Manufacturing

Cynthia A. Challener is a contributing editor to Pharmaceutical Technology.

Articles

Pressures to accelerate current and next-gen therapies are challenging traditional microbiological testing models.

Microbiological Testing: Time is of the Essence

GS1 US published new guidelines in preparation for the serialization and traceability requirements associated with DSCSA.

GS1 Releases New DSCSA Guidelines

UPS entered into a definitive purchase agreement to acquire Marken, a provider of supply-chain solutions for the life-science industry.

UPS to Acquire Marken

Agnes Shanley is senior editor of Pharmaceutical Technology.

The pharmaceutical industry has weathered its share of “black swan” events.

Tracking Potential Threats

Vendor selection and materials testing are complex enough, but in today’s volatile environment, risk mapping and monitoring are also crucial.

Managing Risk in Raw Material Sourcing

In 2009, the International Pharmaceutical Excipients Council introduced an Excipient Information Package that includes a product requirement datasheet, site quality overview, and site and supply chain security overview.

Standardized Templates Can Help Make the Job Easier

Adeline Siew is editor for Pharmaceutical Technology Europe. She is also science editor for Pharmaceutical Technology.

The proliferation of counterfeit medicines is nothing new to pharma; however, the scale of the problem seems to be escalating.

The Cost of Counterfeits

GENCO, a FedEx Company, introduces a multi-tenant warehouse model in Milton, Ontario, and Memphis, Tennessee.

Multi-Tenant Warehouse Option Aids Healthcare Companies

Recipharm launched a showcase line to demonstrate the company’s new serialization solutions.

Recipharm Launches Serialization Showcase Line

Marken announced the opening of a new depot and logistics operations center in Argentina.

Supply Chain