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:

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.