We provide a comprehensive range of clinical trial, site certification & patient recruitment services.
We provide regulatory consultation & quality assurance services to companies regulated by the US FDA, EMA & similar agencies in other countries.
Our qualified project managers & experienced consultants provide regulatory information and quality assurance for successful project outcomes.
We help train drug and device manufacturers in FDA audit preparation and conduct mock FDA audit at their premises.
We provide comprehensive range of quality assurance and regulatory CxP compliance services to the pharmaceutical, medical device, biotechnology, dietary supplement and other FDA-regulated industries
For any information on the training agenda and logistics, please call +102 410 501 5777 , +102 877 566 4981 or email: info@fdamap.com