Learn about how we optimise experimental and analytical design in bioassay to help secure FDA approval

How we can support you:

365 days a year GLP & GMP Statistics
Same day draft reporting for routine GLP & GMP  statistical work
2 days, ready for use QA report for all GLP & GMP routine work
Guaranteed 100% QC check of every result
Fast, reliable service customised to your needs
Full process control support / trending if required
Reference bridging when required

Bioassay blog:

What is relative potency?

Health technology assessment blog