• Act as your Permittee who assumes all legal liability for your product in the United States.  

• File all regulatory documents with the US regulatory authorities, which include, but are not limited to: drafting letters, study design, protocols/final reports, Outlines of Production, potency test design and validation, labeling, etc.

• Identify study partners for conduct of required clinical studies

• Plan, institute, and complete clinical studies

• Interact with the US regulatory authorities on your behalf regarding submissions and any concerns the manufacturer or the regulatory authorities may have

• Provide marketing and distribution services for your product if requested

We invite you to find out how we might help you to comply efficiently with USDA regulations to obtain a U.S. Veterinary Biological Product Permit to market your product in the U.S. Please contact us by email at info@VBPSLLC.com