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The ECJ found that even in cases where consumers do not receive the communication containing claims covered by the Regulation, the communications are in fact aimed indirectly at the consumers.

On January 22, 2015, the General Court of the European Court of Justice held that an orphan medicinal product that has the same therapeutic indication as a previously authorized orphan...

EFSA has launched a public consultation on a draft guidance document on the risk assessment of genetically modified organisms ("GMOs") present at low levels in food and feed material.

On August 11, 2015 the European Medicines Agency ("EMA") released two guidelines on good pharmacovigilance practice ("GVP") for public consultation.

Specifically, ENVI calls for the exclusion of public health services, the REACH law, cloning, bioengineered foods, and the use of hormones in beef.

The EC's proposal applies even when products have been contaminated by GMOs or pesticides that have previously been authorized for use in foods within the EU.

On October 29, 2015, the Members of the European Parliament voted to reject a draft legislation that would enable EU members to restrict or prohibit the sale and use of EU-approved Genetically Modified Organism food or feed on its territory.

On March 11, 2015, the European Parliament signed off on a new law that will break the deadlock and allow new GM crop varieties to be grown in Europe.

On November 16, 2015, Guido Rasi assumed the position of executive director of the EMA. He was appointed following his statement to the European Parliament's Committee on Environment, Public Health and Food Safety last month.

This vote sends the legislative act back to the drawing board.

Additionally, on May 31, 2016, the EC rejected the use of a claim for high-fiber sourdough rye bread in foods for being misleading to consumers.

It is hoped that the amendments to the veterinary agreement will lead to further trade opportunities while reducing costs for exporters.

On April 16, 2015, Regulation (EU) No. 1004/2014 entered into force, setting new rules on butylparaben and propylparaben in cosmetics products.

On April 25, 2017, EFSA issued reporting data for 2016 on pesticide residues in food and feed.

During its October 5–8, 2015, meetings, the Pharmacovigilance Risk Assessment Committee ("PRAC") discussed three ongoing referrals on SGLT2 inhibitors, human papillomavirus ("HPV") vaccines, and Tysabri.

A recently-published study reported that Celltrion's CT-P6 (HERZUMA, trastuzumab-pkrb) demonstrated equivalent safety and efficacy compared with...

All correctly submitted comments will be assessed and, if found to be relevant, taken into consideration by the Scientific Committee in finalizing the guidance.

Antitrust has taken center stage under the Biden Administration, and the Food and Beverage industry has been one of the main targets of increased enforcement by the Federal Trade Commission and Department of Justice, Antitrust Division.