Webinar On Medical Device Single Audit Program (MDSAP)

Description : 

The main goal of the MDSAP is to provide a more effective, efficient and less burdensome regulatory oversight of the quality management systems of medical device manufacturers. The implementation of the MDSAP is intended to allow for a single audit that will satisfy the regulatory requirements of FDA, TGA, Health Canada and Anvisa.

MDSAP includes the use of third party auditors in addition to the regulatory inspectorates. MDASP pilot program started in January 2014 and medical device companies can participate into it on voluntary basis till 2016. After that it will be fully implemented.

Areas Covered in the Session :

What is MDSAP

IMDRF Overview

MDSAP Objectives

MDSAP members

MDSAP Pilot Audit Process

MDSAP Advantages and Disadvantages

MDSAP implementation timelines

Who Will Benefit:

This webinar will provide valuable assistance to regulatory affairs and quality professionals working for or with medical device companies. Professionals who will benefit from this training are in:

Senior Management

Middle Management

Manufacturing

Operations

Consultants

Quality Assurance

Regulatory Affairs

Documentation Department

Quality Auditors

Auditing Organizations

Price Tags:

Live

Single Live : For One Participant

$ 249

Corporate Live : For Max. 10 Participants

$ 899

Recording

Single REC : For One Participant - Unlimited Access for 6 Months

$ 299

For more information and enquiries contact us at

Compliance Trainings

5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada 
Customer Support : #416-915-4458 
Email : support@compliancetrainings.com

For more information on this webinar

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1470

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