At SYNCORP, we bring on table for our customers the latest technology that simplifies drug development process. 

Clinical Trial Project Management team is experienced in the administration and regulatory aspect of clinical research and drug development with an extensive network of contacts throughout the pharmacy industry in India and internationally.

Data management team is experienced in all aspects of data management which includes design and maintenance of the clinical research database, writing data management plans, design and implementation of quality control and quality assurance process and data validation.

Clinical data management process is carried out on the latest technology. It is fully complaint and completely validated tool.

Our statistical functional team is well equipped with software used to perform biostatistical analysis of data. The software is validated and compliant to regulatory requirement which ensures the client of receiving descriptive statistical reports.

On every medical writing demand of the client, SYNCORP delivers the work with quality and timeline plan, to ensure project stays on track. SYNCORP medical writing services include clinical and regulatory writing as well as scientific communication, education materials and medical writing consultancy. Our medical writing team work closely with our project management, biostatistical and data management team to deliver accurate and timely document to the client with ethical and scientific standards. Our team also have the access to latest plagiarism checkers

SYNCORP carefully designs and plans internal audits to evaluate whether current trial project management, data management, medical writing and statistical services adhere to the SOPs, regulatory requirements, and international standards.