	Clinical trials • IND Preparation and Submissions • Phase 1 & BE testing • Phase 2-4 • NDA Regulatory affairs consulting & report submission • Data management • Clinical sample testing		Clinical trials capability Maya Clinicals extensive network of hospitals across India draw upon a vast patient pool and can accelerate patient recruitment across a broad range of therapeutic areas. Maya Clinicals has comprehensive customer solutions to address the entire clinical trials process from initial IND submission through the clinical trial to final report submission to the FDA. Pre-Qualified Facilities Our pre-qualified doctors, hospitals and CRAs are fully trained and compliant in GCP and have experience in trials submitted to the USFDA for the North American market. Clinical Samples can be tested locally at GLP compliant laboratories in India or shipped to Central laboratories using a streamlined, accelerated process.



	Ethical Standards Maya Clinicals’ network of doctors and principal investigators follow the highest ethical standards when conducting clinical trials in India. All of the hospitals conducting trials in Maya Clinical’s network are overseen by independent review boards.				Maya Clinicals has extensive regulatory affairs expertise across US, European and Indian regulatory agencies.