Regulatory Intelligence by DR Evidence is a software-as-a-service (SaaS) solution designed to streamline the process of regulatory intelligence gathering. It eliminates manual efforts spent on navigating multiple regulatory websites and analyzing extensive PDFs. The platform aggregates regulatory documents from the FDA's CDER and CBER divisions and the European Medicines Agency (EMA) into a single searchable interface. Users can refine their searches using filters and keywords to quickly locate comprehensive and precise regulatory content relevant to their needs.

Key Features

Unified Regulatory Document Access Centralized access to FDA (CDER and CBER) and EMA documents in one platform.

• Eliminates the need to visit multiple regulatory websites individually.
• Covers a broad range of regulatory content in one place.

Advanced Search and Filtering Powerful keyword search combined with filtering options to narrow down results effectively.

• Helps users quickly find the most relevant regulatory documents.
• Saves time compared to manual scanning of documents.

Comprehensive and Precise Content Identification Ensures users capture all the necessary regulatory information accurately.

• Avoids missing critical regulatory updates or changes.
• Supports compliance and regulatory strategy decisions.

Benefits

Time Efficiency Reduces hours spent on manual regulatory research by providing a streamlined workflow.

• Access multiple regulatory sources instantly.
• Filter and identify relevant documents with ease.

Improved Regulatory Compliance Stays up to date with the latest FDA and EMA regulations by comprehensive document coverage.

• Supports risk management and regulatory adherence.
• Enhances decision-making with reliable intelligence.

User-Friendly Interface Simplifies access to complex regulatory information with an intuitive platform design.

• Reduces training and onboarding time.
• Enables teams to focus on analysis rather than data gathering.