With more than 12 years of experience, Ancillarie can provide
expert support that will help you to succeed in your clinical studies.
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CA, Chief Financial Officer
Shantanu Bagwe is a Chartered Accountant (India) and MBA in Finance from UBI, Belgium with an experience of more than 10 years in Finance.
He has diversified Experience in Indirect Taxes and Foreign Trade Policy of more than a Decade. Eminent Speaker at Various Events of ICAI (India), Trade Associations, Corporate Channels, Leading National TV Channels, etc.
Contributor of Publications in ICAI, Newspapers, etc and Group Member of Taxation Audits Quality Review Board (Indirect Taxes) of ICAI.
B.Pharm, Chief Scientific Officer
Pharm. Ramona Petrita [F] ( Bachelor’s Degree in Pharmacy) is Clinical Research Professional with more than 15 years’ experience in Pharmaceutical Research Industry.
Ramona is currently leading the scientific and clinical operations at Ancillarie in Europe. She has skills in project management, strategic thinking and decision-making. She brings to the team is experience with developing strategic partnerships. This includes important networks with the pharmaceutical industry and medical organizations/societies, as well as with medical experts and healthcare authorities.
As Scientific Officer Ramona will provides professional leadership and expert clinical advice across the Organization by overseeing the scientific functions of companies and the design of clinical studies and associated research protocols. Moreover, Ramona is involved in several other roles: writing and reviewing scientific documents, coordinating research activities, designing and implementing objectives, managing performance, and reviewing and approving the standard operating procedures.
She has worked as Clinical Project Manager in an East European Contract Research Organization where she successfully coordinated more than 10 multinational clinical studies.
Founder and Chief Executive Officer
Amiit Keshav Naik (Graduate in Statistics, Post Graduate in Mathematics and Statistics, Executive Certificate in Entrepreneurship from Indian Institute of Management and Certified Graphologist ) is a Clinical Research Professional and his experience includes setting up Data Management & Biostatistics departments with managing team size of 250 professionals for various multinational CROs.
With more than 22 years of professional experience including 17 years of Professional Experience for top CROs; He has proven his strengths in Project Management which comprise of monitoring processes like Data Management, IVRS, SAS programming processes and External Vendors for more than 200 studies across different therapeutic areas.
He has provided his expertise to the Business Development team to develop proposals for Bid Defence Meetings. His strong leadership and communication skills facilitates diverse cross-functional teams to deliver positive results.
He has built reputation for efficiently meeting challenges in rapidly changing environments while consistently delivering excellence.
Amiit also has supported academia as visiting faculty for Data Management subject at a Pharmacy College. He has also worked as paper setter and examiner for Biostatistics and Data Management subjects for M.Sc. Pharmaceutical Medicine.
He has built reputation for efficiently meeting challenges in rapidly changing environments while consistently delivering excellence.
Amiit also has supported academia as visiting faculty for Data Management subject at a Pharmacy College. He has also worked as paper setter and examiner for Biostatistics and Data Management subjects for M.Sc. Pharmaceutical Medicine.
Medrio offers an eClinical Software as a Service (SaaS) application with an online Electronic Data Capture (EDC) system that doesn’t require any programming.
With 1300+ studies, 500+ customers, and a 98% satisfaction rate, Medrio provides simple, fast, and affordable tools for clinical trials, including a specialized product for Phase I.
For more details, please visit: www.medrio.com
Castor is an ISO 9001 and ISO 27001 certified, 21 CFR Part 11 validated, GDPR & HIPAA Compliant Electronic Data Capture (EDC) system.
Castor’s built-in EDC system makes it easier to deploy studies faster with following features :
For more details, please visit: www.castoredc.com
Clinion is a 21 CFR Part 11 validated Electronic Data Capture (EDC)TM and Clinical Data Management (CDM) system.
Clinion is focused on reducing the new product time-to-market for Pharmaceutical, Biotech, and Medical Device Organizations by providing a highly configurable and user-friendly Clinical Trials Solution. Clinion is headquartered in Hyderabad, India.
For more details please visit: www.clinion.com
Clinvigilant is an ICH-GCP, GDPR & 21 CFR Part 11 compliant complete configurable Electronic Data Capture (EDC) system. With in-depth knowledge in wide range of industries and expertise they provide easier, faster tools for clinical trials. Clinvigilant has been audited by EMEA, MHRA, USFDA, DCGI authorities till date.
For more details visit: www.clinvigilant.com
Our partnering company based in Germany gives us an edge to connect more effectively to our clients based in Europe.
With help of our partners we provide Statistical Analysis, Consulting, programming and Writing services for our clients based in Europe and rest of world.
For more details please emails us on: contact@ancillarie.com
Our partner is a state of the art hospital certified Medical Centre based in Montreal, Canada. The facility was recently accredited with exemplary standing by Accreditation Canada.
For more details please email us on: contact@ancillarie.com
Our partnering companies based in Buenos Aires- argentina, North Carolina-United States of America are oriented to provide advice, assessment, support and recommendations to pharmaceutical, biotechnology, Medical Device industries and Contract Research Organizations as well as other companies that actively work in different stages of Clinical Trial Development.
For more details please email us on: contact@ancillarie.com
Ph.D., C.Stat.(UK), C.Sci.(UK)
Dr. Suresh K Bowalekar has more than 35 years of experience in the field of Clinical Research and Biostatistics. He retired as the Managing Director of PharmaNet, India in August, 2012.
His able leadership was responsible for systematic growth of PharmaNet at 2 locations in India – Bangalore and Mumbai, within a span of initial 3 years since its inception in 2003.
Dr. Bowalekar, the Fellow of Royal Statistical Society (FSS), London was honoured by various esteemed institutions as follows:
At the initial span of his career, he spent couple of years in teaching. Post that he spent almost;
His two books – “Basic Statistics for Chemist” and “Handbook on Operations Research” are due for publications. He has about 90 research papers and more than 100 presentations to his credit. He has been contributing to the success of CRO industries and participating in continuous progress in scientific thought process by serving following associations in various capacities like;
He is a guide for Ph. D. Students of Yashwantrao Chavan Maharashtra Open University (YCMOU) Nasik, Maharashtra, India. He has served as the member of various committees set up by the Drugs Controller General of India to prepare:
Ph.D.
Dr. Jack Green has held senior-level positions for more than 30 years in both Pharmaceutical as well as Contract Research Industries.
He was one of the founder member of PharmaNet, as Senior Vice President of Biostatistics and Data Management.
He was also associated with Covance as Senior Vice President of Biostatistics and Data Management, at Adria Laboratories as Director of Biostatistics and at Merrell-National Labs as Senior Biostatistician.
Dr. Jack Green has extensive experience in setting up and managing global operations in Biostatistics, Statistical Programming, Data Management, IT strategies and Interactive Technologies.
