A controlled document distribution process - in which getting the right information to the intended recipients within a desired, or required, timeframe and being able to track delivery status and confirm receipt - is a challenge for regulated industries. Life sciences companies, regardless of whether they do business globally or regionally, continuously face many reporting obligations, a very prominent example being reporting on adverse drug reactions or adverse events.
Whether the data originates from marketed drugs or from clinical studies, the documents must be delivered to a variety of recipients within a predefined timeframe, using predefined methods of delivery and required formats. All this must take into account the relevant global, regional or local regulations, as well as recipients' internal business requirements.
A reliable, fully automated system allowing efficient management of reporting obligations that is not only accepted by all recipients but is also compliant with all applicable regulations is the preferred way of supporting such a process. To get the most out of a distribution solution, flexibility needs to be built into the system in numerous ways:
pharmasol's psiXchange establishes the relations between data from multiple sources, making your data actionable.