Download Our Repeat Use Procedure Slide Deck
The issue of Repeat Use Procedures generates many questions to our pharmaceutical regulatory affairs team. We have created a slide deck looking at the main points to consider when completing a Repeat Sue Procedure. You can download it below.
Download Regulatory Intelligence 10 from Acorn Regulatory
Regulatory Intelligence 10 from the award-winning experts at Acorn Regulatory looks at issues from the pharmacovigilance, medical devices, clinical and pharmaceutical sectors. You can download your copy of the latest guide in the Regulatory Intelligence series by completing the form...
How Will The Northern Ireland Protocol Impact Medical Device Companies?
Our clients have been contacting us in recent weeks with questions relating to the Northern Ireland Protocol and medical devices. They are eager to understand the intricacies of the Northern Ireland Protocol and how it will impact their companies. We...
Download ‘Regulatory Intelligence 9’ from Acorn Regulatory
‘Regulatory Intelligence 9’ from Acorn Regulatory has a wide range of articles covering issues such as Brexit, the new Medical Device Regulations, DCP Close Outs, and more. The articles in ‘Regulatory Intelligence 9’ have been written by members of our...
The Acorn Regulatory Brexit Guide No. 1 Revised for 2020
We published our first Brexit guide in July 2016. Back then, we looked at the potential implications for the life sciences sector. Now, we know much more about how Brexit will look at the moves that companies need to take...
Preparing for a No Deal Brexit – The 9th Acorn Regulatory Whitepaper
The seemingly never-ending Brexit negotiations have continued throughout the pandemic. Talks initially held virtually, have now progressed to face to face meetings. While the format of the meetings might have changed there has been little progress to report as both...
Download Our Drug-Device Whitepaper
The new MDR has significantly updated the requirements for medical devices placed on the European market. It has introduced new requirements for manufacturers to comply with to achieve CE marking before placing their products on the European market. Some of...
Download Our Clinical Trials E-Book
Acorn Regulatory is a leading regulatory, pharmacovigilance and clinical consultancy company headquartered in Ireland. Our Clinical & Medical team works with the largest and the leading companies in life sciences to assist them in bringing their products to market. The...
Download our CMC e-book Now
Acorn Regulatory’s team of CMC, pharmacovigilance, quality, clinical and medical devices experts consistently produce articles for the sector. In the CMC e-book, we have compiled some of the most-read articles into a downloadable PDF. In this CMC e-book, we will...
Acorn Regulatory’s Essential Publications
In recent years, we have produced over 25 well-regarded publications. We have looked at topics as diverse as Brexit, CMC, Clinical Trials, Medical Device Regulations and much more. Here, we have compiled a list of the most-read publications for you...
