Pharmaceutical Regulatory Services
PRS, Inc., headquartered in Princeton, New Jersey, USA, is a privately held company founded in 2000 that specializes in global regulatory and pharmacovigilance intelligence and consulting. They support projects worldwide, providing expert guidance to pharmaceutical and biotech clients, and operate through a network of experienced consultants and strategic partners across all continents. Their services include pharmacovigilance consulting, regulatory consulting, and access to their proprietary online database GRID, which contains global pharmacovigilance requirements for over 150 countries.
Industries
Nr. of Employees
small (1-50)
Pharmaceutical Regulatory Services
Princeton, New Jersey, United States, North America
Products
Online pharmacovigilance intelligence database (proprietary)
A proprietary web application that compiles pharmacovigilance and regulatory requirements across more than 150 countries into modules (Pre-Authorization, Post-Authorization, Notifications) with tabular and printable views and a notification system.
Online pharmacovigilance intelligence database (proprietary)
A proprietary web application that compiles pharmacovigilance and regulatory requirements across more than 150 countries into modules (Pre-Authorization, Post-Authorization, Notifications) with tabular and printable views and a notification system.
Services
Advisory services on pharmacovigilance requirements, gap analysis of pharmacovigilance documentation, and delivery of intelligence summaries.
Gap analysis and preparation of international registration and market access plans based on global regulatory intelligence.
Provision of subscription access to an online database of pharmacovigilance and regulatory requirements covering over 150 countries, with modular views and real-time notifications.
Advisory services on pharmacovigilance requirements, gap analysis of pharmacovigilance documentation, and delivery of intelligence summaries.
Gap analysis and preparation of international registration and market access plans based on global regulatory intelligence.
Provision of subscription access to an online database of pharmacovigilance and regulatory requirements covering over 150 countries, with modular views and real-time notifications.
Expertise Areas
- Pharmacovigilance intelligence
- Global regulatory strategy and intelligence
- Regulatory monitoring and change management
- International registration and market access planning
Key Technologies
- Web-based regulatory intelligence platform
- Online pharmacovigilance requirements database (multi-jurisdiction)
- Real-time notification/email alert system
- Tabular and printable/mobile-optimized data views