Are you ready for the imminent new medical devices regulations applicable from May 2020?. Implementation of the new regulations needs to be a priority for industry. In less than 10 months, medical device regulations are set to change. With such a short timeline, organisations need to act now to ensure minimal disruption to their organisation and its supply chain.
Medilink WM, in conjunction with Acclaim Biomedical Consulting Ltd. is offering a one day workshop to explore the new European regulations for medical devices including;
By attending this workshop you will:
Meet the expert:
Managing Director Richard Young has an extensive background in regulatory affairs in addition to GMP (quality assurance), GLP (laboratory testing) and GCP (clinical). Spanning over two decades, these core skill areas have been developed with experience in products ranging from class 3 devices such as Orthopaedic implants (IIb) neurological robots, through electromedical devices such as infusion systems and cardio vascular products. Richard brings a blend of pragmatism and experience to these disciplines that facilitates insightful problem solving approaches as well as solid solutions.
Richard’s skills and experience includes such areas as the development and implementation of effective quality management systems, auditing to ISO and FDA QSIT standards, and operating at national and international level through industry associations including Eucomed, ABHI and ABHI Technical Policy Group.
Early bird fee – Register your place before Friday 23 August and receive a 10% discount
Member fee: £180+VAT
Non-Member fee: £215+VAT
To secure your place please contact Zoe Heather at email@example.com or call 0121 452 5630
Invoices will be sent once booking has been confirmed by Medilink WM.