Stridon provides first-class regulatory services to help expedite drug development within a complex and dynamic regulatory environment. Our services in this area include:
Includes preparation of Ethics Committee documentation and Investigator support for the submissions.
We have senior regulatory specialists on hand, dedicated to managing the ethics and regulatory approvals to ensure an efficient and timely start of your studies. Our experience in regulatory affairs covers the competent authorities in the UK and in Central and Eastern European countries (where this offering from Stridon is available either as a stand-alone service or as part of our site management services).
Our team are experienced regulatory professionals with the regional knowledge (including local language and culture) and contacts needed to communicate effectively with the appropriate regulatory agencies.
Global coverage, if required, is achieved through our network of regulatory service partners.
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Contact us now to learn more about our regulatory services and submission of clinical trial applications
