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Strategic Alliances

Our carefully chosen strategic alliances allow us to provide additional resources and services for our clients. Providing the full service offer, BioKinetic link with and manage our partners, assuring you a comprehensive, tailor-made solution.

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Almac Group

Almac offers a wide range of integrated services from research, through development to delivery of finished product. BioKinetic Europe work with the Almac site in Craigavon, Northern Ireland, accessing bioanalytical services, including method development, validation and sample analysis. Studies can be performed to meet both US (FDA and EPA) and OECD GLP requirements. Almac is licensed for radio-labelled studies as well as cold material analysis.

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Syne Qua Non

SQN is one of of the largest functional biometrics service providers in Europe with over 17 years experience in supporting international clinical development. They are recognised for their excellence in EDC, Data Management, Statistical Analysis and reporting and are flexible in their approach in meeting clinical development objectives and regulatory requirements in the biometrics arena. Their real-time data collection and reporting EDC environment provides enhanced project management and clinical oversight reporting capability for the clinical and sponsor teams when required.

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3fivetwo Healthcare Ltd.

3fivetwo Healthcare, is a private healthcare provider committed to delivering the highest possible standards of medical excellence within a timeframe that suits their patient. They specialise in a wide range of private services including same day GP, medical consultations in all the main medical disciplines and rapid access to specialist diagnostics such as CT, MRI, Colposcopy, Echo and Treadmill (EST). The 3fivetwo group also encompasses the Sleep Clinic, Origin Fertility Care, Cosmetech and are proud to be the healthcare delivery partners of H3 Health Insurance.

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Eurofins

For more than 20 years, Eurofins Optimed has been offering high quality services in Data Management, Statistics and Medical Writing. In a secure environment, and using the most recent tools (Oracle Clinical®, SAS®, MedDRA, WHO-Drug, CDISC), data from clinical trials are handled and analyzed by experienced and trained specialists. From CRF or e-CRF conception to clinical study report, all the steps are performed in compliance with international recommendations.

 

How does it work?

  • Feasibility & Study Award

  • Regulatory approvals

  • Trial conduct

  • Database lock, review of CSR, study close-out