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Belgium
Altius
During this webinar, Kirian Claeyé and Bart Junior Bollen guide you through the eagerly anticipated reform of the reimbursement procedures for medicines in Belgium.
Altius
Belgium is welcoming a significant development in the field of veterinary medicine law. The Act of 11 July 2023 containing various provisions on health, which entered into force on 8 September 2023...
Osborne Clarke
Food label changes for non-UK FBOs | Increasing scrutiny and enforcement for greenwashing relating to food | Uncertainty on food waste reporting...
Altius
Food law is extensively harmonized throughout the EU, but national law still has a role to play. In this short article, we look at three developments in Belgian food law that have taken place in 2023...
Altius
Food law is extensively harmonized throughout the EU, but national law still has a role to play. In this short article, we look at two developments in Belgian food law that have taken place in 2023...
Altius
Both the Belgian legislator and government have played an active role in 2023 when it comes to pharma legislation, which has led to a number of changes...
Altius
On 22 September 2023, the Royal Decree of 13 September 2023 establishing specific rules on the public procurement of biological medicinal products was published in the Belgian State Gazette...
Altius
During this webinar, the experts from our assembled transactions team, Richard Liu, Mieke D'hanis and Pauline Geentjens, provide valuable insights, inform you of common pitfalls...
Altius
On 17 May 2023, the Belgian Medicines Agency (FAMHP) announced that marketing authorisation holders (MAHs) have three years to comply with the prohibition of "negative formulations" on the packaging...
Cooley LLP
Ten medical device and IVD developers will receive free advice on their clinical development strategies from medical device expert panels.
European Union
Osborne Clarke
Advertising, marketing authorisation applications and imports are among the areas targeted by the draft proposals...
Arnold & Porter
On 12 December 2023, the European Commission, the European Medicines Agency (EMA), and the Heads of Medicines Agencies (HMA) published the first version...
Cooley LLP
On 25 September 2023, one year after the publication of the proposal, the European Commission adopted the restriction of intentionally added microplastics under the European Union Registration...
Cooley LLP
The European Commission has adopted Commission Delegated Directive (EU) 2023/1526, which amends Directive 2011/65/EU of the European Parliament and European Council...
Cooley LLP
On 12 July 2023, the European Commission published a factsheet for authorities outside the European Union (EU) and the European Economic Area (EEA)...
Van Bael & Bellis
On 2 May 2023, the Belgian federal Minister of Social Security and Health published a brief policy document defining three proposed action points to deal with medicine shortages in the EU
Cooley LLP
In the EU, medicinal products, medical devices, food supplements and cosmetics are governed by distinctive legislative frameworks.
Timelex
On May 3, 2022 the European Commission released a proposal of the European Parliament and of the Council for a European Health Data Space Regulation.
Cooley LLP
The extension of the transitional periods in the MDR and the removal of the "sell-off" deadline in the MDR and the IVDR were approved by the Council of the EU today.
Cooley LLP
Following the entry into application of the Clinical Trials Regulation (EU) 536/2014 (CTR) for all initial clinical trial applications on 31 January 2023, the European Medicines Agency...
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