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Managing Director

Dr. M. Ganesan, Ph.D

Dr. M. Ganesan is the founder and Managing Director of Micro Therapeutic Research Labs Private Limited. He began his career as Trainee chemist in 1993 and became an entrepreneur, set-up his own research and development centre in 2005. He is a Doctor of Philosophy in Applied Sciences from College of Engineering, Anna University, Chennai. Dr. M. Ganesan, first generation entrepreneur, has a multi-role experience in Pharma and Clinical research.

Dr. M. Ganesan is a true visionary. He has a professionally dedicated team of more than 200 scientists, who are involved in the world of innovative healthcare & life sciences. He along with his team of highly skilled scientists had transformed his vision and experiences to the reality of achieving the common goal to serve humanity.

Dr. M. Ganesan is a well-known personality in Pharmaceutical and Biotechnology Industry. He has been a Clinical Research Specialist in India. He had established numerous clinical research laboratories across India, those that meet the stringent GLP and GCP global regulatory requirements.

Principal Investigator

Dr. Madan Kartiya

Dr.Madan Kartiya is an experienced Principal Investigator at a reputed CRO specializing in BA/BE studies. With a Bachelor of Medicine and Bachelor of Surgery degree and three years of clinical experience as a casualty medical officer, Dr. Madan Kartiya possesses the skills and knowledge required to excel in his role. He has a thorough understanding of GCP and GDP practices, which ensures the safety and efficacy of drugs in clinical trials. Additionally, Dr. Madan completed a one-year rotary resident internship that provided him with hands-on experience in patient care and exposure to various medical specialties.

As a Principal Investigator, he oversees the planning and execution of BA/BE studies, ensuring compliance with regulatory guidelines and the production of reliable results. Dr. Madan Kartiya's extensive knowledge and experience make him an invaluable asset to any CRO conducting BA/BE studies, and his contributions to the field of clinical research are poised to benefit the industry for years to come.

He is well versed in GCP & GDP practices and he has undergone one year of rotary resident internship.

QA Manager

Mrs. S. Sathyabama

Ms. Sathyabama S is a highly experienced and organized science professional with a strong background in microbiology, pharmacovigilance, probiotics, food science and safety, drug development, clinical trials, adjuvant immunology, gut microbes, and project management. She has completed her Ph.D in Biotechnology in 2011 and is responsible for ensuring compliance with regulatory guidelines and maintaining quality standards for all aspects of BA/BE studies, including study design, protocol development, data analysis, and reporting. Her extensive experience in project management and quality control has enabled her to successfully lead teams in the execution of BA/BE studies.