Medi-Vantage President Authors Chapter: Global Medical Device Marketing Strategy
Working closely with medtech regulatory colleagues is a key role for medical device marketing.
“The question is: how can medtech marketing de-risk the selection of countries and regions to support company executive strategy?” said Ms. Shepherd.
“Close collaboration with our regulatory colleagues ensures that a global market assessment is performed to identify the countries and regions that are commercially viable,” she continued. “A market segment analysis is critical to the opportunity and strategy when the delivery of care is different from US and European models. I was asked to write this chapter by the Regulatory Affairs Professionals Society (RAPS) to be sure that all medical device companies, large and small, have the market assessment information they need to avoid unnecessary expense, delays, inefficiencies and possible failures to obtain approvals.”
Contact us. Global market assessments can be performed at costs as low as $3,000.
Key sections of the chapter:
Global Executive Strategy Development for Medical Device and Diagnostics Companies
Global Marketing Support and Analysis for Executive Strategy Decision Making
Regional Strategy Development
Market Segmentation and Classification of Regional High-To-Low Regulatory Barriers
How to Prioritize Segmented Markets for New and Existing Products
Global Advertising and Promotion Regulations
Direct to Consumer Advertising Trends for Europe and the US
KOL Development and the Sunshine Act
Human Factors Usability Testing Informs Regulatory Strategy
Market Research to Understand the Continuum of Care outside the US
The book Global Medical Device Regulatory Strategy can be purchased from RAPS by clicking here.