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Tamara Ghanem

Merrill Brink pharmacovigilance

Pharmacovigilance and adverse event reporting: Five keys for establishing worldwide best practice

Pharmacovigilance, an arm of patient care with a charter to make the best use of medicines and data for the treatment or prevention of disease, is taking on growing importance...

Merrill Brink International

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

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