Acorn Regulatory to Present TOPRA Webinar on Northern Ireland Protocol
Janet Fitzgerald, Regulatory Project Manager at Acorn Regulatory, will present on the consultancy approach to the Northern Ireland Protocol in a TOPRA webinar on March 4th at 1.00 pm. The presentation will focus on experiences dealing with the impact of...
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Acorn Regulatory Secures Manufacturer’s/Importer’s Authorisation Licence
Acorn Regulatory has obtained a Manufacturer’s / Importer’s Authorisation (MIA) licence (otherwise known as an MIA Licence) for Batch Certification of Imported Medicinal Products for Veterinary Use.
Download our Clinical Evaluation Report Slide Deck
The most significant change from the MDD to the MDR is the increased focus on clinical evaluation, access to data, and post-market surveillance. This places a greater burden upon manufacturers and their representatives, and it is something that we, at...
Download Our Northern Ireland Protocol Pharmaceutical Guide
How will the Northern Ireland Protocol impact companies in the pharmaceutical sector? That is a question that we have been asked many times in recent months. The issue of the Northern Ireland Protocol has continued to be a source of...
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...
Download Our MDR Changes Slide Deck
The new medical device regulations will be introduced in May 2021. The MDR changes will see an increased set of responsibilities for manufacturers, economic operators, authorised representatives, and distributors. Our MDR regulatory affairs consultants are currently working with companies to...
Sign Up To Receive Our New MDR Newsletter
Acorn Regulatory will launch a dedicated MDR newsletter in January 2021. The time-limited MDR newsletter will be published between January and May 2021 as the medical device sector gets ready for the introduction of the new medical device regulations.
Most Read Explainer Articles of 2020
Acorn Regulatory’s website has a wealth of articles that assist regulatory, pharmacovigilance and clinical professionals all over the world. We consistently feature ‘how-to’ and explainer articles. These are the most read ‘how-to’s’ and explainer articles on our website in 2020.
The Northern Ireland Protocol & Medical Devices: Explained
How will the Northern Ireland Protocol impact companies in the medical devices sector? That is a question that we have been asked many times in recent months. Now, as the UK’s departure from the EU gets closer, we have created...
Most Read Brexit Articles of 2020
Acorn Regulatory has led the way in providing information and assistance to industry professionals since 2016. We have compiled some of the most read and useful articles in one place to help you to better understand how Brexit will impact...
