Regulatory Affairs

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