Analytical & Quality Research

Method development, impurity identification and release testing that support every synthesis and process project.

Analytics run alongside chemistry, not after it. Methods are developed for each project, and impurity data feeds back into route and process decisions.

Scope

  • HPLC / GC method development and validation
  • Impurity identification and tracking
  • Specification setting and release testing
  • Stability studies

Deliverables

  • Analytical method and validation report
  • COA, spectra and chromatograms

How a project runs

  1. 01
    Inquiry & CDA

    Share the target and requirements under a confidentiality agreement.

  2. 02
    Route Design

    Feasibility, route options, timeline and quotation.

  3. 03
    Lab Synthesis

    Synthesis with in-process analytics and progress reports.

  4. 04
    Pilot & Scale-up

    Process optimisation, safety review and pilot batches.

  5. 05
    Delivery & Supply

    Product, COA and documents; ongoing commercial supply.

Have a molecule in mind?

Send us the structure or CAS number, the scale and the timeline. We reply within one working day, and can sign a CDA first.

Start a Project