DUBLIN--(BUSINESS WIRE)--The "Product Registration and Navigating the Approval Process with Regulatory Authorities in Asia Pacific, Europe, Middle East and The Americas" conference has been added to ResearchAndMarkets.com's offering.
This seminar will provide an overview and in-depth snapshot of the product registration and approval process for Asia Pacific, Europe, Middle East, United States, Canada, Mexico and South America. Employees who will benefit include all levels of management and departmental representatives from key functional areas and those who desire a better understanding or a "refresh" overview of the registration and approval process in select countries, including:
- Regulatory Affairs Management
- Regulatory Affairs Specialist
- Auditors
- Compliance Officer
- Compliance Specialist
- Clinical Affairs
- Quality Assurance Management
- Marketing & Sales
- Distributors/Authorized Representatives
- Legal Counsel
- Engineering/Technical Services
- Operations/Manufacturing
- Consultants
- Learning Objectives
Areas Covered:
- Get assistance with medical device registration and medical device approval
- Learn how to access new markets and obtain medical device approval in all the countries listed
- Complete your registration in order to obtain medical device approval as efficiently as possible while realizing that some markets/countries will be more challenging
- Navigate the regulatory system, achieve product registration, and access the medical market
- In a group setting, review and discuss pain points, challenges and workable regulatory and compliance solutions
For more information about this conference visit https://www.researchandmarkets.com/research/s7ws25/product?w=4
