10 Small Submissions
No more than 10 Documents per submission
Health Authorities of different countries have incredibly detailed guidelines for all kinds of categories - pharmaceuticals, medical devices and cosmetics. The ever-evolving HA regulations make it impossible to keep track and adapt at the same pace. The effort of researching, integrating and analyzing the relevant updates in the industry and implementing the time-critical Regulatory requirements is laborious.
Freyr IMPACT, a Regulatory intelligence software, eases out the research and development lifecycle by substantially reducing work and quickening decisions. Freyr IMPACT stands unique with features such as a centralized repository with global access to comprehensive Regulatory and associated intelligence. In addition, it can track, distribute and consume the real-time insights with user workflow of content creation, distribution, tracking and compliance reporting.
in-depth Insight of new product development, new market, and geography
ability to store and archive information and support documents
analysis of Regulatory pathway & hurdles, interpretation of laws, regulation, and guidance
summary of insights with heat maps and customizable dashboard with user-friendly navigation
upcoming regulations related discussions/updates through congress coverage/trade associations
HA alerts and ad-hoc HA queries
comprehensive, global, Regulatory repository with intuitive search algorithm
search can perform in associated reference documents and literature
QC workflow, compliance tracking & insight audit trail
a dashboard displays a complete visual snapshot of the knowledge repository categorized and assorted
Regulatory insights can classify into user-defined dynamic categories built as the information repository grows
web crawlers & automated robots for alerts