Exclusive MDR Content
Our expert team has written an extensive overview of the changes that MDR will bring for medical device companies. This exclusive MDR content looks at the changes that device manufacturers, importers, and distributors can expect to have to deal with...
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Download ‘Regulatory Intelligence 6’ Now
‘Regulatory Intelligence 6’ from Acorn Regulatory looks at the latest trends and issues in the sector. You can download your edition of the e-book by completing the form below.
Most Read Acorn Regulatory Publications of 2019
2019 was a busy year for our company when it came to publishing whitepapers and e-books. We looked at issues such as Wholesale Distribution Authorisations, the new medical Device Regulations, Brexit and more. Now, as the year is coming to...
2nd Acorn Regulatory MDR Whitepaper: Be Prepared for May 2021
Our second Acorn Regulatory MDR whitepaper looks at the issues of unique device identifiers, the role of Eudamed under MDR and post market surveillance.
‘PV Update’: Get Our Pharmacovigilance E-Book Now
Acorn Regulatory’s pharmacovigilance and medical teams work with some of the largest and most dynamic companies in the world. They have looked at the major issues impacting their clients at the moment and have created ‘PV Update’ which is our...
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The Acorn Regulatory Newsletter is read by life science professionals around the world every month. We cover the stories that impact on pharmaceutical and medical device regulations.
DEKRA Chosen As 3rd Notified Body Under MDR
DEKRA, the German-based company, has been chosen by The European Commission as the third notified body to be accredited under the Medical Device Regulations (MDR). The new regulations come into effect on May 26th 2020.
Impacted By The LRQA Decision? Here Is How We Can Help
The decisions by Lloyd’s Register Quality Assurance (the LRQA) and QS Zurich that they will both will cease to offer notified body services under the EU’s existing medical device and in vitro diagnostic directives and that they will not seek...
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‘Selected Writing from Acorn Regulatory’ Download It Here
‘Selected Writing from Acorn Regulatory’ highlights just some of the most read articles written by our expert staff in the past 12 months. This e-book is packed with regulatory and pharmacovigilance insights from the team at Acorn Regulatory. Download it...
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Understanding MDR: 8 Important Changes
The advent of the new Medical Devices Regulation (MDR 2017/745) is a cause of much concern for manufacturers and others in the devices sector. The new regulations will bring about many changes compared to the current regulatory framework. We look...
