- API Development & Manufacture
- API Toxicology & GMP Supply
- Peptide & Protein Technology
- Custom Peptides
- GMP Peptide API
- Immunograde Peptides
- Modified Histones
- Protein Conjugation Technology
- Facilities and Equipment
- Contact Us – Peptide Quote
- API Radiolabelling
- Solid State Characterisation
- Solid State Services
- Drug Product
- Isotope Chemistry
- Pre-Clinical Safety Assessment
- Biocatalysis / selectAZyme™
- FLEXYTE™ Fluorescence Lifetime Assays
- Animal Free Chemokines
Method Development and Validation
We provide method development, optimisation and validation services for both API and drug products, to deliver analytical support in:
Our dedicated team of analytical chemists offer a unique blend of experience, expertise and focus to deliver reliable, information-rich methods to meet your exact requirements.
Working closely with clients, we deliver reliable and efficient stability-indicating methods. Use of automated method development software and emerging chromatography technology – such as UPLC™ – reduces method development times, providing smart separation solutions for the 21st century.
Validations are conducted under cGMP in compliance with ICH guidelines. The use of Empower 2 Method Validation Software allows us to streamline the method validation strategy. This brings the benefits of minimised time and cost for the validation process, whilst generating accurate and reliable data.