Syncorp Health Pharmaceutical Research Services (SYN-PHARMA) team has been ensuring customers in the Pharmaceutical & Biotechnology industries to achieve their clinical research goals for over 10 years. As experts in the planning and delivery of clinical research, we understand the importance of time, cost and quality through the defined metrics and SLAs.

Syncorp Health Medical Device Research Services Organization (SYN-MRO) team has expertise and understands medical device and diagnostics regulations; Our Medical device team has been through the regulatory process for clinical trial, Clinical Validation and product approval in the Central Drugs Standard Control Organization(CDSCO) India, South Korea MFDS, USA and EU many times.

Syncorp Health Nutraceutical Research Services (SYN-NUTRA) team has expertise and understands nutraceutical regulations; Our team has been through the regulatory process for clinical trial, Clinical Validation and product approval in the Food Safety and Standards Authority of India (FSSAI), South Korea MFDS, USA and EU many times.

Syncorp Health Ayurveda Research Services (SYN-AYUR) team has expertise and understands the Ministry of Ayurveda, Yoga & Naturopathy, Unani, Siddha and Homoeopathy(AYUSH) regulations; Our team has been through the regulatory process for clinical trial, Clinical Validation and product approval in the AYUSH, India South Korea MFDS, USA and EU many times.

Syncorp Health Biometrics team has experience in handling Pager and EDC studies in a many number of therapeutic areas. Team has experience in, the Group has implemented CDISC standards and all processes are compliant with ICH guidelines.

Syncorp Health Regulatory Services (SYN-REG) team has significant global experience in drug and device development and establishing regulatory strategies. And we provide the supports in expedited programs, including Fast Track submission and approval with regulatory bodies like DCGI, Korea-MFDS, AYUSH and FSSAI.

Syncorp Health Safety services (SYN-PVG) provides drug safety services to small, mid and large sized pharmaceutical, biotechnology & devices companies. our dedicated team consists of Pharmacovigilance associates and Medical Monitors (Physician) are highly qualified and skilled experts who are committed to helping our customers to meet the challenging demand of producing detailed and accurate safety reports within the regulatory timelines.

Syncorp Health understands the Site Management is a critical part of a trial any success. As per the site Management team performs these key tasks (but not limited to these listed)

Syncorp Health provides an assistance to customers and Sites by Smoothing the Clinical Trial Management Process

We work to bring solutions to following related to Investigators, sites and Sponsors

Syncorp Health conducts clinical research studies & generate the Clinical Quality Documents, GCP Documents, safety and efficacy data of their investigational products and other trials related data.Syncorp supports with appropriate tools that supports the sponsor organizational processes, under which clinical studies Document Management strategies can be planned, performed, monitored, recorded & archived.

Syncorp Health team with deep domain knowledge assists the customers in solving business challenges and provides consultation by offering following consulting services:

Syncorp Health Educational efforts aimed at the public and health care providers, to raise awareness of the concept of clinical research and the important role it plays in improving health and quality of life.