Regulatory Affairs Services

Embrace limitless growth possibilities with Freyr's Regulatory Affairs services. Navigate Regulatory landscapes effortlessly and amplify your product's value to dominate in the life sciences, pharma, and consumer realms. Let's elevate your product’s market impact.

  • ZERO
    Refusal-to-File from Any Agency, due to CMC Technical Errors
  • 260

    +

    Regulatory Affairs Experts
  • 18000

    +

    Projects
  • 100

    +

    Countries
  • 8
    Forbes Global Top 10 Drug and Biotech Companies
  • 65

    +

    Mid and Small Bio-Tech / Bio-Similar Companies
  • 190

    +

    Generics and API Manufacturers/Sponsors
  • 400

    +

    Products
  • 250

    +

    Formulations

Regulatory Affairs Services - Overview

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 (HA). Ensuring compliance throughout the process is a mandatory requirement. To avoid overlooking procedures across the product life cycle, organizations deploy proven experts for Regulatory Affairs Services and consulting. The expert team acts as a crucial link between the organization and global HAs, 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.

As a specialized global Regulatory service consulting partner, Freyr acts as a bridge between organizations and key Regulatory authorities like the US FDA, Health Canada, and the European Medicines Agency. Freyr is a leading Regulatory Affairs Services company and has been a pioneer in providing strategic Regulatory support services globally. 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 biological products and medical devices companies to understand and efficiently manage the demanding complexity of the diverse Regulatory requirements to successfully launch their products in new markets and maximize their market value.

Regulatory Affairs Services

  • Regulatory submission forecast and planning
  • Submission document management and tracking
  • Regulatory content management
  • Change control management
  • Tracking label changes
  • Integrating Regulatory information
  • Regulatory Intelligence
  • Seasoned Regulatory experts upholding Regulatory compliance
  • Enhanced documentation support via in-house developed tools
  • Data-driven insights with AI-integrated tools
  • Accurate labeling implementation using industry benchmarking software
  • Informed Regulatory decision capabilities in line with global regulations
Regulatory-Affairs-Services-advantages

Success Stories

Freyr Enabled a German Multinational Pharmaceutical and Life Sciences Company to Successfully Execute an OTC Market Switch Application in Brazil
Regulatory Affairs

Freyr Enabled a German Multinational Pharmaceutical and Life Sciences Company to Successfully Execute an OTC Market Switch Application in Brazil

Celebrating Customers Success

 

Medicinal Products

Regulatory Affairs

India

Thank you for the timely support over the weekend, which allowed us to resubmit quickly after being notified. This continuously demonstrates Freyr's commitment towards our company’s milestones.

Director - Global Regulatory Affairs – Operations

India-based, Global Top Generic Pharma Company