Senior Director, Drug Safety and Pharmacovigilance
Top 50 Pharmaceutical Company
“Sentrx processes the adverse event reports from all of our marketed as well as investigational products. Activities include assessment for regulatory reporting, data entry, narrative preparation and medical review; preparation of periodic reports for marketed products; and basic IT infrastructure and safety database hosting.”
“Sentrx has performed well in delivering these services. We have been working with Sentrx for over three years and together have developed a compliant pharmacovigilance program for our company. We have been able to keep our internal staff at a minimum, even as our company grew. If we kept these activities in house, I estimate we would need to double our staff.”
“Our companies communicate frequently, which is essential to a successful relationship. Regularly scheduled weekly teleconferences, quarterly face-to-face meetings and daily conversations regarding operational issues allow our company to remain in control of pharmacovigilance decisions even though we have outsourced this function.”
“Sentrx is one of a handful of service providers that works exclusively in safety. This allows them to be focused on these issues and provide a higher level of expertise compared to other CROs. Also, Sentrx has an outstanding IT team that is very familiar with the uniqueness of safety databases and provides excellent service to their clients.”
“I highly recommend Sentrx to other companies. In fact, we recently renewed our contract for an additional three-year term.” |
