Regulatory Intelligence in Pharmacovigilance

NG- Freyr empowers pharmaceutical endeavours by staying abreast with timely and relevant regulatory updates with its dynamic regulatory safety intelligence services. Our cloud-based regulatory intelligence software- IMPACT, offers global insights coupled with region-specific guidance and latest regulatory updates from Health Authorities enabling seamless compliance and strategic decision-making in drug development and drug safety,

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Regulatory Intelligence in Pharmacovigilance - Overview

The Life Sciences industry is governed by regulations, which are continuously evolving to help industry players deliver the best. However, keeping up with the changes in the Regulatory intelligence in the pharmacovigilance landscape can be challenging. To help pharmaceutical organizations in the same way, Freyr provides Pharmacovigilance consulting services.

Comprehensive Approach to Regulatory Intelligence in Pharmacovigilance

Freyr’s approach to Pharmacovigilance consulting services is as follows:

  • Primary research that covers data across country updates, Regulatory updates, congress coverage, trade association coverage, authority & ministry coverage, key opinion leaders, and influencers.
  • Secondary research containing data about country/product, Regulatory landscape, clinical updates, PV intelligence, news, and newsletters.

Freyr offers comprehensive Pharmacovigilance consulting services that can help every life sciences organization create internal Regulatory intelligence Pharmacovigilance processes, thereby complying with HA policies and laws.

Freyr provides Pharmacovigilance consulting services and offers a cloud-based Regulatory intelligence software for a complete spectrum of information that spans various industries, products, and regulation categories.

Regulatory Intelligence in Pharmacovigilance - Expertise

  • Cloud-based Pharmacovigilance Regulatory intelligence software that provides comprehensive, global intelligence.
  • Pharmacovigilance consulting services on regulations for individual countries.
  • Region-wise product-specific (drugs, device, or biologics) guidance and Pharmacovigilance consultancy.
  • Country-specific regional ICSR and aggregate reporting timelines and requirements.
  • Local representation (QPPV, NPPV, etc.) and post-marketing authorization information.

Stay ahead of regulatory changes and trends with our safety regulatory intelligence services