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For manufacturers, the focus is less about choosing between formats, and more about building platforms that can scale intelligently, adapt to future modalities, and remain compliant under increasing regulatory scrutiny

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doi: 10.1089/biores.2018.0025 [DOI] [PMC free article] [PubMed] [Google Scholar] 52.Mabilleau G, Mieczkowska A, Irwin N, Flatt PR, Chappard D

The spokesperson told MNT the FDA monitors the safety of drugs throughout their life cycle, including post-approval

Women should maintain open communication with their healthcare providers about reproductive health changes throughout treatment

Therefore it requires medical evaluation and treatment of the underlying condition