Renejix – Small Molecule CDMO (USA)

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Commercial Solutions

Pharma innovators rely on our expertise and broad capabilities to producing essential clinical trial drug supplies. Many of our clients begin in the preclinical phase and often extends through Phase II. We deliver agile, lean, and comprehensive clinical supply services, to streamline the process and costs for our clients.

Robust Offerings for:

Clinical Trial Supply Capabilities:

Our facilities and experts are adept at manufacturing clinical supplies, even as small as 1 kg for oral solid dosage forms.

  • Wet granulation
  • Dry granulation
  • Fluid bed technology, including the use of solvents
  • Spray Drying
  • Hot Melt Extrusion
  • Encapsulation & Softgels
  • Tablet compression
  • Film coating
  • Stick pack filling — tablets and granules — for pediatric trials
  • Liquid/suspension clinical supplies
  • Powder-in-bottle (PiB) dosage forms

Dedicated Formulation Support:

    • Our formulation experts act as your technical partners throughout your clinical development program.
    • A dedicated formulator ensures continuity and leverages the knowledge acquired during development for effective scale-up production.

Comprehensive Analytical Support:

      • Our services extend to all aspects of analytical development during clinical trials.
      • Equipped with UPLC and HPLC capabilities, along with a full range of dissolution equipment, we also offer analytical method validation services from Phase I to commercial.
      • Our stability services encompass all ICH conditions and other specialized requirements.

At Renejix, we are committed to providing seamless, end-to-end clinical trial supply services, ensuring that your clinical pathways are as smooth and efficient as possible.

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