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A Trusted, Experienced Partner for Regulatory Submissions
The number of clinical documents required by regulatory agencies has increased dramatically with new drug and device safety guidelines. Syntel can help you meet these dynamic regulatory requirements with a suite of submission publishing services for all phases of the pharmaceutical and medical device development process, including consulting, compilation and submission lifecycle management, as well as regulatory IT services.
Our publishing team is made up of doctors, life sciences experts, and technology specialists ready to translate your complex data and results into formatted, regulatory-compliant documents — enabling you to meet strict timelines and secure approvals for your products across multiple global markets.