Areas of Expertise

With more than 20 years of  experience in Early Development (Phase I - IIa), Biotrial has successfully managed over 800 clinical studies for the pharmaceutical and biotechnology industry worldwide.

From technically complex trials to the more routine bioavailability/bioequivalence studies, Biotrial has the expertise and capacity to handle all types of clinical projects, including:

• First in Human trials: Single Ascending Dose (SAD) & Multiple Ascending Dose (MAD), Combined SAD/ MAD protocols including food interaction and Proof of Concept/ Bridging studies (POC)

• Late phase regulatory studies: Bioavailability and Bioequivalence studies (BA/BE), Food-Alcohol interaction studies, Age & gender trials, TQTc prolongation studies, Drug-drug interaction studies, Pharmacokinetic (PK) studies and Pharmacodynamic (PD) studies including Imaging (PET, fMRI)

• Vaccine studies

In terms of therapeutic areas, our clinical research experience covers:

• Allergy
• Cardiovascular
• CNS
• Dermatology 
• Endocrinology - Metabolism
• Gastroenterology
• Hematology
• Immunology
• Infectious Diseases
• Oncology 
• Respiratory
• Rheumatology
• Women's health
• etc.

 For more information please contact us:
contact@biotrial.com