Benefits for a Physician to collaborate with Medsol

  • Maria Vasconcelos, RN, the Director of Research has over 25 years of experience in Research as a study coordinator and 8 years as a Clinical Research Monitor.
  • Susan Coldiron, LPN, has 8years experience as a study coordinator
  • We locate studies that are of interest to our physicians and review your charts/database and advertise to enroll potential subjects
  • We will attend Investigator meetings with physicians and be present during monitoring visits and Audits.
  • The Regulatory Process, protocol budget will be completed by Medsol
  • Study visits can be completed at Medsol or we can come to the Investigator’s office if approved by the Sponsor
  • You, the Principal Investigator are not obligated to accept a study unless you are comfortable with the Benefit/Risk ratio and safety of our subjects.
  • 24 Hour Emergency Availability On-Call system to filter calls prior to contacting
  • the physician
  • Screening and subject enrollment, obtaining initial informed consent and managing the informed consent process will be completed by Medsol
  • All protocol assessments that can be delegated to a study coordinator are completed by Medsol. Including scheduling visits, reminder calls, completing source documents and CRFs
  • Regulatory oversight will be initiated and maintained at Medsol
  • Study Product, Lab supplies and study specific documents are housed at Medsol
  • Scheduling of visits with subjects will be arranged to the convenience of physician
  • There is no interruption in workload to your staff within your busy practice