I have some doubt regarding fixing limitation of release specification and end of life specification for finished dosage forms in pharma industry. What basis the criteria is fixed. Help me in this regards.
Hi, let me try to help you. I hope this paper will be helpful.
Thanks for your reply. The articles are very helpful.
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kindly reply me. Thanking you in advance.
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Please go through my Abstract. I can also share a proposed Thesis Outline.
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DOS version.
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