Efficiently learn about a disease
- How do you onboard MSLs to a therapeutic area?
- Do you rely on one MSL to provide training or must staff self-educate?
- While traveling, is there 24/7 access to key facts?
ScienceMedia has a searchable library of over 16,000 topics designed to teach your staff about diseases, treatments, patients' journeys, and clinical approaches.
- 24/7 access to content from any device through Google-like search
- Updated and current content
- Continually expanded disease coverage
- Cloud-based (IT and LMS administrators are NOT required)
- Empower your CRAs — Improve their site interactions
- Free your medics and monitors from making outdated PowerPoints
How do you train Medical staff on product and clinical details?
- Do you send papers to your Medical Affairs professionals and expect them to retain all of the information?
- Do you onboard and teach product details through live meetings?
- Is your foundational training accessible and reusable, well beyond the initial training?
ScienceMedia develops start-of-the-art education for Medical Affairs professionals.
- The training can be used in foundational training, and again later for reinforcement and quick reference.
- Clinical papers and package inserts are annotated with instructional media to emphasize important points.
- Everyone receives the same doctorate-level training.
How are your MSLs supporting pivotal clinical trials?
- How do you provide clinical trial objectives, statistics, and conduct?
- How are details layered regarding vulnerable subject populations?
- What is the MSL's purpose at each site visit?
ScienceMedia has a searchable library of over 16,000 topics designed to teach your staff about diseases, treatments, patients' journeys, and clinical approaches.
- ScienceMedia can onboard your teams for the conduct of your clinical trials using 24/7 accessible education available in SMi Source
- ScienceMedia develops protocol-specific education for sites through SMi Trial, so your MSLs and CTLs can concentrate on protocol nuances and real-world subjects at site visits.
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Let's talk about destroying your trials' deviations and transforming your stakeholders' clinical mastery