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 MDSAPIMDRF OverviewMDSAP ObjectivesMDSAP membersMDSAP Pilot Audit ProcessMDSAP Advantages and DisadvantagesMDSAP implementation timelinesWho 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 ManagementMiddle ManagementManufacturingOperationsConsultantsQuality AssuranceRegulatory AffairsDocumentation DepartmentQuality AuditorsAuditing OrganizationsPrice Tags:LiveSingle Live : For One Participant$ 249Corporate Live : For Max. 10 Participants$ 899RecordingSingle REC : For One Participant - Unlimited Access for 6 Months$ 299For more information and enquiries contact us atCompliance Trainings5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada  Customer Support : #416-915-4458