In the European Union (EU), inspections of medicines manufacturing sites are carried out by national competent authorities from EU Member States. Each year, EU competent authorities and the US Food and Drug Administration inspect many manufacturing sites in the EU, US and elsewhere in the world, to ensure compliance with Good Manufacturing Practice (GMP).
March 13, 2017
On February 20, 2017, Health Canada released the Draft Guidance Document – Drug Facts Table for Non-prescription Drugs for comment.
The threshold for certain pre-closing net benefit reviews under the Investment Canada Act (ICA) and the threshold for a pre-closing merger notification under the Competition Act have been increased for 2017.
What is the rateable value of an unoccupied commercial building that is in the course of being redeveloped or substantially refurbished?
March 10, 2017
Greater outsourcing in German life insurance sector predicted following expected change to Criminal Code
Given the importance of the Quebec market, these changes may have a significant impact on drug manufacturers and wholesalers. In particular, they could affect programs that provide financial assistance to patients and impact certain distribution models for listed drugs.
Essential Corporate News, our weekly news service covering the latest developments in the UK corporate world.
We would like to remind you that according to Article 34 of the Federal Law “On Limited Liability Companies”, every Russian limited liability company is obliged to hold a regular (annual) general participants’ meeting.
March 09, 2017
In the past, concerns regarding news focussed on traditional media (typically newspapers and broadcasters) and the role they played in curating and controlling public information and sentiment.
The NSW Department of Planning and Environment (DPE) has announced proposed amendments to the Environmental Planning and Assessment Act 1979 (EP&A Act), affecting the strategic planning and approvals processes.
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