Works with research sites to facilitate IRB approval.
August 10, 2020
Develops suite of planning tools, including Study Oversight Plan, Clinical Monitoring Plan, enrollment plan, communication plan, contingency plan, start up and closure plan.
July 25, 2020
Creates study design that meets FDA study requirements, develop clinical protocols and amendments, create investigator materials, annual reports, abstracts, manuscripts and clinical study reports.
July 03, 2020