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Cortellis CMC Intelligence

Global chemistry, manufacturing, and controls (CMC) regulatory intelligence for drug development and market access.

Solution by Clarivate Plc
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Overview

Cortellis CMC Intelligence, from Clarivate, is a dedicated regulatory intelligence platform designed to simplify and accelerate access to global chemistry, manufacturing, and controls (CMC) regulatory information. Built for pharmaceutical and life sciences professionals, it serves as a single, authoritative source for CMC regulatory intelligence, helping teams reduce research time and navigate the complex requirements involved in bringing a drug product to market.

The platform addresses one of the most challenging aspects of drug development — ensuring that manufacturing and formulation processes meet the evolving regulatory standards of markets worldwide. By consolidating CMC regulatory content into one place, Cortellis CMC Intelligence enables regulatory affairs teams, CMC scientists, and compliance professionals to work more efficiently and with greater confidence.

Key Capabilities

  • Provides a single source of global CMC regulatory intelligence, eliminating the need to consult multiple disparate resources
  • Simplifies access to chemistry, manufacturing, and controls regulatory requirements across international markets
  • Reduces the time researchers and regulatory professionals spend gathering and verifying CMC-related regulatory information
  • Supports pharmaceutical teams in aligning drug development and manufacturing processes with current global regulatory expectations

Who It Is For

  • Regulatory affairs professionals responsible for CMC submissions and compliance
  • Pharmaceutical scientists and formulation teams requiring up-to-date manufacturing guidelines
  • Life sciences organisations seeking to streamline the path from drug development to market authorisation
  • Compliance teams managing regulatory requirements across multiple global markets

Cortellis CMC Intelligence is part of the broader Cortellis suite of life sciences intelligence solutions offered by Clarivate, a trusted provider of research and development tools for the pharmaceutical and healthcare industries. For more information or to discuss access options, teams can contact Clarivate's sales or customer service representatives directly.

Meta

Domain
Quality, Compliance & Regulatory
Subdomain
Regulatory Information Management (RIM)
Software type(s)
Database / Knowledge Base
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
PharmaBiotechCRO
Development stage(s)
ClinicalManufacturingPreclinical / Pre-Market
Target user(s)
Research ScientistQA / Regulatory Affairs
Compliance standard(s)
GxPICH