Wickham Laboratories and Patient Guard have joined forces to host a free webinar on 23 May discussing regulatory changes in medical device development
Wickham Laboratories is a GMP/GLP compliant laboratory with over 50 years of experience in the fields of pharmaceutical and medical device contract testing, research and consultancy. Its latest upcoming webinar, “Regulatory Changes in Medical Device Development”, will take place at 3 pm London / 10 am New York on 23 May 2018.
During this webinar, technical experts will provide an overview of the current state of the medical device industry as it consolidates during a time when the market is expanding with unparalleled opportunities for the invention of new devices.
The panel will also cover risk assessments, safety dossier preparation and any laboratory testing necessary to determine the safety profile of the device.
Registration is now open, and understand recent changes in regulations and its impact on medical device manufacturing.
Disclaimer: Patient Guard Ltd and Wickham Laboratories Ltd are independent companies collaborating on ad hoc projects and the co-presenting of this webinar is not an indication of partnership.