Our dedicated team has vast experience in coordinating phase II to IV trials on both national and international scales. We can perform all stages of clinical trials – from feasibility to final study report – to the highest quality standards.
We have wide therapeutic experience, excellent cooperation with site staff, and in-depth knowledge of local requirements. Our core expertise and focus is in the South and South East Asia, however we are able to cover the whole of Asia and many other countries through our partner CROs. Our resourcing model provides both the flexibility and local knowledge of each country that the study requires.
Monitor plays a significant role to ensure the project success. As a company commitment to Clinical Research Excellence, we designed the role of our monitors to go beyond, than simply meeting the technical accuracy demanded by the research.
Our CRAs are trained to predict site management issues and proactively develop and implement solutions. CRAs undergo a thorough instructional regimen and are trained. This approach is employed from the earliest stages and throughout the conduct of the clinical study, to ensure the proper flow and responsiveness of the process.
All our monitors are full-time bilingual employees, equipped with laptops and are always available through mobile phones and internet when they are off site.
Whether helping your organization handle an overload of work on a single project or designing a full-service clinical program for your product, Croissance clinical trials management team has experience and knowledgeable staff members ready to assist you.
Our expertice includes:
Clinical project management
Ethics committee submission
Clinical monitoring and site management.
Clinical Trial Management System.
Investigator meeting planning.
Site selection and initiaton
Investigation product management
Quality training of clinical associates.
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