Transferring Inventions to Commercial Business. 

We provide complete spectrum of services in the drug development program for our global Partners consisting of formulation development, analytical development, stability evaluations and technology transfer.

In the pharmaceutical industry, “technology transfer” refers to the processes that is needed for successful progress from drug discovery to product development to clinical trials to full-scale commercialization or it is the process by which a developer of technology makes it’s technology available to Commercial Partner who will exploit the technology.

Key stages of the process include data collection, data review, regulatory impact with particular emphasis on any change approvals, analytical validation, pilot or full-scale process batch and stability data.

scientist doctor hand holds virtual molecular structure in the lab as medical concept

Our Products :

  • Product Dossiers in CTD Format
  • Product Development
  • Contract Manufacturing
  • Clinical Trials
  • Regulatory Affairs

CRIMSON has a sound understanding of the global regulatory requirements and we provide regulatory services to facilitate all stages of drug development with a strategy to obtain efficient pathway towards required regulatory approvals.

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