Acorn Regulatory has worked on numerous veterinary clinical trials over the years, assisting companies bring new veterinary medicines to the European market. We also support companies at all stages of the licencing process, establishing timelines to market and budget management.
Acorn Regulatory has a Manufacturer’s / Importer’s Authorisation (MIA) licence for Batch Certification of Imported Veterinary Medicinal Products from HPRA.
Our MIA licence enables us to partner with companies to provide them with EU Qualified Person (QP) resource and importation and certification services of veterinary medicinal products in the EU.
We also offer companies the opportunity to avail of our commercial MIA licence to certify veterinary medicinal products for release to the EU Market. We can also support and recommend sites of storage and testing within the EU if required.
MIA Licence: Benefits for you
- Timeline reduction: Developing a QMS and starting the MIA application process can take up to 12 months. Collaborating with Acorn Regulatory will accelerate the lead-time. It is also worth noting that Ireland is the only English-speaking country in the European Union.
- Financial savings: It is financially more cost-effective to contract Acorn Regulatory to provide the required quality services instead of setting up an office and hiring a team of full-time employees in the EU.
- Experience: Acorn Regulatory has a cross-functional team that supports clients every step of the way. Acorn Regulatory employees have extensive industry experience in Quality, Regulatory Affairs, Operations and Supply Chain and have a proven track record of delivering results for clients.
- Flexibility: Our experienced staff will get to know your needs quickly and support your regulatory strategy towards commercial success.