Wicham Labs, a contract testing laboratory, announced its upcoming webinar, “Regulatory Changes in Medical Device Development” which will take place on 23rd of May 2018.
Wickham Laboratories Ltd is a GMP / GLP compliant contract testing laboratory that supports the pharmaceutical and medical device industries. Located in Hampshire, England, it was founded in 1962 and remains an independent company. The laboratory has over 50 years of experience and became an established name in the fields of pharmaceutical and medical device contract testing, research and consultancy.
During this webinar, technical experts will provide an overview of the current state of the medial device industry as it consolidates during a time when the market is expanding with unparalleled opportunities for the invention of new devices. They will also cover risk assessments, safety dossier preparation, and any laboratory testing necessary to determine the safety prolife of the device.
As part of the discussion on how these recent changes in registration will affect the companies developing medical devices, webinar will also cover risk assessments, safety dossier preparation, and any laboratory testing necessary to determine the safety profile of the device.
The webinar will be presented by David Small, a medical device consultant at Patient Guard Ltd, a company providing Regulatory and Quality Assurance expertise to Medical Device companies, and Aaron Lloyd, toxicology laboratory manager at Wickham Labs.
Detailed information as well as registration form can be found at the webinar page. Registration is now open for access.