Bioequivalence Studies

MTRL conducts BA/BE studies in accordance with international regulatory standards and is monitored by an independent quality assurance department. We have a large database of over 32,000 volunteers, including healthy and special populations, and female volunteers. We have completed more than 1700 BA/BE Studies and successfully cleared many international (USD FDA, EMA, ANVISA, NPRA etc) regulatory audits. We also have a dedicated volunteer mobilization team to ensure timely completion of studies.

Diagnostics

Our diagnostics services include Biochemistry, Serology, Haematology, Clinical Pathology, and Endocrinology, which are used to diagnose and monitor diseases and conditions.

MTR's molecular diagnostics services include various genetic and DNA tests. These services include Pre-Natal Tests, Post-Natal Tests, Infectious-Test Panels, Pre-Implantation Genetic Testing for Aneuploidies-PGT-A(PGS)Packages, Pre-Implantation Genetic Testing for Structural Re-arrangements and Aneuploidies, Cytogenetic Evaluation, Endometrium Health Packages, and Carrier Screening. These tests are used to identify genetic predispositions to diseases, screen for inherited disorders, and determine if a person is a carrier of genetic mutations that could be passed on to their offspring. MTR's advanced testing and diagnostic services help healthcare providers make accurate diagnoses, offer personalized treatments, and improve patient outcomes. Regenerate response

Regulatory Affairs

Scientific Affairs offers expert data analysis, statistical report writing, and pharmacokinetic analysis services, provided by a team of experienced statisticians, SAS programmers, and medical writers. Their work is done to meet regulatory standards and Our Regulatory Affairs handles IRB submissions and liaises with IRB/IEC. They also communicate with regulatory agencies such as FDA, TPD, and EMEA.