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Ensuring you are EU Medical Device e-labelling compliant - A best practice strategy

Ensuring you are EU Medical Device e-labelling compliant – A best practice strategy

The EU Directive No 207/2012 on electronic labelling for Instructions for Use (IFUs) for certain medical devices was adopted effective March 9, 2012.

Merrill Brink International

Google taps ex-Genentech CEO to lead its new health company

Says Calico will have particular focus on diseases associated with ageing

- PMLiVE

Hikma pushes further into Africa with Ethiopian JV

Forms alliance with MIDROC to create HikmaCure

- PMLiVE

US NIH provides $45m for Alzheimer’s research

Projects will investigate basic science of the neurological condition

- PMLiVE

GSK hands back rights to ChemoCentryx drug

Investigational IBD treatment vercirnon disappoints in phase III

- PMLiVE

CDM Group re-brands non-US businesses

Develops platform for agencies to focus on growth

- PMLiVE

Online doctor collaboration demonstrates value

Developer says web and mobile app iConsult has helped diagnose thousands of cases

- PMLiVE

EMA’s Paediatric Committee elects new leaders

Dirk Mentzer and Henk van den Berg elected as chair and vice-chair

- PMLiVE

FDA to review AZ’s fish oil drug Epanova

Hypertriglyceridaemia treatment acquired as part of Omthera takeover

- PMLiVE

Teva signs R&D alliance to pursue novel cancer drugs

Will work with Cancer Research on first-in-class oncology treatments

- PMLiVE

Ethan Knowlden leaves Novartis for Complete Genomics

Joins genome sequencing firm as senior VP, general counsel

- PMLiVE

Delivering ‘beyond the pill’

Communicating added value is now crucial for market access programmes

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