cGMPs for Medical Devices, Including In Vitro Diagnostic Devices (Medical Devices)
Venue: Online Event
|Event Date/Time: Jun 26, 2012||End Date/Time: Jun 26, 2012|
To achieve sustainability and to remain sustainable and competitive in medical device markets, it is necessary to establish and follow good manufacturing practices (cGMPs) set out in the quality system regulations (QSRs), which help assure that medical devices are safe and effective for their intended use.
Understanding QSRs and the quality requirements can significantly contribute to achieving compliance fast, resulting in saving significant amount of time and efforts and bringing innovative medical products to the market faster.
This webinar will discuss QSRs, requirements and compliance. This session will familiarize participants with the current Good Manufacturing Practice (cGMP) for medical devices including in vitro diagnostic devices. At the end of the webinar, you will get empowered in a way that you would plan, develop, maintain and implement the relevant procedures efficiently and effectively.