General Info
2011 RAPS provides the following benefits to event attendees:
- Monitor advances in related area(s) of expertise
- Network with colleagues and potential clients of all professional levels
- Access information from a range of international agency and expert representatives
- Contribute to the advancement of the regulatory profession
Learning Objectives
At the conclusion of this event, you will be able to:
- Produce methods to safely and effectively regulate a range of healthcare products in compliance with organizational and Government agency requirements worldwide
- Propose ways that current and anticipated future policy will drive regulatory issues for a range of healthcare products
- Analyze scientific and emerging technologies advancements and their potential effect on the regulatory profession and healthcare development worldwide
- Summarize the relationship between regulatory and business operations
- Describe various compliance concepts, issues and requirements throughout the product development lifecycle for a range of healthcare products.
Who Should Attend
Departments:
|
Regulatory
Compliance
Clinical
Quality
Research & Development
|
Laboratory Science
Legal
Compliance
Business Development
Validation |
Job Functions:
Mid-level Management
Executive-level Management
Project Management |
Risk Management
Crisis Management
Training/Staff Development |
Product Lines:
Pharmaceuticals
Biologics
Combination Products |
Foods and Dietary Supplements
Medical Devices
In vitro Diagnostics |
Learning Levels: Basic, Intermediate, Advanced