Regulatory IT Services

Digital Services


Atos|Syntel provides global regulatory IT services and lifecycle management for all phases of the pharmaceutical and medical device development process.



  • Clinical trial applications
  • Medical writing and dossier preparation
  • Change control management
  • Compliance and business risk consulting
  • Quality management and quality control
  • Regulatory and compliance management
  • Post-approval lifecycle management
  • Submission and data management


The Atos|Syntel Advantage

  • Expert team to manage adherence to regulatory requirements for pharmaceutical and medical product development programs
  • Consolidated framework for end-to-end pharmaceutical regulatory affairs, including dossier preparation, submission review and filing
  • Agile methodology to quickly implement revised plans as regulatory requirements change

Close Form

Request Information

Looking for a solution to meet your business needs? Please fill-in all the details in the following form and we will get in touch with you shortly.

Add numeric values
By submitting this form, I consent to my personal data being used as described in the Atos|Syntel Privacy Policy.