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Facilities

Business & Regulation Facilities

Keep It Clean

| Stephanie Vine

The technology behind cleanrooms is well over 50 years old. Is it time for a makeover?

Manufacture Quality & Compliance

Turning Failure into Success

| Stephanie Vine

We should look to Warning Letters – and the subsequent solutions – to benefit from the blunders of others.

Manufacture Facilities

Fumigation of the Future

| Andrew Ramage

A choice of fumigants are available for fumigating microbiological safety cabinets and high-level containment rooms. One substance that is still used in the industry is formaldehyde, but given that formaldehyde is toxic, carcinogenic and corrosive, you’d be better looking for alternatives.

Manufacture Facilities

Embracing Rapid Microbiology

| Tim Sandle

Microbiological approaches are faster and more advanced than ever before – so why on earth isn’t the pharma industry using them?

Business & Regulation Facilities

Sterility Fears at the NIH

| Stephanie Vine

How did the NIH get it so wrong – and how can it move on?

Business & Regulation Facilities

Investigating the de-agglomeration profiles of dry powder inhaler formulations

In this paper, the authors describe the use of laser diffraction to analyse dry powder behaviour.

Manufacture Facilities

Fill & Finish of the Future

| Susan Dexter

The technology has barely changed over the last 30 years – surely, it’s time for some long overdue innovation.

Discovery & Development Facilities

Laser diffraction and automated imaging: complementary techniques for nasal spray development

Nasal spray products are increasingly valued for delivering systemic as well as locally-acting therapies, most notably hormone and migraine treatments

Manufacture Facilities

Terminal Inertia

| Jeanne Moldenhauer

It is clear that terminal sterilization is the gold standard for sterile drug manufacture, so why are companies so reluctant to pursue it?

Manufacture Facilities

Aseptic ‘Warehouse’ Danger

| James Agalloco

Is there a ‘safe’ hold time for sterilized items? And, if so, how can those hold times be reliably validated?

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