Critical review of EU BE guideline (Rev.1) [Regulatives / Guidelines]
Dear Helmut,
Thanks. But your anecdote is suited to deepen bad mood or to run screaming away.
Inscrutable are the Regulator's ways!
His spirit bloweth where it listeth.
(The holy Bible).
I don't know if this is not an over-interpretation. Lines 190-192 state what you find a good idea, and I also.
But reference medicinal product is defined above in lines 177-183 as "... must be a medicinal product ... on the basis of a complete dossier ...". And this term is used in lines 193-194.
❝ An anecdote from my side to lift your mood: [...]
Thanks. But your anecdote is suited to deepen bad mood or to run screaming away.
❝ Do you get the idea?
Inscrutable are the Regulator's ways!
His spirit bloweth where it listeth.
(The holy Bible).
❝ 4.1.2 Reference and test product (page 6, lines 193-194)
❝ 'When variations to a generic product are made, the comparative medicinal product for the bioequivalence study should be the reference medicinal product.'
❝ IMHO, this a very good idea - nothing was stated about it in the 'old' NfG, ...
I don't know if this is not an over-interpretation. Lines 190-192 state what you find a good idea, and I also.
But reference medicinal product is defined above in lines 177-183 as "... must be a medicinal product ... on the basis of a complete dossier ...". And this term is used in lines 193-194.
—
Regards,
Detlew
Regards,
Detlew
Complete thread:
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