Sage Journals: Discover world-class research

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Research article

First published 2025-9

Navigating nutraceuticals regulation: A comparative assessment of the USA and India

Fazal M. Tai, Alishanaz I. Subedar, M. Hasan Harsoliya [...]

Journal of Generic Medicines: The Business Journal for the Generic Medicines Sector

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Research article

First published 2021-04

Regulating Generic Ophthalmologic Drug Bioequivalence—Envisioning Accessibility for Patients

Markham C. Luke, Darby Kozak

Journal of Ocular Pharmacology and Therapeutics

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Research article

First published 2009-8

Lessons from gefitinib-induced interstitial lung disease: Pharmacovigilance for erlotinib in Japan

Tsutomu Nishimura, Harue Tada, Masanori Fukushima

International Journal of Risk & Safety in Medicine

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Research article

First published 2009-11

Trialing plasma protein therapies for rare disorders: Thinking outside the box

Albert Farrugia

Pharmaceuticals Policy and Law

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Research article

First published 2006-04

Pills,Power,People: Sociological Understandings of the Pharmaceutical Industry

Joan Busfield

Sociology

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Research article

First published 2018-3

What to Know About Medicines With New Active Ingredients Approved in FY 2016 / 2016 in Japan and EU

Hideyuki Kondo, Agnès Saint-Raymond, Naoyuki Yasuda

Therapeutic Innovation & Regulatory Science

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Other

First published 2010-08

DNA Tests to Determine Ancestry Are Problematic;Direct-to-Consumer Genetic Testing Kits Require Pre-Market Approval;GAO Criticizes;FDA Management Practices;Yes,You Should Use the Rotavirus Vaccine;Prostate Cancer Vaccine Finally Approved;Companies Should Be Able to Discuss Off-Label Use of Drugs If the Information Is True;Counterfeiting Conviction Reversed;Huge Fine Assessed in Off-Label Promotion Case

Biotechnology Law Report

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Research article

First published 1999-3

Marketing Functional Foods: What Have We Learned? An Examination of the Metamucil,Benefit,and Heartwise Introductions as Cholesterol-Reducing Ready-to-Eat Cereals

Nancy M. Childs

Journal of Medicinal Food

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Research article

First published 2012-2

Patient-reported outcomes in the post-approval environment: Opportunities and challenges

Alex Mutebi

Pharmaceuticals Policy and Law

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Research article

First published 2018-6

The US Food and Drug Administration’s expedited approval programs: Evidentiary standards,regulatory trade-offs,and potential improvements

Joshua D Wallach, Joseph S Ross, Huseyin Naci

Clinical Trials

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