BioKinetic Europe is as committed to your success as you are. As an independent, flexible Phase I/II clinical pharmacology company made up of talented, dedicated professionals, we have the right approach and experience to help you achieve that success. Our aim is to guarantee that you receive a cost-effective service, on time and within budget.
An enriched working relationship
- Sponsors achieve richer, more meaningful results by tapping into our trial design expertise in Phase I and II studies
- Supplementary accreditation status from the MHRA (UK regulator) confirms our quality service offer
- Regulatory approval with the keenest timeframes in Europe (14 days for Phase 1 CTA) and an excellent working relationship with both the MHRA and REC
- A 7-day turnaround from final protocol to ethics submission
- Studies are filled quickly and easily with our 10,000-strong volunteer database
- Accessible location in Belfast City Centre for clients and volunteers alike
- Sponsors are informed at every point of their trial through our dedicated Project Manager
- Flexibility in utilising sponsor EDC/eCRF system of choice through our extensive experience
- BioKinetic can provide a 2-week timeline from LPLV to database lock
- CRA/Monitor time is minimised with 100% DCF on all source data
- Repeat business from satisfied clients is our number one source of income
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If you would like to learn more about our track record for excellence, please contact us and we will provide information specific to your requirements.
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