A specific quality system, continuously adapted to your project:
NATURALPHA has established and is maintaining a high-level Internal Quality Assurance program:
Writing and updating Standard Operating Procedures and their appendices,
Implementing periodic Management Reviews and quality indicators,
Performing internal controls and audits,
Performing training sessions…
We create for your project its specific “Project Quality Plan” (PQP). This adapted “Plan” defines all quality aspects specific to your project:
Applicable procedures,
Qualification of subcontractors involved,
Qualification of investigational centers,
Audit plans,
Specific trainings required.
This policy, implemented from the creation of the company, allows us:
to build-up clinical trials with the maximal compliance with international standards (ICH EMEA FDA),
to continuously improve our quality management system,
to involve numerous investigators and patients across the world and still maintain the satisfaction of our customers, no matter how complex or large the clinical trial may be,
to limit development costs and pressure from pharmaceutical market, reducing the margin for failed trials and poor regulatory evaluation.
>> Successful R&D projects with the best cost-efficiency ratio in defined timelines