? Pharmacovigilance and Drug Safety Software – Safeguarding Patient Health with Smart Tech

Pharmacovigilance and Drug Safety Software refers to digital platforms used by pharmaceutical companies, CROs, and regulatory bodies to monitor, manage, and report adverse drug reactions (ADRs) and ensure medication safety throughout its lifecycle.

? What It Does:

• ? Collects adverse event data from patients, providers, and trials

• ? Analyzes patterns and signals that indicate potential safety concerns

• ? Reports findings to regulatory authorities (like the FDA, EMA)

• ? Automates compliance workflows and global reporting standards (E2B, MedDRA)

? Why It Matters:

• Prevents large-scale health risks and recalls

• Enhances public trust in drug therapies

• Supports global regulatory compliance

• Enables faster and more accurate decision-making in drug development

? Who Uses It:

• Pharmaceutical & Biotech companies

• Contract Research Organizations (CROs)

• Healthcare regulators

• Hospitals and clinical trial networks

? Market Momentum:

With the rise in global drug launches, regulatory tightening, and AI integration, this market is expected to grow significantly—fueled by increasing pharmacovigilance outsourcing and cloud-based software adoption.