Join us on | Download Brochure  |  Latest Insights

Certificates, Licenses and Membership

About Us

We aspire to render clinical support services to Pharmaceutical, Biotechnology and Contract Research Organizations for the last 11 years by emphasizing the utilization of modern technologies to ensure utmost quality and assist them to achieve their goals.

What We Do

Ancillarie offers Biostatistics, CDISC Implementation and Mapping, Clinical Data Management, Clinical Operation, Medical Writing, Pharmacovigilance, Statistical Programming, Quality Management and Resourcing Services.

We have in place various service models and we also work with our client to develop different service models as their need :

Our Services

Our Statistics

10 +
YEARS OF SERVICE
20 +
GLOBAL STRATEGIC PARTNERS
25 +
TOTAL PROJECTS COMPLETED
12800 +
TOTAL SUBJECTS ENROLLED
538980 +
TOTAL CRF PAGES PROCESSED

Why Ancillarie

We are ISO 9001:2015 certified global clinical support service company with a decade of experience committed to provide quality driven services. We continuously make improvements to the services we provide to our clients.

We prioritize client expectations
We strive to deliver quality service output
We aspire to implement ‘Innovation in Business’.
We stand by our values.
We prioritize client expectations
We strive to deliver quality service output
We aspire to implement ‘Innovation in Business’.
We stand by our values.

Latest Insights

2023 -- Ancillarie has sponsored the event . . .
2022 -- Ancillarie successfully celebrated 10 years. . .
2020-2021 --Ancillarie Successfully passed audit . . .
2018-2019 -- CDA signed with US based. . .
2016-2017-- CDA Signed with Russian based. . .
2012-2015 -- Ancillarie successfully completed Data. . .

Career

If you are ready to take challenges, turn opportunities into success and dream to step the ladder of success then Join Us

Canada

Ancillarie,
500-1450 Meyerside Drive, Mississauga, ON L5T 2N5, Canada.

India

Ancillarie LLP,
A-215 – Kanakia Wall Street, Andheri – Kurla Rd, Chakala, Hanuman Nagar, Andheri-East, Mumbai-400 093, Maharashtra. India

Join us on

Copyright © 2023. Ancillaire | Website Designed by Aarav Infotech

Insights 2023

Insights 2022

Insights 2020-2021

Insights 2018-2019

Insights 2016-2017

Insights 2012-2015

Write us

RFP form

Thank You!

Your submission has been sent.

Shantanu Bagwe

Shantanu Bagwe

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.

Ramona Petrita

Ramona Petrita

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.

1668134826968

Kim McDonald-Taylor

MSc, CRPC
  • Kim McDonald-Taylor, MSc, CRPC is a Clinical Research Professional with more than 34 years of experience including her 12-year tenure with Endpoint Research holding positions such as VP Operations and Managing Director of Canada. She has worked in virtually every therapeutic area
  • Kim is providing technical guidance to Ancillarie in Canadian Clinical Operations . She operates a clinical consultancy, McDonald-Taylor Consulting, where her passion for her clients’ projects results in exceeded expectations for her training, project management, SOP creation, medical writing, teaching, meeting facilitation and strategic planning.
  • Kim received the Excellence in Clinical Research award in 2018 at the Canada Talks Pharma conference. Kim has volunteered with the Clinical Research Association of Canada (CRAC) ™ for the past 20 years.
  • Kim earned her MSc in toxicology from the Ontario Veterinary College at the University of Guelph. She has presented and co-chaired sessions at DIA, DIA Canada, ACRP and other meetings over the past 20 years
Amiit Keshav Naik

Amiit Keshav Naik

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.

SEND YOUR CV

Blank Form (#3)

Medrio

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

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

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

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

Statistical Consulting

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

Phase I and Bioequivalence

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

Clinical Operations

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

Dr. Suresh K Bowalekar

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:

  • Chartered Statistician (C.Stat.) – the highest credentials in statistics in 1993, jointly by the Royal Statistical Society, London and Institute of Statisticians, U.K.
  • Chartered Statistician (C.Sci.) by The Science Council, UK, 2009.
  • Recipient of “Indira Gandhi Sadbhavana Award” for 2005.
  • His name is included in 2007-2008 edition of International WHO’S – WHO directory of professional.

At the initial span of his career, he spent couple of years in teaching. Post that he spent almost;

  • 10 years in banking and economic statistics with Econometric Department of the prime bank of India – Reserve Bank of India.
  • 11 years in Pharma MNC Searle India Ltd.
  • 11 years in the top management team of Wockhardt Ltd.
  • 3 years in Quintiles – a Global CRO, he established DM & Biostatistics Unit in India.
  • Retired as Managing Director, of PharmaNet/i3, India after serving it for almost a decade.

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;

  • General Secretary of ISCR (Indian Society for Clinical Research)
  • Appointed Member of BoT (Board of Trustees) Of SCDM
  • Member of Governing Council of IASCT (Indian Association for Statistics in Clinical Trials)

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:

  • Guidelines on Bioequivalence studies for immediate release
  • Guidelines on Bioequivalence studies for modified release drugs
  • Good Clinical Trial Regulations in India (GCTRI).

Dr. Jack Green

 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.