Our expert scientists. Your drug discovery pipeline.
With Aquila, you can be confident that your results stand up to external scrutiny. We ensure our data is of the highest quality and suitable for peer review or meeting regulatory requirements.
We have a quality assurance audit programme in place, which includes study-based, process-based and annual facility inspections. All our staff are GCP and/or GCLP trained, and we work to GCP for Labs (GCLP) standards.
Our SOPs are in accordance with the Integrated Addendum to ICH GCP E6(R2): Guideline for Good Clinical Practice E6(R2), and we work to the guidelines ‘Reflection paper for laboratories that perform the analysis or evaluation of clinical trial samples’ (Ref. EMA/INS/GCP/532137/2010, EMA, 2012).
Please get in touch to discover how we guarantee our high-quality results.