Half a century of experience as an entrepreneur renders Mr. Singh with a business acumen that’s second to none. He set out a clear vision from the beginning and through his enthusiasm and sound decision making ADI CRO has prospered. Despite tasting unparalleled success the man is an epitome of humility and has his humanitarian spirit still intact.
The President and CEO of ADI CRO is a man well known for his capability to understand and analyze a problem and come up with a solution. A thought leader and entrepreneur, Mr. Matharu is well known for being the ‘Solution Person’ in the industry. His 20 years of experience and expertise in all matters pharmaceutical, healthcare, IT, and medical animation has seen Mr. Matharu build various companies from start-up to market leader corporate level. This reputation often sees him quoted in various publications around the world.
Mr. Matharu has mentored many who still work for ADI CRO and the wider group. His reputation and expertise is far reaching.
Ken Robinson, the founder of Robinson RegDocs is a veteran in the world of pharmaceutical/medical documentation. With a rich journey of twenty committed years, he holds to his credit the establishment and direction of the supervisory writing groups at Sterling Winthrop, Sanofi, DuPont Pharmaceuticals, and Bristol-Myers Squibb. A thorough wise of ways, Ken has best utilized his skills in international settings, helping many companies formulate time saving plans for documentation and submission.
Ms. Vohra has been a key contributor to all strategic recommendations and driving growth in global operations since the inception of the firm. All the while, each of her strategy and decision has focused on client satisfaction and developing new business opportunities for existing and potential clients. Her roles so far have been those of HR Manager, Business Development Manager and Corporate Communication Manager, by virtue of which she now possesses keen organizational instincts that do justice to her role as the director of ADI CRO.
Neerja has been with us since 2007 and in that time has successfully delivered projects which involved complex trials and clinical trial data assignments and developed bespoke clinical trials solutions for a diverse array of clients. With five years of experience working in the Central Nervous System (CNS) therapeutic area, she oversees projects which fall under this umbrella.
Neerja holds a Masters in Biotech, and ensures that the medical writing teams, medical animation teams and common technical document authors meet their deadlines.