We offer solutions and support for every phase and form of clinical and medical research. We take pride in our research's efficacy, quality, and accuracy.
KM Clinical Research Group’s expertise enables us to assist our clients in tracking the outcome of their patients through new and investigational treatments and surgical interventions.
We take a collaborative approach to every project, working closely with our clients to understand their unique needs and develop customized solutions that deliver results.
At KM Clinical, we take a data-driven approach to medical research and development. We leverage the latest technologies and methodologies to ensure that our projects are efficient, effective, and impactful.
Our team of experts brings together a diverse range of skills and experience in the fields of medicine, science, engineering, and technology. We are passionate about what we do and are committed to improving the lives of our clients' patients.
We work with you to determine study objectives & purpose, the methods & procedures, a data safety & monitoring plan, and draft the subject informed consent.
A central IRB is used to ensure the study is safe & ethical. We will work with facility-specific IRB and ethics boards as needed.
Training will be provided for all study personnel. This includes principal investigators, sub-PI's, clinical research coordinators, and other study-related staff.
Online or PDF surveys and case report forms for data collection will be created to be completed by patients and/or providers. A HIPAA-compliant survey site and database will be used to collect and store all responses.
Monthly fee to ensure study protocol adherence and communications with study personnel. Includes quarterly study updates to all investigators and sponsors. 24/7 access to a HIPAA-compliant database to view study progress.
Yearly renewal of study with all involved IRB/ethics boards.
If patients are to be compensated for completing surveys, we will send them a gift card to the store or company of their choice.
All collected data will be analyzed and reports generated as needed. Reporting can be customized for C-suite, marketing, or research teams.
Publishing & presenting the results.
Includes writing the Abstract, Methods/Procedures, and Results sections of the manuscript. The main author(s) will be responsible for contributing to the Introduction/Background, Surgical or Technique Procedures, and Conclusion sections, as appropriate.
In the event reviewers request modifications to the manuscript these will be made and resubmitted for approval.
Format manuscript per journal's specifications. Includes cover letter to editor. Can be listed as corresponding author to facilitate communication between the research team and journal editors, reviewers, and readers.
Additional work outside of the above items will be billed at $500.00/hr. This may include interim reports, investor meetings, or C-suite presentations.