 15169005515 |