Regulatory and Ethics Submission


It may be the case that your ethics and regulatory submissions can be done in-house but if this is a specific requirement that you need outsourced for UK clinical studies phase II-IV, Klinikos can prepare and submit for UK approval on your behalf.



Klinikos understands the approval system within the UK from Multi-Centre Research Applications down to Site Specific Assessments and can provide information relating to costs and approval timelines.

Ethics and Regulatory Submissions by Klinikos - If you would like more information on our credentials, experience or to discuss your requirements please call us on +44 (0)141 952 1630 or complete our online enquiry form.















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Case Studies

CASE STUDIES

EDC Investigator Training and Recruitment

A Pharmaceutical client required 110 GP Clinical Investigator centres in the UK and Ireland to participate in a long term phase IV risk factor drug study. Klinikos was briefed by the marketing department of the company to identify, select, initiate and monitor the sites.

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TIPS & GUIDES

PDF Download some free templates for use in clinical research trials and improve your efficiency.

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