At Scantox’ Quality Control and Analytical Development Laboratories within our Pharmaceutical Development & Analytical division we offer the following services:
- Pre-formulation work e.g. pH-solubility profile and log P
- Analytical method development
- Release testing for pre-clinical trials
- Stability stress testing
- Robustness testing
- Analytical method validation
- Cleaning method validation
- QC release testing of products for clinical trials (Certificate of GMP Compliance_Human Investigational Products – DK IMP 10000944)
- Stability testing at all ICH conditions and regulatory guidelines to establish shelf life of product
- Quality Control testing of marketed products (Certificate of GMP Compliance_Human Medicinal Products – DK H 10000947)