multi-therapeutic research organization for inpatient and outpatient trials Phases I-IV. Ventavia takes great pride in our efficient turnaround time for all start-up activities such as regulatory submissions and contract/budgets negotiations. Our subject recruitment methods include an involved method of pre-screening to ensure a high quality of participant. Ventavia’s team adheres to all ICH GCP standards and are committed to expedited data entry, in-house quality assurance, prioritizing subject safety, and maintaining a high level of professionalism through the entire process. In the development of new medications, Ventavia understands the investigative site’s role is vital. We embrace all challenges and opportunities that arise within clinical research and are dedicated to ensuring each trial is conducted with the highest industry standards.