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April 12th 2018
We would like to invite you to our latest upcoming webinar, “Regulatory Changes in Medical Device Development” which will take place at 3PM London / 10AM New York, 23rd of May 2018.
During this webinar, our 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. They will also cover risk assessments, safety dossier preparation, and any laboratory testing necessary to determine the safety profile of the device.
Join us to understand the recent changes and their impact on your medical device development portfolio. Registration is now open for access, this and more details about the webinar are located via our landing page here.
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.
As a GMP/GLP compliant laboratory with over 50 years of experience, Wickham Laboratories Ltd is an established name in the fields of pharmaceutical and medical device contract testing, research and consultancy. We conduct business with clients worldwide and the combined expertise of our laboratory technicians and managers enables us to be fully conversant with global regulatory expectations.
We are committed to providing a quality testing service, combining high levels of client satisfaction together with the maintenance of appropriate accreditation. This and the continual pursuit of delivering excellence remain central to our business.
We are routinely inspected by the MHRA, FDA and Home Office, and offer the opportunity for clients to conduct audits on a regular basis.
For more information about Wickham Laboratories Limited and our services, please contact us at +44 (0)1329 226600 or firstname.lastname@example.org. To directly request a company brochure, please visit the Resource Centre section of our company website.