Mr. Chakrapani holds a Master's in Pharmaceutical Sciences with a specialization in Pharmacology, Pharmaceutical Analysis, and Biostatistics.
He comes with 22+ years of collective Operations and Quality Assurance experience working for various pharmaceutical companies and CROs including Veeda CR, Greensyn Lifesciences, Panexcell, Novartis, Ranbaxy, Zydus Cadila, USV and Lambda. His experience spans from Bioequivalence studies, Phase-1 to Phase-4 Clinical trials to techno commercial management of CROs.
He has an accomplished Quality Assurance career and rich experience of facilitating more than 50 Regulatory inspections from various regulatory bodies including USFDA, UK-MHRA, WHO, ANSM, ANVISA, AGES, MCC, NPCB, GHC, DCGI, etc. His success stories include, setting up of complete QMS and integration of various Global establishments of Veeda CR in India, Malaysia, Belgium, France, USA, and UK.
As COO of JSTL, he is responsible for overall business, achieving sustainable Operational and Compliance Objectives of the organization.
Mr. Jeevan Krishna Kuchipudi is the CEO & Executive Director of Enhops Solutions Private Limited & Enhops Inc. As a passionate entrepreneur, Jeevan has diverse global experience, exceptionally in IT and Finance. He is constantly engaged with development of new products through his out of the box and consumer intensive ideas.
Jeevan holds an MBA in Finance from San Diego State University. Through his academic and career moves, Jeevan has showcased the vision to be an all-encompassing team leader as well as a team player. He embraced progressive skills in various segments which include Software Development, Quality Assurance, Financial Analysis, Business Analysis, and Project Management. Jeevan played active roles in finance, credit, insurance, technology and healthcare domains while working for giants like Core Logic Credco, Boingo Wireless, Humana, Tata Consultancy Services and Jeevan Softech Limited.
Mr. Naidu is Vice President - Operations at Jeevan Scientific Technology Limited (JSTL) and having more than 20 years’ of professional experience in Clinical Research and Pharma Companies. He has been associated with JSTL since 2014. Before joining JSTL, he was associated with Azidus Laboratories, Actimus Bio, RA Chem Pharma in heading different portfolios including Clinical, Bioanalytical and Quality Assurance.
He has a successful track record in handling of BA/BE operations and CT management and excellence in technical, client relationship management and people management skills.
He has played a significant role in the development, implementation of Quality Management Systems in several CROs and making them of global standards. He also has rich professional experience in handling various regulatory inspections USFDA, WHO, ANVISA, MHRA, MoH Turkey, NPCB, CAP, NABL, and CDSCO.
Mr. Naidu is responsible for organizing and implementing operational strategies for all BA/BE studies at Jeevan Scientific.
Mr. Ravi Vadlamudi is head of Bioanalytical Research at Jeevan Scientific.
Mr. Ravi has a rich experience of more than 15 years in the field of clinical research. He is expertise in organizing, developing and implementing technical strategies in bioanalytical research especially handling large molecules.
Prior to Jeevan Scientific, he was associated with Lupin Bioresearch Center, Lambda Therapeutics, Admerus Biosciences, and RA Chem Pharma with vast experience in handling complex folios Contraceptives, Endogenous compounds, Vitamins, Steroids, hormonal drugs, synthetic hormones, corticosteroids, Nasal Spray, Inhalation products and peptides. He has hands on experience in handling end to end operations in BA/BE studies. He also has professional experience in facing different regulatory audits USFDA, MHRA, AFSSAPS and CDSCO. He is a professional with technical, people management and client relationship skills.
Mr. Ravi is responsible for overall Bioanalytical Research activities in JSTL.
Dr. K. Someswara Rao as Vice President - Clinical Research heads the Clinical Trials department at Jeevan Scientific Technology Limited (JSTL) and is also responsible for organizing and implementing operational strategies for the entire company. He has been associated with JSTL since January 2022 and has more than 19 years of professional experience in Clinical Research and Pharma Companies. Before joining JSTL, he was associated with AXIS Clinicals Ltd, Emcure Pharmaceuticals, Ranbaxy Laboratories, Sun Pharma Advanced Research Centre and Dr. Reddy's Laboratories Ltd., heading different portfolios including clinical pharmacology and biopharmaceutics, pharmacokinetics and biostatistics, medical wiring and clinical research.
Dr. K. Someswara Rao has vast experience in conducting many clinical trials in various therapeutic segments including Oncology, Schizophrenia, Diabetes, Ophthalmics, Arthritis, Diarrhoea, Dermatology, Vaccines, Vasoconstrictor studies, Transdermal Patches, Narcotics, Asthma and Biosimilars, while working in several CROs and Pharma companies and played significant role for the market entry. He has vast experience in conducting bioavailability/bioequivalence studies for orals and other several pharmaceutical dosage forms like Nasal Sprays, Suspensions, Dispersible Tablets, Gels, Creams, Lotions, Ointments, Transdermal Patches, Chewable Tablets, Intravenous or Intramuscular Depot Injections, Liposomal Injections, Skin Irritation and Sensitization studies, Adhesion studies and Narcotics in support of the drug development of IND, NDA, ANDA, and 505(b)2 submission studies. He also has rich professional experience in handling various regulatory inspections such as USFDA, WHO, ANVISA, MHRA, MoH Turkey, French -Affsaps, THAI-FDA GLP, MCC-South Africa, GCC (Gulf Countries Council), Ministry of Health, Kazakhstan and CDSCO
Mr. Sadanandam Eega is the Head - Quality Assurance at Jeevan Scientific Technology Limited. He has around 18 years of experience in Quality Assurance in the domains of Bioavailability and Bioequivalence (BA/BE), Preclinical, clinical trial studies and Pharmacovigilance. He is also a well-versed auditor in compliance with applicable GCP/GLP regulations and drug regulatory affairs.
Mr. Sadanandam in his career has faced over 50+ national and international regulatory inspections like USFDA, UK-MHRA, FRENCH, WHO, ANVISA, NPRA-MALAYSIA, MOH-BELAURUS, SFDA, MCC-SOUTH AFRICA, CDSCO-DCG(I), DMHO, NABL (ISO 15189: 2012) and ISO 9001:2015 (UKAS).
He is associated with JSTL since Jan 2022 and prior to that he worked with Aizant Drug Research, Actimus Bio, NEKTAR Therapeutics and Aurobindo. At JSTL, as a QA Head he is responsible for QMS maintenance, continual improvement of quality systems, automation, managing client audits, regulatory inspections and other QA functions, as well as assuring that the conduct of clinical research studies is in accordance with ICH GCP, OECD GLP and applicable regulations/guidelines and SOPs.