VIMTA has rich experience, vast knowledge, advanced technologies and IT powered processes to conduct studies. With strong know how and international regulatory experience VIMTA is the right partner for conducting clinical research studies in India.
VIMTA’s success is driven by its commitment to support customers win through thorough understanding of the critical importance of time, effective program management and GCP & GLP compliance. VIMTA has conducted more than 200 BA / BE studies for submissions to USFDA, MHRA, DCGI and other regulatory bodies across the globe. VIMTA has a database of over 26000 healthy volunteers and a biometric based screening system in place.