Sestron provides an experienced Clinical Research  team to conduct
Protocols according to GCP/ICH Guidelines and Sponsor
specifications. We ensure there is a clear understanding of the
Protocol and that Trial expectations are met according to the
agreed objectives.

Sestron ensures timely Sponsor/IRB Regulatory Submissions.

Sestron Research ensures that all Subjects are qualified as defined
in Inclusion/Exclusion Criteria per Protocol and are treated in
compliance with industry safety, confidentiality, and heath

Sestron ensures  each Subject:
Fully understands the Informed Consent Process and that
this process continues throughout the duration of the study
Is supervised by the Principal Investigator at each visit
Is encouraged to complete Trial participation
|  Sestron Clinical Research  |  833 Campbell Hill St. Suite 230  |  Marietta, Ga 30060  | Telephone: 770-795-7905  |  Fax: 770-795-7978  |