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OTC Drug Testing

Brand Equivalence to Innovation

Ensure monograph compliance to the U.S. Pharmacopoeia (USP) and European Pharmacopeia (Ph. Eur.) by partnering with Avomeen’s industry-leading OTC testing and development lab. With decades of experience in generic drug testing and bioequivalency, our talented and dedicated Ph.D. scientists are uniquely qualified to formulate improved, novel, and National Brand Equivalent (NBE) products in addition to providing indispensable analytical support.

When you’re in the OTC product development stages, get the testing you need from Avomeen’s OTC lab to guarantee you release a stable and safe product to market.

Service Specialties

Why Partner with Avomeen?

Our expert scientists will ensure your products meet cGMP and full monograph requirements, labeling under 21 CFR 201.66, and identify any contaminants or failure root causes. Here are some additional benefits from partnering with us utilizing our OTC testing services:

  • cGMP compliant, FDA registered, DEA licensed
  • Consultative, flexible, and responsive staff
  • Project customization to your specific needs
  • Experience in solving difficult analytical and formulation challenges
  • Delivery within tight timelines
  • Up-to-date regulatory knowledge to ensure compliance

Let’s work together to achieve your vision

Ready to get started? Click Get a Quote, or talk to an expert first if you’d like help in defining your project scope.