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It operates under the 503A compounding framework established by the Drug Quality and Security Act (DQSA) of 2013, which means it can prepare individualized prescriptions for specific patients but is not registered as a 503B outsourcing facility and is therefore not subject to the more stringent current Good Manufacturing Practice (cGMP) standards that govern 503B facilities

Reconstitute at 20 mg/mL to bring the same dose down to 50 units

Easy Mammalian Expression and Crystallography of Maltose-Binding Protein-Fused Human Proteins

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The local refined map and model has entry number EMD-18994 and PDB-8R84