Pharmacy Times

APRIL 4, 2025

Mark Mulvahill, MBA, MSc, discusses the importance of microbial preservation and reference materials in pharmaceutical manufacturing and compounding pharmacies, highlighting their role in contamination control, regulatory compliance, and enhancing microbiological testing reliability.

Compounding Pharmacies 48

Compounding Pharmacies Compounding Pharmaceutical Manufacturing 48

Pharmacy Times

JULY 12, 2023

Analyzing the patent and trademark challenges faced by 503A compounding pharmacies.

Compounding Pharmacies 26

Compounding Pharmacies Compounding Pharmaceutical Manufacturing 26

Quality Matters

OCTOBER 13, 2021

In addition to standards for active pharmaceutical ingredients, USP also develops standards for the inactive ingredients (excipients) and other raw materials used in drug manufacturing. In a 2019 report on drug shortages, the FDA found that 62% of drug shortages occur because of quality issues in manufacturing.

Pharmaceutical Manufacturing 52

Pharmaceutical Manufacturing Adverse Reactions Prescription Filling Compounding 52

Quality Matters

AUGUST 3, 2023

While focuses on evaluating and establishing supplier reliability for pharmaceutical manufacturing companies and compounding pharmacies, its high-level elements of supplier qualification can also be applied to suppliers of foods and dietary supplement ingredients.

Packaging 52

Packaging Compounding Pharmacies Pharmaceutical Manufacturing Documentation 52