14,474 results found

According to the ECJ, the obligation to disclose this information will allow interested parties to verify whether pricing decisions discriminate between national medicinal products and those originating in other Member States.

The Committee will vote on the final recommendation in July 2016.

The nonbinding resolution made by the Environment, Public Health and Food Safety Committee on January 22, 2015 aims at ensuring more transparency throughout the food chain and restoring public confidence.

On October 26, 2016, Members of European Parliament ("MEPs") resolved to place mandatory limits on industrially produced trans-fatty acids ("TFAs").

The European Federation of Pharmaceutical Industries and Associations and Innovative Medicines Initiative announced the launch of NewMeds new tool for avoiding duplicate enrollment of patients in clinical trials.

French authorities estimate that between 2010 and 2013, 4,700 horses unfit for human consumption were slaughtered and introduced into the food chain.

A German court asked the European Court of Justice ("ECJ") whether Regulation (EC) No 1924/2006 of the European Parliament and of the Council of December 20, 2006.

EFSA has concluded that a comprehensive review of the available scientific evidence shows there is no indication that isoflavones, at levels typically found in food supplements, cause harm to post-menopausal women.

On March 26, 2015, EFSA published a compilation of the monitoring results regarding residues of the pesticide oxadixyl in foods in the EU.

On January 27, 2015, EU Member State experts endorsed a European Commission proposal to establish a list of 77 candidates for substitution...

The Pharmacovigilance Risk Assessment Committee initiated two new safety reviews at its May 2015 meeting.

EMA is calling for statements of interest from experts and stakeholders to attend a workshop on the role of pharmacokinetic and pharmacodynamic measurements in direct oral anticoagulants, scheduled for November 23, 2015, in London.

Registration is open until April 1, 2015, for observers to attend the April 23–24, 2015, plenary meeting...

The PSUR repository is a single, central platform for PSURs and related documents to be used by all regulatory authorities and pharmaceutical companies in the EU.

The European Commission has announced plans to present a new legal framework for the authorization of GMO imports into the EU by the end of April 2015.

On May 24, 2016, The European Commission published a proposal for an annex to the Transatlantic Trade and Investment Partnership ("TTIP") on medicinal products...

The EMA has recommended granting a conditional marketing authorization for Zykadia (ceritinib) for the treatment of adult patients with a type of lung cancer called anaplastic lymphoma kinase positive non-small cell lung cancer.

Last week Bexis published a Legal Backgrounder for the Washington Legal Foundation, entitled "Recent Rulings Establish New Beachheads For Preemption In Drug And Device Product Liability Litigation."