AXIS Clinicals Limited is one of the most experienced and fastest growing Clinical Research Organization incorporated in September 2004.
Our state-of-the-art facilities houses 500+ dedicated full-time professionals to ensure the quick turn around time with high quality. Our facilities are accredited by DCGI (Drugs Controller General – India), NABL (National Accreditation Board for Testing and Calibration Laboratories - ISO 15189:2003) and inspected by US-FDA, UK-MHRA, Brazil-ANVISA and France –AFSSAPS and conforms to ICH and CDSCO-GCP & GLP Guidelines.
Within short span, we have achieved the milestone of completing 1200+ clinical studies, 300+ ANDA study completions and 50+ product approvals from various regulatory agencies.
Ten plus (10+) regulatory audits from global competent authorities is testament to our professionalism and dedication to quality studies.
Our Phase 2 – 4 capabilities are growing along with an extended portfolio of Site Management, Medical Writing, and Data Management.
Specialties
Bioequivalence / Bioavailability studies, Clinical Trials, Special / Patient Population (PK/PD) studies, Clinical Data Management
