Advisory Board

The CliniExperts Advisory Board brings to you best of both worlds – pharmaceutical regulatory insight combined with decades of experience. Our panel of experts will ensure smooth navigation through the Indian regulatory algorithm to accomplish your product launches, registration, and license procurement with their in-depth knowledge, exhaustive network and timely advice.

Dr. Arvinder Singh

Dr. Arvinder Singh, a former member of FICCI National Biotechnology Committee, holds over 25 years of experience in the Biosciences & Invitro clinical diagnostics business operations and strategy. He has spearheaded the management front of some of the leading biosciences firms like Becton Dickinson (BD Biosciences), Boehringer Mannheim India, Perkin Elmer India, Dako Denmark and at Human Diagnostics GmbH to name a few, heading some of them at the national and south east Asia level. He has closely worked with Indian life sciences, Biotech, and Invitro clinical Diagnostics industry and also with India's leading R&D institutes under the governance of CSIR, DBT, DST, ICMR, DRDO, etc.
A Co- Chair of International Membership Services – ISAC, US (2006-08) and a Founding Member of the "The Cytometry Society of India", he has been a Founding Member of the Indo-US Flow Cytometry Workshops which are conducted every year in leading Indian institutions in collaboration with American universities since 2001. Dr. Singh brings to CliniExperts this rich business operations and advisory experience spanning various aspects of the biosciences and healthcare fields.

Dr. Girdhari Lal Singal

Dr. Girdharilal Singal stands tall with his immense experience in the pharmaceutical vigilance industry. As a stalwart of Food and Drugs Control Administration of Haryana State HQ for over 10 years he has over 13 publications in national and international journals of repute.
With his commitment and full dedication, Dr. Singal became Joint Commissioner and State Drugs Controller for Haryana from 2012-14. He represented the country as a temporary advisor in 49th WHO-Expert Committee on Specifications for Pharmaceutical Preparation in Geneva (Switzerland) from 13-17,Oct.2014. His vast experience in the pharmacovigilance and medicolegal field have seen him  participate in many international conferences and present insightful papers at national and international forums.
He has been part of WHO/HAI workshops and conferences too. Dr. Singal's knowledge and expertise is an asset to the CliniExperts Advisory Board. Dr. Singal was also associated with Ranbaxy Ltd as a Research Scientist for Product Development in the initial years before pledging his efforts for the Haryana State administration for the next decades to come.

Dr. Kulwant Saini

A professional par excellence with a strong academic background in pharmaceutical sciences, Dr. Kulwant Saini boasts of more than three and half decades of experience in the pharmaceutical and medical device industry. CliniExperts is proud to have Dr. Saini on the advisory board.
With a career spanning 22 years of meteoric rise in Johnson and Johnson alone, Dr. Saini has deftly handled various aspects of pharmaceuticals and Medical Technology, ranging from regulatory affairs, quality management system, research, clinical affairs, drug development to technology and product assessment. He holds comprehensive industrial experience as regards medical device design control, risk management, manufacture, and QMS to life cycle management.
His on-site experience is fortified by skillset in due diligence, licensing, acquisitions, deals, and alliance management on the business management front.
He has well rounded knowledge of ISO, GCP, GLP, US FDA, EMEA, MDR/IVDR and other regulations on the regulatory front.
His expertise in technical writing, QMS assessments of organizations/Certifying bodies and immense experience have made him an indirect shaper of the Medical Device regulations in India.

Mr. Rakesh Sharma

Mr. Rakesh Sharma is renowned personality in the field of medical devices and related regulatory affairs. He brings to CliniExperts, his wide-ranging experience of over 30 years. Mr. Sharma has helped several Fortune 500companies such as Dickinson India, Gillette India, and many more, to establish their regulatory parameters. He possesses end-to-end consultancy expertise on all critical touch points - Regulatory Affairs, Government Affairs, Supply
Chain Management, Public Policy Imports /Exports, Logistics, Procurement etc. In particular, Mr. Sharma is a pioneer of medical devices' regulatory affairs. Mr. Sharma's global experience spans helping international companies in their India entry, and providing consultancy to Indian companies in deepening their global footprint. He is well versed with the legal and regulatory affairs of all major geographies. Mr. Sharma is an important resource of consultancy for the Indian Government. He is a member of many important institutions of national and global repute, such as FICCI, CII, ADMA, American Chamber of Commerce, and others.

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