Mondaq All Regions - Belgium: Food, Drugs, Healthcare, Life Sciences
Hogan Lovells
Food product labels are under intense scrutiny from consumers, regulators, class action lawyers, and non-governmental organizations (NGOs).
Hogan Lovells
On April 9, 2018, the Centers for Medicare & Medicaid Services (CMS) released the Benefit and Payment Parameters final rule for 2019 (2019 Payment Notice) applicable to qualified health plans (QHPs) ...
Hogan Lovells
On May 11, 2018, President Trump and Department of Health and Human Services (HHS) Secretary Alex Azar delivered highly anticipated speeches regarding the Administration's plan to reduce drug prices.
Van Bael & Bellis
On 27 July 2015, the Minister for Social Affairs and Public Health, Maggie De Block ("the Minister"), and the pharmaceutical sector umbrella organisations and FeBelGen entered into a "Pact for the Future"...
Jones Day
The Belgian Food Safety Agency recently provided advice on the microbial and chemical safety of insects intended for human consumption.
Field Fisher
In Europa zouden al zeven miljoen rokers de klassieke sigaret gedeeltelijk of volledig hebben ingeruild voor haar elektronische tegenhanger.
K&L Gates GP
The Court of Justice of the EU has recently ruled that EU law allows national authorities to provide the public with information identifying a food business operator whose food is unfit for human consumption even though it is not injurious to human health.
The medical devices sector covers a wide range of products, from simple bandages to highly sophisticated devices such as pacemakers, as well as contact lenses, prostheses, medical equipment for hospital use, etc.
Steptoe & Johnson LLP
Previous editions of EU Analyst have examined how key decisions on EU environment and life sciences regulation are taken behind closed doors. In the EU legal framework, ‘comitology’ committees (made up of a representative from each EU Member State and chaired by the European Commission) simply implement rules laid down by the Council.
McKenna Long & Aldridge LLP
On July 27, 2004, the European Parliament Committee for Environment, Public Health and Food Safety (ENVI COM) will hold its first meeting under the sixth Parliamentary Term.
Hogan Lovells
The 2010 Physician Payments Sunshine Act created a new standard of transparency for financial relationships between pharmaceutical companies and health care professionals in the U.S.
Van Bael & Bellis
Under Article 4 of the Directive, a person injured by a defective product should prove the damage, the defect and the causal relationship between defect and damage.
Van Bael & Bellis
Subject to a few exceptions, EU Member States should apply the national implementing measures of the TPD as from 20 May 2016.
Jones Day
On January 22, 2015, EFSA announced it would make it easier for external observers to attend open plenary meetings by increasing its scientific panels and Scientific Committee open plenary meetings to be held in Brussels.
White & Case
The European Commission's hesitation to provide a legal definition of nanomaterials came to an end last week when its services adopted and released a long-awaited and much-debated recommendation for a regulatory definition for nanomaterials on 18 October.
Van Bael & Bellis
In the midst of the debate over the co-existence of traditional and GM crops, the Court of Justice of the European Union (ECJ) has delivered two very important judgments in the space of a few days.
Howrey LLP
The European Commission has started to consider whether Directive 2001/ 20/EC, better known as the Clinical Trials Directive (the Directive), needs to be revised.
Covington & Burling
May a dominant pharmaceutical company refuse to supply in full the orders it receives from a wholesaler in an EU country in order to limit parallel trade in its products in the European Union?
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Van Bael & Bellis
Under Article 4 of the Directive, a person injured by a defective product should prove the damage, the defect and the causal relationship between defect and damage.
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