Throughout all phases of the product life cycle – R&D, clinical trials, manufacturing, advertising and even post-market surveillance – you must ensure the safety and effectiveness of your drugs and devices.
Bayside provides a full complement of experienced regulatory affairs professionals who understand your critical safety and compliance issues. Our talented managers and communicators:
- Ensure strict adherence to government rules and regulations
- Deliver thoroughly researched reports and presentations for your organization’s unique needs
- Track and report on adverse effects, in accordance with your company procedures
- Make an immediate, positive impact on your regulatory affairs projects and goals
A better approach to acquiring regulatory affairs talent yields better results for your business – and your consumers.
We’re Bayside Solutions. What can we do for you?
Contact us at 800.220.0074.
Bayside’s Regulatory Affairs Professionals
- Regulatory Affairs Associate
- Regulatory Affairs Manager
- Director Regulatory Affairs / Operations
- Regulatory Submissions
- Regulatory Publishing
- CMC Specialist
- Drug Safety Associate
- Drug Safety Coordinator