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Technical parameters and documentation standards Manufactured under Current Good Manufacturing Practice regulations Adheres to documented USP criteria for laboratory-grade water Individual batches verified for endotoxin and sterility markers Certificate of Analysis available for laboratory audit trails Maintaining research compound stability and efficacy Unpunctured vials should be maintained at controlled room temperature

[DOI] [PubMed] [Google Scholar] 304.Taracanova A., Alevizos M., Karagkouni A., Weng Z., Norwitz E., Conti P., Leeman S.E., Theoharides T.C

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