Regulatory Affairs Services

Regulatory Affairs services play a vital role in ensuring the successful development and commercialization of drugs as they navigate the complex and ever-changing landscape of global health authorities. Ensuring compliance throughout the process is a mandatory requirement. To overlook the procedures across the product life cycle, organizations deploy proven experts for Regulatory Affairs consulting. The expert team, in fact, acts as a crucial link between the organization and global Health Authorities, tracking all the key regulations related to the product and prerequisites for its launch. In the current situation, not many organizations have the privilege of having these teams in-house, given their dedicated focus and approach toward innovation and drug safety.

At times, as a specialized global Regulatory Affairs Consulting partner, Freyr acts as a bridge between organizations and key regulators like the US FDA, Health Canada, and the European Health Authorities. Freyr is a leading Regulatory Affairs services company and has been a pioneer in providing strategic multidisciplinary Regulatory Affairs consulting services worldwide. Freyr provides comprehensive Regulatory Affairs services across the spectrum of product development, registration, and commercialization.

Freyr’s global Regulatory Affairs services consultants enable Life Sciences, Consumer, Pharma and Bio-Med companies to understand and efficiently manage the demanding complexity of the diverse Regulatory requirements in order to successfully launch their products in new markets and maximize their market value.


Freyr Expertise

  • Submission Forecast and Planning
  • Submission Document Management and Tracking
  • Regulatory Content Management
  • Change Control Management
  • Label Change Tracking
  • Integrated Regulatory Information
  • Regulatory Intelligence
  • Reporting and Analytics

Know More

About Freyr’s Global End-to-End Regulatory Affairs Capabilities