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We plan to conduct bioavailability, bioequivalence and various pharmacokinetic studies at our centers in compliance with international regulatory requirements (GLP), strictly monitored by independent quality assurance department from United Kingdom.
As part of support to every stage of the clinical trial, a dedicated project coordinator studies the requirements specific to a trial, designs lab kits, prepares them in a visit-wise shipping container, and labels sample collection tubes along with pre-approved shipping labels and documents. Samples once received are reported within a specified and agreed turn around time.
Centre offers lab services to suit our sponsor`s needs. These range from transferring clinical samples from site to a central lab, to comprehensive project management services. Our services include test design & statistical validity, regulatory consultation, import of kits, reagents, samples, required for clinical research; investigator briefing, providing central lab service and archival.
The information on this page is intended for scientific, educational, and general informational purposes. Clinical approaches, availability, and regulatory status may vary by country, institution, and medical indication. For individual medical decisions, readers should consult qualified healthcare professionals and accredited medical centers.
This article has been prepared by the NBScience editorial team within the scope of clinical research, biotechnology, and international medical information.
