We are into clinical trials for a wide arena of solutions ranging from paediatric, adult inpatient as well as outpatient studies. We have affected more than 150 plus successful submissions across USFDA, MHRA, EU, Korea and other acknowledged institutions. We undertake the entire clinical development process for our clients. Our expertise can be explored in the different genres- • Protocol Development • Medical and regulatory consultations • Pre-clinical testing • Bioequivalence/Bio-availability Studies • Phase I-IV clinical trials • Clinical trial monitoring • Project management • Central Laboratory services • IRB and IEC submissions/Approvals • ICH-GCP investigator training • Site management and auditing • Pharmacovigilance • Data management • Statistical analysis • Medical writing / Registration dossiers • Medical and pharmaceutical text translation • Immunogenicity Markers • Bio Markers