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. 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.


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