The Tick-Tock of the EMA Clock
July 31st marks the final date for submission of proposals by member states to host the European Medicines Agency. Last month, at the EU summit in Brussels, the European Council endorsed a procedure to determine the final location of the...
Sign Up To Receive An Advance Copy Of Our Next Brexit Whitepaper – One Year On
One year on from Brexit we will be looking at the main issues for the regulatory sector. Subscribe to our monthly newsletter and you will receive an advance copy of our next Brexit whitepaper by completing your details below.
Acorn Regulatory Takes Part in British Irish Chamber Trade Mission Event
Acorn Regulatory took part in the first British Irish Chamber Trade Mission ‘Celtic Connection’ to Wales event on June 20th. The event was jointly hosted by the South Wales Chamber of Commerce and the British Irish Chamber of Commerce. The...
Regulatory Affairs Industry News Roundup – June 2017
It has been a busy month at Acorn Regulatory. Here is a recap of the top regulatory affairs industry news stories for the past month. Remember, you can subscribe to our monthly newsletter here and have all of the top Acorn...
Are You Ready for the Falsified Medicines Directive?
The Falsified Medicines Directive (FMD) was published in 2011 with the aim of preventing falsified medicines from entering the pharmaceutical supply chain in the European Economic Area. Conformity with the FMD will be required from February 9th, 2019 next.
SWOT Analysis of the Stockholm Bid for the European Medicines Agency
Stockholm, which we identified at the start of the year as a serious contender to host the European Medicines Agency, remains in contention and has much to offer as the new home to the European body.
Applications To Host European Medicines Agency Must Be Submitted by July 31st
Reports in this morning’s Financial Times (23/05/17) state that applications to host the European Medicines Agency will have to be submitted by July 31st and that a decision on the future location of the agency will be known by the...
Pharmaceutical Regulatory Affairs News – May 2017
It has been a busy month at Acorn Regulatory. Here is a recap of the top pharmaceutical regulatory affairs news stories for the past month. Remember, you can subscribe to our monthly newsletter here and have all of the top Acorn...
Brexit – Moving A Marketing Authorisation
The UK’s decision to leave the EU will cause considerable upheaval for holders of marketing authorisations. As the recognised Brexit experts in the regulatory affairs sector we have some advice and a number of articles to help companies that are...
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5 Steps To Obtain A Wholesale Distribution Authorisation Licence
The WDA process is complex. Indeed, many companies turn to us to manage the application process on their behalf. Here, we have highlighted 5 steps that companies must undertake if they want to secure a Wholesale Distribution Authorisation licence.
