Additional Services
We are focused on sharing our expertise and building industry partnerships, for international and regional clinical research.
Partnerships at the Core of Medicine
At Siron Clinical, we believe that our wealth of experience benefits the clinical research industry and medical community. Our services aren’t limited to just monitoring, project management, quality assurance, and submission. We build strong partnerships to support additional clinical trial needs.
Additional Services
Consultancy
Statistics and data management (in collaboration with a partner)
IWRS (in collaboration with a partner)
Our Services
Customizable FSP
Our Expertise, On Your Terms
Customizable Functional Service Provider (FSP)
Project Management
A Seamless Extension of Your Organization
Project Management
Clinical Monitoring
Expert Support for Your Investigators and Teams
Clinical Monitoring
Quality Assurance and Control
Accuracy and Integrity
Quality Assurance and Control
Regulatory Submissions
Globally Minded, Local at Heart
Regulatory Submissions
Additional Services
Partnerships at the Core of Medicine
Additional Services
How is Clinical Trial Success Defined in Europe?
Bringing a product further down the development pipeline often requires conducting clinical research in Europe. In the EU, the Clinical Trials Regulation harmonizes the submission process, but local requirements are still varied and specific to each country, and cultural differences can be challenging.
What defines clinical trial success in Europe? Download our RFI on to discover more about our insights, approach and experience.
Experience Matters
As an international contract research organization (CRO), we offer unparalleled knowledge, support, guidance, and experienced clinical research professionals to the biotechnology, life science, and medical device industries. We are committed to leading the development of new and advanced treatments by offering a range of CRO clinical trial services, from Customizable FSP to full-service.