— Service one —
Site Management Organization SMO
Site Management Organization
As a site management organization, we provide services to the investigator and clinical site. We deliver operational and administrative support services to the clinical investigator at a research site/practice. This includes everything from handling regulatory and compliance activities to managing patient recruitment and data collection. We also provide support with the study start-up, monitoring and closeout. Some of the services include:
Contract and Legal Agreement
Training of site staff
Documentation preparation (such as informed consent form (ICF), tracking form, recruitment materials, source documentation)
Submission of clinical trial to institutional or central review board
Regulatory Management
Subject recruitment and follow up.
In house monitoring
Quality Assurance
— Service Two —
Consulting Services
Consulting Services
We understand you may not need a full-on SMO but an organization that can help get your site back on track or initiate your study site. We at Dumog Research are available to design/provide the service you will need to meet your site goals.
Our aim is to drive meaningful and sustainable impact in the medical industry. We provide the capabilities and processes needed to ensure long-lasting viability for the solutions we provide. Our team of experts, who are familiar with the challenges in a wide range of therapeutic indications, have a clear understanding of the pharmaceutical industry. As such, we will assess your needs carefully and design a program to meet your goals.