Janine Ross, who recently joined the Mtech Access evidence team as a Consultant Information Scientist, explains how her aptitude for searching and identifying evidence data has earned her the nickname...
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Last month, our evidence team tuned in to watch the Virtually Cochrane conference. Each year the Cochrane conference explores the latest thought leadership in systematic review and healthcare evidence. This...
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Are you looking to launch a new medical technology, medical or diagnostic device in the UK, Europe or North America? Would you like to know how health economic modelling could...
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Challenges for orphan medicines entering the European market – Part 3: Economic evidence development
In this four-part series, we explore the various challenges facing orphan medicines entering the European market and suggest solutions that can help improve patient access. In Part 3 of the...
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Challenges for orphan medicines entering the European market – Part 2: Clinical evidence development
In this four-part series, we explore the various challenges facing orphan medicines entering the European market and suggest solutions that can help improve patient access. In Part 2 of the...
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Shona Lang (Senior Consultant – Systematic Reviews) comments on a recent article in BMJ Evidence-Based Medicine on ‘The need for clinical judgement in the application of evidence-based medicine’1. Having worked...
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Mtech Access attended the virtual World Pharma Pricing Market Access & Evidence Congress on 23–25th September 2020, where our team were inspired by the range of seminars, round tables and...
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We are delighted to announce that Mtech Access has been accepted as a corporate member of the British Healthcare Business Intelligence Association (BHBIA). At Mtech Access, we support our pharma...
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Éanna Connaughton, Senior Medical Writer shares his experiences and perspectives of advisory boards, and highlights some of the other options we offer for those seeking insight from healthcare providers (HCPs). ...
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In order to comply with the EU regulation on medical devices, the regulatory stage Clinical Evaluation Report (CER) has been the focus of renewed attention by the medical device industry....
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