Tag: biosimilar approval

Biosimilar Approval: How the FDA Reviews Biologic Alternatives in 2026

Biosimilar Approval: How the FDA Reviews Biologic Alternatives in 2026
wayne Holloway in: Medications 16 January 2026

The FDA's 2025 guidance streamlines biosimilar approval by replacing costly clinical trials with advanced analytical data, accelerating access to lower-cost biologic alternatives for cancer, arthritis, and diabetes. Learn how the process works and what's still holding it back.

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Team-Based Care: How Multidisciplinary Teams Are Changing Generic Prescribing
Team-Based Care: How Multidisciplinary Teams Are Changing Generic Prescribing

Team-based care transforms how generic drugs are prescribed by bringing together doctors, pharmacists, and nurses to improve safety, adherence, and cost savings - especially for patients with multiple chronic conditions.

Published ON: 18 Feb
Labor Cost Differences: Generic vs Brand Drug Production Explained
Labor Cost Differences: Generic vs Brand Drug Production Explained

Generic drugs cost far less than brand-name drugs not because ingredients are cheaper, but because labor costs are structured differently. Learn how scale, regulation, and global production shape the real cost of your prescriptions.

Published ON: 9 Feb
Edema in CKD: How Diuretics, Salt Restriction, and Compression Therapy Work Together
Edema in CKD: How Diuretics, Salt Restriction, and Compression Therapy Work Together

Edema in CKD is caused by fluid buildup from failing kidneys. Managing it requires a three-part strategy: the right diuretics, strict salt restriction, and compression therapy. Learn how each works-and how to use them safely.

Published ON: 7 Feb
Hyponatremia and Hypernatremia in Kidney Disease: What You Need to Know
Hyponatremia and Hypernatremia in Kidney Disease: What You Need to Know

Hyponatremia and hypernatremia are common, dangerous complications in kidney disease. Learn how sodium imbalances happen, why standard treatments fail, and what actually works to protect your health.

Published ON: 8 Feb
How the FDA Ensures Generic Drug Quality During Manufacturing
How the FDA Ensures Generic Drug Quality During Manufacturing

Discover how the FDA maintains strict quality standards for generic drugs through cGMP regulations, unannounced inspections, and rigorous testing. Learn about the five key control areas, global comparisons, and real-world impact on drug safety and affordability.

Published ON: 4 Feb

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