We enable global clinical development teams to rapidly translate and share pharmacovigilance information, such as SUSARs (suspected unexpected serious adverse reactions), SAEs (serious adverse events), hospitalization reports, and discharge summaries, within a centralized collaborative workspace. With the ability to quickly and securely collect, track, translate, and share safety data from investigative sites with internal and external stakeholders, the safety reporting process is radically accelerated.
TransPerfect’s Trial Interactive solution traffics safety notifications and distributes alerts in real-time, ensuring that sites, sponsors, and CROs remain fully apprised of the latest information and data.
Collect and store cases received (ADRs, medical information, product complaints, non-case calls)
in a 21 CFR Part 11 compliant, validated, web-based global database.
TransPerfect can establish and staff new call centers to handle incoming calls – in any language. We can also supplement existing call center resources by handling overflow call volume or by providing over the phone interpretation services with specialized medical interpreters to help serve callers in over 170 languages.
TransPerfect’s Business Process Outsourcing program helps you construct a communication strategy to fit your patients’ ongoing needs.
Whether your needs are temporary or ongoing, our services include: