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Digital Health Products and Their Regulatory Challenges
Published in March 2026 Issue 03 (Vol. 14, Issue 3, 2026)

Abstract
Mobile health applications, wearable devices, telehealth platforms, artificial intelligence (AI) applications, and electronic health records have changed healthcare delivery through improving access, efficiency, and participation of patients. Regulatory affairs will have an essential part in assuring the safety, effectiveness, quality, and data security of digital health innovations as they expand and grow fast. By influencing how we classify products, evaluate risk, clinically validate, secure cybersecurity, improve interoperability, and evaluate post-market regulatory pathways, we seek to find a balance between innovation and patient safety.
Keywords: Artificial Intelligence (AI), Mobile Health, Quality Assurance
Authors (2)
Shubham.S.Wadate
YSPM’s YTC Faculty of Pharmacy...YSPM’s YTC Faculty of Pharmacy, SataraYSPM’s YTC Faculty of Pharmacy, SataraYSPM’s YTC Faculty of Pharmacy, Satara
View all publications →Aneri.V.Adsul
YSPM’s YTC Faculty of Pharmacy...YSPM’s YTC Faculty of Pharmacy, SataraYSPM’s YTC Faculty of Pharmacy, SataraYSPM’s YTC Faculty of Pharmacy, Satara
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Article Information
Published in:
March 2026 Issue 03 (Vol. 14, Issue 3, 2026)AJPHR3140002
AJPHR-01-000908
19-28
2026-03-20
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How to Cite
Shubham.S.Wadate & Aneri.V.Adsul (2026). Digital Health Products and Their Regulatory Challenges. American Journal of Pharmacy and Health Research, 14(3), 19-28. DOI:https://doi.org/10.5281/zenodo.19219652
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