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  • Home
  • Stages
    • Late Discovery
    • Early Development
    • Late Development & Commercialization
    • Lifecycle Management
  • Services
    • Project Leadership & Business Solutions
    • Late Discovery & Investigative Research
    • Chemistry, Manufacturing & Controls (API & Drug Product)
    • Nonclinical Sciences
    • Clinical Strategy
    • Regulatory Strategy & Application Preparation
    • Quality & Compliance
    • Advanced Technologies
  • Leadership
  • News
  • Careers
  • Contact

CMC PHARMACEUTICAL DEVELOPMENT

NGT experts, together with our network of quality CROs, CDMOs and CMOs, provide drug substance, drug product and analytical strategic advice compliant with regulatory and ICH guidelines for:

  • API and drug product characterization
  • API route and regulatory starting material selection
  • Process development: Drug substance and drug product
  • Clinical trials material sourcing and vendor oversight
  • Genotoxic impurities, degradants and stability
  • Dissolution testing and bioequivalence
  • Manufacturing scale-up and batch-to-batch continuous process conversion
  • QbD, PAT process monitoring and control strategies
  • Technical due diligence
  • Analytical methods development and transfer
  • Technology transfer oversight

For further information regarding our CMC Pharmaceutical Development offerings

Please contact:
Alton Johnson, PhD
[email protected]

CASE STUDY – API and Drug Product Development Strategy

Situation

A start-up company with an asset ready to enter Phase III enlisted our support to create a product development report.

The company also requested support in presenting the CMC strategy, including steps to be taken to achieve their commercialization target cost of goods, to a potential partner.

Solution

A development report outline was created to assess status of the project end-of-Phase 2 clinical studies.

A digital validation lifecycle management solution was introduced to fulfill validation requirements for Stage 1, 2, and 3 including customized risk and knowledge management adjustments going forward.

A regulatory and technology development framework including levers to reduce cost of goods was provided to the potential partner.

Impact

API and DP development reports were drafted, providing risk assessment inputs, to guide completion of the CMC development in parallel with the Phase 3 clinical studies.

A gap assessment of information required for CTD submission was completed: critical process parameters, critical quality attributes, material attributes, regulatory starting material strategy.

A cost of goods reduction proposal was endorsed by the commercial partner.

Click here for additional Case Studies

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