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Debbie ★ India, 2010-03-17 14:41 (5946 d 00:36 ago) Posting: # 4930 Views: 3,530 |
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Hi, Please suggest usage working standard for bioequivalence studies for ANVISA Submission. Is this mandatory to use only compendial reference standards (Brazil/USP/EPCRS) for conducting method validation and bioequivalence studies as per the resolution 899, point no 1.4 The approch of using a working standard which was standardized against a compendial reference standard with suffient characterization data and COA is acceptable to ANVISA. Please share any experiance with ANVISA. If acceptable what are the documents to be submitted as a part of regulatory submission. Thanks&Regards |
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Ramesh ☆ India, 2010-03-18 12:52 (5945 d 02:25 ago) @ Debbie Posting: # 4932 Views: 2,818 |
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Hi ❝ Is this mandatory to use only compendial reference standards ❝ (Brazil/USP/EPCRS) for conducting method validation and bioequivalence ❝ studies as per the resolution 899, point no 1.4 As per my experience we should have a valid C of A of reference standards used in the BA/BE study. In addition to this the supporting documents such as purity of the compound, charactersation of compound if any etc. I hope this is usefull. Regards, Ramesh.V — with regards, Ramesh |
