Last updated: August 17, 2026
The Scientific-Expert Centre for Medicines created by using nanotechnologies
e-mail: [email protected]
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.
Scientific Case Review
Would you like to understand whether current clinical programs, recent research developments, or emerging approaches may be relevant to your individual situation?
Share your question with our scientific research team and receive information focused on the areas of current research that may be relevant to your case.
- Review of the information you provide
- Relevant research and clinical program information
- A clear response focused on your situation
No obligation. Your question will be reviewed confidentially.
Educational and research information only. This service does not constitute medical advice, diagnosis, prescription, or a personalized treatment recommendation.
