Bioanalytical Services
LC-MS/MS method development, validation and sample analysis to GLP, with Eurofins.
What this covers
Bioanalytical work is delivered with Eurofins as NAMA Bio-Center’s bioanalytical partner, under GLP and international regulatory standards.
LC-MS/MS method development and validation
In accordance with GLP and international regulatory standards.
Precise sample analysis
For pharmacokinetic parameters, supporting standard, partial replicate, and full replicate BE study designs.
QC, documentation and traceability
Comprehensive bioanalytical QC, documentation, and data traceability to ensure audit readiness and data integrity.
SFDA-structured reporting
Preparation of complete bioanalytical reports structured for SFDA review and regulatory submission.
Our bioanalytical services ensure dependable pharmacokinetic data that underpins confident regulatory decision-making.
Ready to run your BE programme in the Kingdom?
Tell us the molecule, the dosage form and the timeline you are working to. We will come back with a study design and a schedule.