Redica Systems and Veeva RIM Integration for Regulatory Intelligence

Traditional document-centric, multi-system, and manual knowledge management systems lead to inefficiencies and information loss in regulatory intelligence. This approach results in several challenges:

• Decentralized monitoring of regulatory signals causes conflicting information and redundant efforts
• Inefficient evaluation of signals by global team members, with manual forms and processes, takes time away from high-ROI activities
• Current technology is not designed for specific scope, product, or geography monitoring, leading to missed critical signals or an overabundance of signals
• Non-standardized and open loop processes for triage and impact assessments result in siloed knowledge

Redica Systems provides extensive coverage across multiple countries and product categories including Human Drugs, Biologics, Medical Devices, IVDs, and Animal Health. The platform also includes harmonization organizations like WHO, ICH, VICH, and various trade associations such as AAFCO, IFPMA, CEFIC: APIC, IPEC, MedTech Europe, PhRMA, PDA, AABB, EFPIA, ESGCT, Team NB, and DITTA.