Our ACRP-certified monitors have earned a well-deserved reputation for providing companies -- like yours -- with detail oriented, and efficient monitoring services.
We have worked with drug products in all phases (I thru IV) of development.
A rapid turnaround time is provided on trip reports, and we're accustomed to maintaining an on-going relationship with the study unit(s), to keep the sponsor and the site(s) up to date on study progress.
Our standard operating procedures include outlines and methods for all visit types, including:
- pre-investigational site visits (PISV)
- site initiation visits (SIV) site monitoring visits (SMV)
- site closure visits (SCV)
We follow Good Clinical Practice Standards, and ICH guidelines.
