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- PMLiVE

Merrill Brink

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

Merrill Brink languages

Seven tips to get the most out of your relationships with translation partners

The most effective translation and localization strategies align the best people, processes and technology to deliver multilingual content.

Merrill Brink International

Five steps to choosing the most effective language services partner

Life Sciences Translations – Five steps to choosing the most effective language services partner

Companies in the life sciences industry face a particularly tough set of challenges in bringing products to the global marketplace, not least of which is delivering multilingual content.

Merrill Brink International

- PMLiVE

France ignores EMA and suspends Bayer’s Diane 35

National Agency for the Safety of Drugs and Health Products contradicts PRAC verdict

Bayer symbol

EMA says Bayer’s Diane 35 should remain on European market

Agency investigation concludes acne treatment's benefits outweigh its risks

ABPI publishes updated guidance on pharmacovigilance and digital media

In a guest blog, the ABPI's Esteban Herrero-Martinez explains what changes to European pharmacovigilance legislation mean for ABPI members

- PMLiVE

Black triangle monitoring warning to be used across EU

Use of symbol is part of EMA plans to strengthen pharmacovigilance

- PMLiVE

EMA’s Pharmacovigilance Risk Assessment Committee gains new members

Filip Babylon to represent HCP organisations and Albert van der Zeijden to represent patient organisations

- PMLiVE

New UK guidance on data protection in pharmacovigilance

In a guest blog the ABPI's Esteban Herrero-Martinez sets out some key steps for pharma companies to consider

- PMLiVE

EMA to focus on efficiency, transparency and new legislation in 2013

Regulator also plans significant staff reorganisation

- PMLiVE

EC consults on launch timing for new pharmacovigilance symbol

Wants to know how introduction of 'black symbol' will affect pharma

Roche - Basel

EMA launches probe into Roche’s adverse event reporting

Pharma company allegedly failed to follow pharmacovigilance procedures

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