Upcoming Webinar

CLINIMINDS - SINCE 2004 (21+ YEARS NOW)

12,000+ Cliniminds Alumni

Event Name Date Time Venue Registration
New-Age Career Opportunities in Life Sciences Sector ( Drug Regulatory Affairs) 6th July 2025 12:00PM IST Zoom Register

Join us for a free session on "New-Age Career Opportunities in Drug Regulatory Affairs.

India’s pharmaceutical and healthcare sectors are experiencing rapid expansion, creating a growing demand for skilled professionals in drug regulatory affairs (DRA). With strategic government initiatives and increased foreign investment, the drug regulatory landscape is projected to generate a substantial number of job opportunities in the coming years.

Drug and medical device regulatory affairs involve managing the processes required to bring pharmaceutical and medical device products to market and ensuring they comply with all applicable regulations throughout their lifecycle. Regulatory professionals work to ensure that products meet all legal and scientific standards from initial development through to post-market surveillance.

Regulatory affairs encompass a wide range of activities, including preparing and submitting regulatory documents, interfacing with regulatory agencies, ensuring compliance with regulatory requirements, and keeping up-to-date with changes in regulations. This field is vital for ensuring that safe and effective products are available to patients and consumers.

Keynote Speakers

  • Mr. Kamal Shahani - Managing Director

    Program would be inaugurated by Mr. Kamal Shahani, Founder & Managing Director, Tenet Health Edutech Pvt. Ltd. Over 30 years of rich business & consulting experience in the healthcare & life sciences, skill development, had successfully set up and managed several greenfield projects in healthcare, life sciences & clinical research and education sector.

  • Mr. Prakash B - Senior Regulatory Expert

    He is a Masters of Pharmacy in Drug Regulatory Affairs & Pharmaceutics and having 9+years of rich Pharmaceutical experience in the areas of International Regulatory Affairs and post approval changes.  He is expert in planning and submission of Marketing Authorization Application as per CTD, eCTD, ACTD for US, EU, ROW, Singapore Malaysia & Brunei, Thailand Markets format in line with Country requirements.

Who should attend this webinar?

  • Pharmacy Graduates / Postgraduates – B.Pharm, M.Pharm, Pharm.D
  • Life Sciences Graduates / Postgraduates – B.Sc, M.Sc, B.Tech / M.Tech in Biotechnology, etc.
  • Medical Graduates / Postgraduates – BDS, BHMS, BAMS, MBBS
  • Clinical Research Professionals, Pharmacovigilance Professionals, etc.
  • Working Professionals from Lifesciences, Healthcare, and Pharmacy sectors