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.
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