Acorn Regulatory’s Top 100 Articles

Who Will Host The European Medicines Agency?

For those of us working in the sector, the future location of the European Medicines Agency has been a consistent… Read more

Advertising of Medicinal Products

Advertising of Medicinal Products – An Overview

Advertising of medicinal products in Ireland is governed by a statutory instrument (S.I.) 541/2007, which transposes into Irish law Titles… Read more

Authorised Representative EUDR New EU Medical Device Regulations_ The Impact for Economic Operators

CE Marking a Medical Device That Incorporates a Medicine

We are consistently asked about CE marking a medical device.  Our team of medical device experts has written a brief… Read more

Outsourcing Regulatory Affairs

Benefits of Outsourcing Regulatory Affairs

The developments in the market, mergers and the issues associated with pricing pressures applied by governments (such as the IPHA… Read more

Implications of Brexit

The Implications of Brexit for the Life Sciences Sector

The implications of Brexit are still being felt.  Politically, the decision has triggered a chain of events that none of us… Read more

EU GVP

EMA Introduces New Chapter on Good Pharmacovigilance Practices (EU-GVP)

The European Medicines Agency has added a new chapter (Product- or population-specific considerations II: Biological medicinal products) to its guidelines… Read more

Life Sciences Brexit

Brexit Clinical Trials Sector Implications

In this extract from our first Brexit whitepaper we look at the implications of Brexit for the clinical trials sector.

Acorn Regulatory The Implications of Brexit Whitepaper

The Implications of Brexit on the Pharmaceutical, Medical Devices & Clinical Trials Sectors

Acorn Regulatory has published a whitepaper looking at the potential implications of Brexit on a number of healthcare sectors.  The document… Read more

Risk Management Plans

Risk Management Plans – What You Need To Know

To address risk minimisation, healthcare companies are required to have RMPs (Risk Management Plans) in place to document identified and… Read more

Contact us and enjoy a faster, smoother journey through the maze of European Pharmaceutical and Medical Device legislation with us as your expert guide.
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