Implementing Medical Device Complaint Systems
November 28, 2012 - san francisco CA US

online compliance panel

onlinecompliancepanel1@gmail.com
Phone: 15108575896
Fax: +1-510-509-9659

All medical device manufacturers are required to comply with the complaint handling requirements and medical device reporting (MDR) pursuant to the applicable statutes and regulations. This webinar is intended to help you get familiar with how to implement the medical device complaint handling systems. This webinar is also intended to provide guidance on how to meet the regulatory requirements for handling any complaints concerning all medical device types. Pricing Live Session for one participant Price: $243.00 Corporate Live Session 4 to 10 participants in single location. Price:$986.00 Recorded Session Access recorded sessions only for one participant unlimited viewing for 6 months. Price: $288.00

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