Our Team
Leadership Team
Our team is the cornerstone of our success, an exceptional group of skilled professionals driven by a shared passion for excellence. With a seamless blend of expertise, innovation, and dedication, we are committed to delivering unparalleled solutions for the pharmaceutical and medical device industries.
We combine deep industry insights with forward-thinking strategies to help you navigate complex regulatory landscapes, ensure compliance, and enhance operational efficiency. With a focus on continuous improvement and client-centered service.

Dr. Mahesh Kumar
Director and Co-Founder
Dr. Mahesh Kumar a pharmaceutical quality assurance professional
with diverse and comprehensive global experience in setting up
quality systems for cGMP, GCP, GLP, GCLP,CSV activities of drug
development for IND to NDA/BLA submissions and ANDA
submissions.
• 23+ years with Nektar, Aizant, Pliva, Torrent, Sun Pharma.
• Management and auditing of CROs and CMOs globally for GCP, GLP, cGMP
• 50+ External audits, 300+ Sponsor audits.
• 100+ Internal audits.
• Hosted 50+ regulatory inspections - USFDA, EMA, ANVISA, WHO, MoH Turkey, DCG(I), OECD GLP, ISO 17025, ISO 27001, ISO 15189.
• 23+ years with Nektar, Aizant, Pliva, Torrent, Sun Pharma.
• Management and auditing of CROs and CMOs globally for GCP, GLP, cGMP
• 50+ External audits, 300+ Sponsor audits.
• 100+ Internal audits.
• Hosted 50+ regulatory inspections - USFDA, EMA, ANVISA, WHO, MoH Turkey, DCG(I), OECD GLP, ISO 17025, ISO 27001, ISO 15189.
- Email:info@clintask.com

Prabhat Kumar
Director and Co-Founder
25+ years of experience in the entire lifecycle of drug & Medical
device development. Contributed to many drugs to reach
market/patients including the first Covid vaccine and drug, and firstof-
class AI/ML-enabled PV case processing and medical narrative
writing system.
• 18+ years with Accenture, PAREXEL, TEVA
• Hosted 80 + Regulatory inspections across Asia, Europe, Australia, and middle east.
• Conducted 250 + GXP audits, Mock Inspections (Investigator site, Clinical functions, PV, CDM, Programming, computer system, Medical, Regulatory, Medical Imaging, Clinical logistics, drug depot, Manufacturing site, IT vendors.
• 18+ years with Accenture, PAREXEL, TEVA
• Hosted 80 + Regulatory inspections across Asia, Europe, Australia, and middle east.
• Conducted 250 + GXP audits, Mock Inspections (Investigator site, Clinical functions, PV, CDM, Programming, computer system, Medical, Regulatory, Medical Imaging, Clinical logistics, drug depot, Manufacturing site, IT vendors.
- Email:info@clintask.com