Newsletter

Let’s recognize Jaldip Vyas, a key member of our team, whose expertise in Quality Assurance (QA) and compliance has played a vital role in maintaining the highest industry standards. Jaldip holds a master’s degree Pharmacology. With over 15 years of leadership experience in QA for clinical trials and pharmacovigilance, Jaldip has a proven track record of driving quality initiatives and ensuring regulatory excellence.    

Before joining Celito, Jaldip led the Medical QA function at a pharmaceutical company, overseeing compliance and audit processes. As a CQI and IRCA-certified ISO 9001:2015 Lead Auditor, he specializes in conducting GCP audits across investigator sites, systems, processes, and vendors in regions including Europe, the Americas, MENA, and APAC. His meticulous approach helps safeguard the integrity of clinical trials and patient safety. 

Jaldip’s expertise extends beyond audits—he contributed to the development of ICH GCP R3 as a public consultant, engaging in global regulatory discussions to shape industry best practices. He is also a recognized speaker and panelist at international conferences, sharing insights on quality and compliance in clinical research. 

Outside of work, Jaldip enjoys traveling, spending time with family, connecting with nature, and singing. His dedication to excellence and continuous improvement makes him an invaluable asset to our team. We’re proud to have him on board!