Acorn Regulatory is an ISO-certified medical device and pharmaceutical consulting firm that specializes in assisting companies with European regulatory approvals and quality assurance.
|Headquarters|| Suite 6 Powerstown House
Gurtnafleur Business Park, Clonmel, Co. Tipperary, Ireland
1. Since 2002, Acorn Regulatory has been synonymous with success in its field. In almost 15 years, they take pride in never receiving a rejection from a Competent Authority. That’s a 100% success rate! Client testimonials are readily available on our corporate website.
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:
- 2.Pharmaceutical (including regulatory affairs)
- 3.Medical Devices (including regulatory affairs)
- Clinical Trials Services
- WDA Services
- EU Authorised Representative
- Known as eCTD experts.
- PV Auditing
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 Tipperary, Ireland. Their 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 their offices in Ireland and with their staff on client sites throughout the world. The company has 100% compliance with the reporting timelines in relation to the reporting of adverse reactions as individual case safety reports (ICSR) (https://acornregulatory.com/what-we-do/pharmacovigilance/). Routine literature reviews, PV auditing, electronic reporting, and pharmacovigilance training are services offered by their pharmacovigilance division.
Top 5 Recent Tweets
|January 25, 2020||Acorn_Reg||In this edition of 'Regulatory Intelligence' we look at outsourcing for MAH's, post authorisation safety studies an… https://t.co/GgCMNf1y1p|
|January 22, 2020||Acorn_Reg||As part of our series of articles looking at some of the changes on the way for medical device regulation under MDR… https://t.co/pfDtuSVWUK|
|January 22, 2020||Acorn_Reg||Download the 3rd Acorn Regulatory MDR Whitepaper https://t.co/5PqwjGXZi3 https://t.co/3nKf8v5AUF|
|January 20, 2020||Acorn_Reg||In this blog we look at the importance of regulatory strategy. Read more here: https://t.co/5c3TqbNfXC https://t.co/3ro25hygBu|