Our Key People

Dr. M. Ganesan - Ph.D

Managing Director

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,Guindy,Chennai.

Dr. M. Ganesan, first generation entrepreneur, has a multi-role experience in Pharma and Clinical research. He is a well-known personality in Pharmaceutical and Biotechnology Industry.

He has been a Clinical Research Specialist in India. He had established numerous clinical researchlaboratories across India, those that meet the stringent GLP and GCP global regulatory requirements.

Dr.Kanthi Shankar

Principal Investigator

Dr. Kanthi Shankar holds an MS in Clinical Research from the University of South Carolina, USA, and boasts 25 years of extensive medical expertise, including 11 years dedicated to leading BA/BE Studies. As Principal Investigator for a BA/BE center, she has overseen numerous oncology trials and efficacy studies on skin ointments. Her role as a medical consultant and reviewer has been bolstered by certifications in CITI, ICH-GCP, and extensive training in SAS and pharmacovigilance.

Dr. Shankar's contributions extend to two published research papers, highlighting her significant impact in advancing clinical research methodologies and outcomes.

Ms. Revathy

Project Manager

Ms. Revathy is a well-qualified and experienced professional with a background in Clinical Research and Pharmacy, having worked in various roles including Project Manager. She is skilled in GCP compliance, monitoring, and regulatory guidelines, with a dedication to quality work and subject safety. Her expertise extends to clinical trial management in bioequivalence and bioavailability studies, ensuring adherence to study protocols and regulatory standards.

She has successfully handled over 60 projects in bioequivalence and bioavailability studies in hospital settings, demonstrating proficiency in overseeing clinical operations, data management, and report generation.

Mr. Deepak Pabale

Bio Analytical - Head

Mr.Deepak Sadashiv Pabale, an accomplished Deputy Manager / Manager in R&D, Bio-Analytical Department with over 18 years in the pharmaceutical sector. M.Sc. in Analytical Chemistry, adept in method development, validation, and study sample analysis. Expertise in GLP compliance, SOP implementation, and managing laboratory operations with a track record in regulatory audits including USFDA and MHRA.

He is experienced in managing GLP and statutory compliances, optimizing processes, and leading audits successfully.

Dr. Veerabhuvaneswari

Medical Writing

Dr. Veerabhuvaneshwari V is a seasoned medical and scientific writer with over 8 years of academic experience and 3 years in pharmaceutical R&D, focusing on oncology, inflammation, and toxicology. A Gold Medalist in M.Tech Biopharmaceutical Technology with a submitted Ph.D. in Biotechnology from Anna University, she brings deep expertise in drug discovery, assay development, and regulatory documentation. Her core strengths include pharmacovigilance, QC/QA, and scientific communication, backed by a Lean Six Sigma Black Belt and multiple certifications in clinical research and medical writing.

She has authored 24+ peer-reviewed publications, contributed to grant-funded research, and holds two patents in novel device technologies. With a proven track record in scientific writing, regulatory submissions, and organizing knowledge exchange platforms, Dr. Veerabhuvaneshwari excels in translating complex data into impactful, regulatory-compliant content for global healthcare audiences.

Ms.Padmini

QA Manager

Ms. Padmini Ethirajan is an accomplished QA professional with over a decade of focused experience in bioanalytical operations supporting BA/BE studies for regulated markets. With an M.Tech in Biopharmaceutical Technology from Anna University, she has deep expertise in method development, validation, and sample analysis aligned with USFDA, ANVISA, and MoH guidelines—ensuring regulatory compliance at every stage of BA/BE study execution.

Currently serving as the Head of QA, she oversees end-to-end quality systems for bioanalytical method validation, clinical sample processing, and analytical data review. Her proficiency in LC-MS/MS platforms, GLP practices, and audit preparedness ensures data integrity and operational excellence in BA/BE studies from protocol to submission.