Scope of Information

Regulatory Information at your Fingertips

Tarius end users are primarily healthcare industry professionals who are responsible for the regulatory dialogue between their company and the national authorities, for example U.S. Food and Drug Administration (FDA) or Japan’s Pharmaceuticals and Medical Devices Agency (PMDA).

Regulatory Activities Covered

Tarius supports you as a regulatory professional by providing in one place all relevant information from the national authorities if your company wants to develop, register, manufacture and market your product(s), including information concerning:

  • Clinical Trials (Good Clinical Practice, GLP/GCP),
  • Access to unapproved Therapeutic Products (Compassionate Use, Expanded Access and Treatment Programs),
  • Application Procedures,
  • Fees,
  • Pricing and Reimbursement,
  • Good Manufacturing Practices (GMP),
  • Labeling and Packaging,
  • Good Distribution Practices (GDP),
  • Safety/Adverse Event Reporting/Risk Management (Pharmacovigilance/Vigilance),
  • Import/Export of healthcare products,
  • Advertising to consumers/healthcare professionals.

Healthcare Products Covered

The Tarius services cover a wide range of healthcare product categories such as:

  • Prescription Drugs (Rx),
  • Over-the-Counter Drugs/Non-Prescription Drugs (OTC),
  • Biotechnology and Biological Products,
  • Gene Technology,
  • Homeopathics Medicines,
  • Medical Devices,
  • In-Vitro Diagnostics (IVDs),
  • Combination Products/Drug Delivery Products,
  • Biosimilars and Generics,
  • Narcotic (Controlled) Drugs.

Tarius turns information into actionable intelligence by publishing data in value-added formats, such as Cross-Country Tables and Expert Summaries.