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MHRA ANNOUNCES EARLY ACCESS TO MEDICINES SCHEME

May 6, 2014

On 7 April 2014, the United Kingdom (hereafter “UK”) Medicines and Healthcare Products Regulatory Agency (hereafter “MHRA”) launched the Early Access to Medicines Scheme (hereafter “EAMS”) to provide patients with access to medicinal products that do not yet have a marketing authorisation in the UK.

The EAMS is a voluntary scheme which runs in parallel…

NEW EUROPEAN UNION CLINICAL TRIALS REGULATION ADOPTED ON 14 APRIL 2014

April 15, 2014

EUROPEAN COMMISSION REVISES BLUE GUIDE ON THE IMPLEMENTATION OF EU PRODUCT RULES

March 31, 2014

EUROPEAN COMMISSION PUBLISHES REPORT ON EXTERNAL REFERENCE PRICING FOR MEDICINAL PRODUCTS

March 18, 2014

EMA CLARIFIES NEW VARIATION CLASSIFICATION CATEGORIES

February 17, 2014

UPDATED EMA GUIDANCE ON MAINTENANCE OF INFORMATION REQUIREMENTS

February 17, 2014

IMPLICATIONS OF THE EUROPEAN PARLIAMENT ELECTIONS ON DRAFT LEGISLATIVE PROPOSALS

January 31, 2014

THE COURT OF JUSTICE OF THE EUROPEAN UNION ORDERS THE REVIEW OF AN INJUNCTION BLOCKING THE RELEASE OF CLINICAL STUDY DATA BY THE EUROPEAN MEDICINES AGENCY

December 6, 2013

European Parliament plenary vote on revised medical devices package

October 25, 2013

EMA launches new version of EudraCT

October 22, 2013

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Ciara Farrell

Connect: http://www.hoganlovells.com/ciara-farrell/
Subscribe: Subscribe via RSS
Blogs
  • Focus on Regulation
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  • Hogan Lovells
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