Dietary Supplements

PROSAR is the leading provider of adverse event processing for dietary supplement manufacturers and we can help you implement an Adverse Event Reporting (AER) process to comply with the Dietary Supplement and Nonprescription Drug Consumer Protection Act.

PROSAR provides:

• 24/7 call center staffed with experienced pharmacists and RNs
• Extensive experience in preparing MedWatch 3500A reports for submission to FDA

PROSAR's services help you to:

• Acquire peace of mind knowing that the Dietary Supplement and Nonprescription Consumer Protection Act reporting requirements are fulfilled
• Realize cost savings by leveraging PROSAR's Adverse Event Reporting (AER) infrastructure
• Provide brand protection through access to comprehensive AE documentation to defend against claims
• Optimize product life cycles through ongoing post-market surveillance and timely, informed decision-making