Letter of Authorization (LOA) Request for a Drug Master File (DMF)

Bio-Techne is committed to supporting your cell therapy’s progress into the clinic. Many of our GMP reagents have a Drug Master File (DMF) on file with major regulatory bodies, facilitating your IND filing and swift approval. To view GMP proteins that have an existing DMF on file, visit GMP Proteins for Cell Therapy Development and Manufacturing.  

Please complete this online request for a Letter of Authorization (LOA) to receive information about a product's DMF. Please note we have existing DMFs for several Bio-Techne products. For products that do not have an existing DMF, our team will review your request and get back to you. For all LOA requests, a Bio-Techne representative will reach out to you.