Overview

 

With state-of-the-art facilities, highly qualified staff and over twenty five years of experience, Biotrial is a leading provider of Non-Clinical Pharmacology services. In addition to GLP safety pharmacology in vivo studies (core battery, supplemental and follow up studies), Biotrial provides specialized efficacy models in the Oncology, CNS, Respiratory and Cardiovascular areas. 

Biotrial is recognized for the excellent quality of its Non-Clinical studies and the expertise of our scientific team ensures the highest quality data for our partners. Biotrial’s scientific and technical expertise is backed up through close contact with well-recognized advisors currently involved in pharmacological and medical research. We can work with you to design and develop experimental models with the highest clinical relevance.

Key Features of Biotrial’s Non-Clinical Services:

 

  • FAST DELIVERY OF HIGH QUALITY DATA

Excellent feedback has been received from our sponsors on the high quality of our data delivered in short timelines.

“Thank you for this thorough and high-quality final report. We appreciate the close communication and flexibility that your group exhibited during the planning and execution of these studies.”

US Pharma Company

 

  • DIRECT COMMUNICATION WITH YOUR DEDICATED STUDY DIRECTOR

At Biotrial we ensure that our sponsors have direct and regular communication with either a dedicated study co-ordinator or with individual study directors.

“Thank you for your careful work on these studies and the timely communications to me. The results are orderly and of high quality.”

US Pharma Company

“We really appreciate the flexibility and communication levels from Biotrial, it is a nice collaboration.”

Japanese Pharma Company

 

  • HIGH QUALITY REPORTS TO MEET YOUR TIMELINES

Biotrial reports have been successfully used by our clients in support of marketing authorization and new product approval submissions around the world. Our dedicated medical writing team produces papers and electronic reports using either the Biotrial template or to your specific technical requirements. Excellently written from the outset, reports can be finalized quickly and efficiently, saving time for our sponsors.

“As like the previous report, very nice work and thorough documentation of the study. It has been a pleasure working with you and your group on these studies.”

US Pharma Company