Before developing a proposal or selecting a site, expert
team of CTCVN will review and evaluate the research protocol, develop
scientific supervision, and act as a focal point for research centers, hospitals,
investigators
CTCVN connects with research groups of hospitals across the
country. so we can quickly collect data, assess feasibility, and determine
which study site is best for your clinical trials.
CTCVN has a team of experienced staff who can advise and
carry out the submission of documents in compliance with current regulations.
Patient safety and regulatory compliance are our primary goals when conducting
clinical trial studies.
Our team of experienced professionals is available to assist
you in all areas of clinical trial related legislation.
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