IMed Consultancy Ltd
Specialists in Medical Device Regulations
Sede: United Kingdom
Sobre IMed Consultancy Ltd
We are a highly knowledgeable medical devices regulatory consultancy with key experience in Regulatory Affairs and QA in medical devices, including Class III, active & implantables, Software as a Medical Device (SaMD) and IVDs, founded in 2012. We have a team of skilled medical regulatory professionals offering an outstanding regulatory service. The company offers flexible global regulatory services, supporting businesses in meeting requirements from the UK, EU, USA, and beyond. It acts as an extension of clients' in-house teams, providing services such as UKRP, PRRC, and PMS.
Por que Escolher IMed Consultancy Ltd?
Highly skilled and experienced medical device regulatory professionals
Flexible, scalable, project-based extension to in-house teams
Support with regulatory compliance tasks including PRRC, PMS, UKRP, EUAR
Navigate regulatory challenges and develop compliant solutions
Industry-specific regulatory and client skills
Long-term client retention
Expertise for innovative medical devices globally
Client-focused approach prioritizing needs, timelines, and budgets
Especializações
7+ Serviços
Presença Global
2 Escritórios
Idiomas
1 Idiomas
Mercados
6 Regiões