Recognized as a PM360 Elite 100 Winner for 2026
Recognized for innovation in compliant social media management for regulated industries.
Pharmacovigilance
Every comment on a pharma social post is a potential AE report. MarketBeam monitors 24/7, flags automatically, and documents everything — keeping you compliant with ICH E2D and FDA reporting timelines.
AI identifies patient-reported symptoms in a comment on your LinkedIn post. All four AE elements present T+0 minutes
Structured AE case created with comment text, timestamp, channel, post context, and reporter information. T+1 minute
Pharmacovigilance team receives alert via email and in-platform notification with full case documentation. T+2 minutes
Social team responds using pre-approved AE acknowledgment language from the Response Guide — no ad-libbing. T+15 minutes
Full interaction logged immutably. Ready for PV team follow-up and regulatory reporting within required timelines. T+15 minutes — Case Closed
Why MarketBeam
Generic social media management tools were never designed for pharma compliance. Here’s why regulated life sciences companies choose MarketBeam.
| Capability | MarketBeam | Generic Social Tools | Custom-Built Solutions |
|---|---|---|---|
| Veeva PromoMats Integration | ✓ Certified | ✕ | Custom Build |
| MLR Review Automation | ✓ Built-in | ✕ | Months to Build |
| Adverse Event Detection | ✓ AI-powered | ✕ | Limited |
| FDA Audit Trail | ✓ Automatic | Manual export | Varies |
| Controlled Employee Advocacy | ✓ Native | No compliance controls | ✕ |
| Social Media Response Guide | ✓ In-app | ✕ | Separate tool |
| Multi-Regulatory Framework | ✓ FDA, EMA, PMDA | ✕ | High cost |
| Time to Deploy | ✓ Weeks | Weeks but no compliance | 6–18 months |
