We require experts in medical device regulatory compliance and quality management for European and USA projects. Please contact us through our website if this interests you.
Medical device regulatory and quality management experts required
Related Post
By Mark Wickham | Comments are ClosedAlacramed’s work on the Medical Technologies Science & Innovation Audit (Leeds City Region)(1), sponsored by the Department for Business, Energy and Industrial Strategy, identified technology convergence as being one of the leading drivers in the growthRead more
By Mark Wickham | Comments are ClosedMedtech’s growing influence on pharma By Dr Munna Choudhury, and Dr Mark Wickham, MBA There is no doubt that medtech/pharma deals increasingly appear in the news and that new medtech products and advancementsRead more
By Mark Wickham | Comments are ClosedMark Wickham of Alacramed will be attending Arab Health 2018 in Dubai from 29th January to 1st February. Please contact us if you would like to arrange a meeting.
By Mark Wickham | Comments are ClosedBy Munna Choudhury, PhD Almost 47 million people live with dementia worldwide and it is one of the key causes of disability later in life beating cancer, cardiovascular disease and strokes. This number isRead more
By Mark Wickham | Comments are ClosedThe new EU medical device and in-vitro diagnostics regulations (MDR and IVDR) are due to be in force early 2017 so senior management should be well on the way to formulating a business response. ButRead more
We are a specialist medical device consultancy consisting of industry experts with long and successful track records in commercialising medical device products. We have broad functional and sector experience, and would welcome an opportunity to discuss with you any challenge relating to creating sustainable value from medical technologies.
