Clinovo works with life sciences customers to help accelerate Drug Development through our adaptive engagement models. Our customized, fit-for-purpose clinical development support services potentially meet the unique clinical biometrics needs of our customers globally and across multiple therapeutic areas. Clinovo’s customer value is through improved speed to accurate submissions, decrease clinical development cycle times and lower development & operational costs. Clinovo is an ISO certified specialized global service partner for pharmaceutical, biotechnology and medical devices companies delivering excellence on their clinical development value chain. Our fully integrated delivery model connects the right expertise, processes and technologies to bring new therapies to market and improve quality of life for patients globally. Clinovo aims at accelerating clinical development process by supporting across most critical elements of the clinical development value chain. Our services span across the niche functional capabilities like; biostatistics & programming, clinical data management, clinical operations, medical writing, pharmacovigilance, and drug regulatory operations. Clinovo offers world class customer experience through adaptive project governance and flexible business engagement models. For value driven clinical project deliverables Clinovo offers customized approach and can be engaged as your Functional Service Provider (FSP) or Functional Service Outsourcing (FSO) and through remote staffing models. Our passionate consulting experts have extensive industrial experience and are equipped with deep process and technology understanding to enhance your efforts for accelerating clinical development. Our teams have rich experience in successfully establishing and delivering on large multi-year global FSP/FSO engagements. Our Offshore CoE located at Hyderabad, India is a fully compliant centre to cater to our clients across global time zones.