Trade Marks and Designs: Basic Facts

By Inside EU Life Sciences on October 9, 2012

Article originally published in the Briefing paper for the BioIndustry Association on October 9, 2012

Background:
This note provides an introduction to trade marks and designs, from a European perspective. It aims to explain the relevance of trade marks and designs to bioscience companies. It has been prepared by Morag…
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Belgium – Regulatory Overview

By Peter Bogaert on March 5, 2012

Posted in Food & Drug Regulatory, Medicinal Products

Article originally published in the Life Sciences Handbook, 2012

1. What is the regulatory framework for the authorisation, pricing and reimbursement of drugs, biologicals and devices (as they are termed in your jurisdiction)?

Legislation
The main legislative acts regulating medicinal products are the:

Medicines Law 1964.
Royal Decree of 14 December 2006 on Medicines for Human Use and Veterinary Use.
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Inside EU Life Sciences

Trademarks

Trade Marks and Designs: Basic Facts

Belgium – Regulatory Overview

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