Which are Site Management Organization Services?
We keep our processes and your projects under control through the
implementation and oversight of our in-house, updated, precise
Standard Operating Procedures (SOPs) or the Client’s SOPs if this is
your preference.ACTG-CRO provides SMO to help support both
principal investigators and sponsors. Learn more about the Clinical
Research Courses
Through our SMO service, we provide principal investigators with trained
CRAs II to assist with daily clinical trial activity and patient recruitment;
and sponsors to provide clinical trial site management and ethics
committee support.
We plan the studies and organize the meetings of the investigators in
our offices or at the Investigator's or in the place defined by the Study
Promoter.
Site Management Organization Services include:
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Study Management
IRB Management
Site contract, budget expense management
Enrolling and retaining participants, managing visits
Patient safety management
Safety and Adverse Events (AEs) Management
Ensuring Protocol Adherence
Ensuring Data Security
Quality control
Logistics management
Archiving Essential Documents
Archiving trial data
Data Collection
eCRF completion
Conclusion
SMOs specialize in running clinical research courses sites. Outsourcing
a clinical research trial to an SMO can help global pharmaceutical
companies, especially in setting up a business as an SMO, will minimize
their workload effectively and efficiently. Many numbers of hospitals,
experienced and well-qualified doctors, large patient pool emblematizing
chronic as well as infectious diseases, high savings in cost, and easy
recruitment of patients are leading to become a lucrative hub for
conducting global clinical trials.