CDSCO, EU, EAR, MHRA,TGA, EUDAMED
Pilot, Pivotal,PMS and PMCF
Clinical Trial Management System, eCRF, ePRO,eICF, eTMF
Toxicological Risk Assessment PDE/OEL / ADE Reports Completed 2000 Plus PDE Report
At Bioexcel, we are committed to helping you navigate the complex landscape of clinical trials for Medical Devices.
Our clinical services encompass a wide range of crucial aspects in the development of your Medical Device.
Bioexcel assists clients in preparing thorough and well-documented reports that serve as essential components in the regulatory
Bioexcel’s Scientific and Technical Expertise services offer clients access to a team of highly specialized professionals in various critical fields…
Bioexcel Post-Market Surveillance (PMS) and Post-Market Clinical Follow-Up (PMCF) services are vital for ensuring the ongoing safety and performance of medical devices in the post-market phase…
Guiding Medical Devices to Market Excellence
Bring to the table win-win survival strategies to ensure proactive domination and at the end of the day.
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To support the emerging technology research to get accurate clinical data to diagnose health problem and to deliver value to patients, healthcare systems.
To empower the creators of Medical Devices,guiding them through every stage of development from concept to Market excellence and focus precisely towards the safety of patients for the well being of society
Trust , Team Work , Human Values , Protect & Respect the Human & Animal Subject , Passionate , Integrity , Continuous Development
Client Focused,Flexible And Also Cost Effective.
Clinical studies as per ICH GCP & ISO 14155
Hope for Better Tomorrow
One Stop Solution for Trial Management
TO BREAK THE BARRIERS OF TRADITIONAL CLINICAL INVESTIGATION FOR MEDICAL DEVICE INDUSTRY
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