CPhI preview – Trinity Scientific: new standalone contract laboratory

Published: 25-Sep-2012
Regulatory Analysis

Provides a wide range of analytical services to the pharmaceutical industry

Trinity Scientific is the new standalone contract laboratory from the DDD group of companies, providing a wide range of analytical services to the pharmaceutical industry.

We can offer:

  • Method development, transfer and validation
  • Full ICH stability testing and storage
  • Analytical testing:
    • Chemicals, bulks, finished goods
    • Pharmacopeia testing: EP, BP and USP
    • Non-routine testing
    • Investigations
  • Companies:
  • Dendron Brands
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Trending Articles

  1. Chemistry, manufacturing and control (CMC) as key drivers for drug discovery success Embracing collaborative strategies not only accelerates drug development programmes but also fosters science-based milestone decisions, mitigates risks and prepares for successful market entry from the early stages of development, reports Frederick Duynslaeger, Senior CMC Writer at Ardena
  2. Overcoming CMC challenges in cell and gene therapy: part II Certara’s Dr Hien Anh Bruno, Associate Director, Chemistry, Manufacturing and Controls (CMC), and Dr Deven Shah, CMC Lead, propose mitigation strategies to address the CMC challenges inherent in producing cell and gene therapy (CGT) drugs
  3. Overcoming CMC challenges in cell and gene therapy: part I Certara’s Dr Hien Anh Bruno, Associate Director, Chemistry, Manufacturing and Controls (CMC), and Dr Deven Shah, CMC Lead, propose mitigation strategies to address the CMC challenges inherent in producing cell and gene therapy (CGT) drugs
  4. Innovating with purpose for safety and security of outcome Beyond the importance of increasing productivity and generating more output and value with the same input, new ideas and technologies from GEA take innovation a step further
  5. AskBio receives FDA Fast Track Designation for congestive heart failure gene therapy programme The fast-tracking allows the development and expedition of review processes for AB-1002, a gene therapy to promote production of a constituently active form of I-1c

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