Outsourcing Regulatory Affairs White Paper

Outsourcing Lifecycle Maintenance to a Dedicated FSP Regulatory Affairs Partner

Pharma and biopharma developers face many regulatory requirements when bringing a new drug or device to market. However, these requirements extend beyond the approval stage, necessitating ongoing compliance and maintenance across the product lifecycle.

To ensure adherence to regulations and the continuous supply of drugs to target markets, outsourcing regulatory affairs (RA) maintenance activities through a functional service provider (FSP) partnership is worthwhile.

In this white paper, you will learn more about:

• Regulatory requirements throughout a product’s life, post-approval
• The challenges of lifecycle maintenance
• The benefits of outsourcing lifecycle maintenance activities to an FSP partner