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We have been dedicated to patient recruitment for an extensive period, collaborating with leading pharmaceutical and biotech companies on numerous successful campaigns across diverse therapeutic areas. Throughout this journey, we have made a significant impact on patients worldwide.
We are delighted to announce our successful clearance of a surprise inspection by the USFDA. This achievement marks our approval as a USFDA-recognized on-ground workforce in the field of clinical research.
At Neomed, the realms of clinical and commercial aspects coexist under one roof. We consistently foster an environment where real-world knowledge and insights are shared seamlessly, resulting in more effective, intelligent, and expedited outcomes.
Our patient recruitment Experienced Execution service is synonymous with precision, excellence, and transformative impact. With a rich legacy of successful collaborations, we navigate the complexities of clinical trials with adept coordination, ensuring protocol adherence and successful enrollment.
We understand the pivotal role of Essential Partnerships in patient recruitment success. Collaborating seamlessly with pharmaceutical and biotech leaders, we forge strategic alliances that drive impactful campaigns across diverse therapeutic areas. Our commitment to precision and ethical considerations ensures trials are conducted with integrity.
We redefine patient recruitment with a commitment to precision and excellence. Leveraging extensive experience, we navigate the intricacies of clinical trials seamlessly. Cleared by a rigorous USFDA surprise inspection, we stand as a symbol of trust and reliability.
Dedication is the heartbeat of our patient recruitment ethos. With unwavering commitment, we embark on every clinical trial journey, ensuring precision, ethical integrity, and strategic execution. Cleared by a stringent USFDA surprise inspection, our dedication to quality is unwavering.
Founder & CEO
Trial Expert for Phase I to IV bioequivalence studies
A medical expert with experience of more than 15 years in clinical trials with an experience in facing various regulatory audits as well as expertise in medical writing and study designs.
Co Founder & HeadOperations
Trial Expert for Phase I to IV, bioequivalence studies and studies on special populations
She is clinical trial expert with more than 20 years of experience in subjects or patients recruitment , study conduct , regulatory inspection handling, report writing. she is one of few experts in india capable of conducting studies in special population.
