Having recognized a fundamental disconnect between manufacturers and the ever-changing life sciences ecosystem, US Drug and Device Register was created to function as a liaison between these disparate entities. The firm’s fundamental principle seeks to assist clients in answering the all-important sales questions: How can I succeed in the complex and evolving US healthcare market? US Drug and Device Register supports both Global and US based clients looking to succeed in the US healthcare market. We work with organizations of all sizes and stages in the life cycle from those just emerging to Fortune 500 companies across the life sciences industry.

Our areas of expertise include but are not limited to:

  • Pharmaceutical
  • Prescription Digital Therapeutics
  • Medical Devices
  • Durable Medical Equipment
  • Consumer Packaged Goods
  • Med-Surg Supplies
  • Dental
  • Chiropractic
  • Food Service

Results that Matter

Since our inception, US Drug and Device Register, Inc. has achieved unparalleled success in helping our clients succeed in the US life sciences markets. Our approach to client services includes successful interface with the key stakeholders:

Drug Regulatory/Registration

  • Compendiums
  • Pricing strategies
  • Gov’t Regulatory Agencies/FSA-HSA/EMR

Government/Military

  • Federal Supply Schedule/GSA
  • Governmental Bidding
  • Public Health/340B

Managed Care

  • Commercial
  • Medicare
  • Medicaid

Healthcare Institutions

  • Hospitals
  • Long-Term Care
  • Prison Systems
  • Clinics
  • Integrated Delivery Networks

Distribution

  • Drug Wholesale
  • Med-Surg
  • DME – Durable Medical Equipment
  • Home Health