Dr. M. Ganesan is the Founder and Managing Director of KMS Health Center Private Limited. A Scientist turned an Entrepreneur, set-up his own Clinical Research Centre in 2005 and progressively expanded to Pharma and Biopharma businesses. He is a Doctor of Philosophy in Applied Sciences from College of Engineering, Anna University, Chennai, Tamilnadu. Dr. Ganesan is a first generation entrepreneur and has a multi-role experience in Pharma and Clinical research.
Dr. Ganesan is a true visionary and an accomplished entrepreneur today. He has genuine concerns on public health and is passionated to serve the society with affordable health care and creating more of employment opportunities to the scientific community as well. He has a professionally dedicated team of more than 350 scientists who are involved in the world of innovative healthcare and applied life sciences. He along with his team of highly skilled scientists relentlessly transforms his vision to the reality of achieving the common goal to serve the humanity.
Dr. Ganesan is a well-known personality in Pharmaceutical and Biotechnology Industries. He has been a Clinical Research Specialist in India. He has established a numerous clinical research laboratories across India, those meet the stringent GLP and GCP global regulatory requirements.
Ms. Vasanthi.G holds a degree in MBA from Madras University, Chennai.
She has 16+ years’ experiencein the pharmaceutical industries as BD Executive & BDM.
Ms.Vasanthi works across sectors, and describes her domain as bringing market focus to business strategy. She continues to actively lead the organization in its multi-pronged growth approach for the years ahead.
She is involving in development and implementation of short and long-term strategic marketing and sales plans in line with the organization’s regional & global marketing strategies.
She takes care of project management and has handled more than 20 projects for KMS & has a rich experience of handling more than 850 BA/BE studies.
Ms.Vasanthi leadsan experienced team that is dedicated to the pursuit of meeting our Sponsors' needs while continuing to maintain operational excellence.
She has been a Project Manager for many studies for different therapeutic categories and overseen filing of 3ANDAs for USFDA.
Holds his M.Pharm. degree from Dr. M.G.R. Medical University, Chennai.
He has vast experience in developing injectable and Ophthalmic dosage forms for US, Europe, and Other regulatory.
He is having proven record of successfully delivering numerous scale-up and technology transfer projects during his 15 years professional career.
Holds his Ph.D. degree from Kansas State University, U.S.A.
He has vast experience in developing oral solid dosage forms including osmotic release, extended release and pellet coating formulations.
He is having proven record of successfully delivering numerous scale-up and technology transfer projects during his 15 years professional career.
He seamlessly coordinates with internal departments and clients, consistently exceeding expectations while adhering to international regulations and standards.
Dr. Satyendra Dubey is a skilled pharmaceutical scientist, holds a Ph.D. in Pharamaceutical Sciences.
His expertise spans various dosage forms, including sterile formulations and complex generics.
He is proven leader in cross-functional collaboration, FDA approvals, and patent strategy development.
His contributions extend to nano technology and targeted drug delivery.
With a post graduate degree and over 15 years of experience, he possesses exceptional expertise in analytical development, particularly in the development of solid and semisolid dosage forms.
She holds a Ph.D. degree in Pharmaceutical Sciences focusing research work in the field of Regulatory Affairs and RAC qualified from RAPS, U.S.A.
She has over 18 years of experience and identifies our current regulatory requirement gap analysis & undertaking filings in e-CTD.
She is also involved in due diligence of dossier & developing the regulatory strategy for various markets.
She is highly experienced and organized science professional with a strong background in microbiology, pharmacovigilance, probiotics, etc.,
She is responsible for ensuring compliance with regulatory guidelines and maintaining quality standards.
Her work includes conducting routine internal audits meticulously complying with international regulations and standards.