About us - Company Profile
- Founded in 1997
- Specialist medical device CRO
- Service provider to the global medical device market
- Service provider to the global healthcare market
- Adherence to all regulatory requirements, ISO14155, ICH GCP, Clinical Trial Directive, Device Directives, CPMP, EMEA, Competent Authorities throughout Europe and FDA
- Clients based all over the world
- Enviable reputation in the medical device industry
- Client focussed
- Cost effective without compromising quality
- Quality management system in place
- ISO-9001 accredited with BSI
- Investors In People accredited
- MHRA inspected
- High Level of effective communication
- Work to specified timescales
- Training and monitoring services available
- Regulatory services available
- Auditing services available
- Clinical services available
- Statistical services available
- eCRF available
- Data management available
- Staffing and resourcing division
Medvance has built up a very dedicated team of professionals coming from both device and pharmaceutical backgrounds along with a global network of monitors.
Members of this network are extremely experienced and possess the local knowledge needed to ensure that your study is professionally conducted wherever your study sites are.
All the relationships we build with our clients are open, honest, and long-term. Our organisation has a strong emphasis on repeat business and this means meeting our clients' requirements every time we handle a project.
Next step
If you think that we could be of assistance please telephone us and one of our consultants will be pleased to meet with you without obligation or cost.
After the initial meeting we hope you will become a valued client. If not you may still learn something to your advantage and come back to us again in the future.
If you would like to request a proposal then please complete our form.
