Since 2002, Acorn Regulatory has been synonymous with success. In almost 15 years we have never received a rejection from a Competent Authority. That’s a 100% success rate!
Acorn Regulatory is an ISO-certified medical device and pharmaceutical consulting firm that specializes in assisting companies with European regulatory approvals and quality assurance. Our practice areas include:
Our services include:
- Acting as the EU Authorised Representative
- Wholesale Distribution Authorisations
- Advertising Compliance Review of medicinal products
- Resourcing and Outsourcing of Regulatory Affairs Specialists
Acorn Regulatory is headquartered in Ireland. Our team is one of the most experienced and highly regarded regulatory affairs teams in Europe. They have, over the course of their careers, worked on myriad projects for healthcare companies of all sizes. The team continues to grow at our offices in Ireland and with our staff on client sites throughout the world.