Manufacturing

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Review of SUT Adoption in Biopharma Manufacturing

The evolution of therapeutic modalities drives the adoption of single-use technologies.

Review of SUT Adoption in Biopharma Manufacturing

Why Are Pharmaceutical Companies Reluctant to Adopt Cloud Technologies?

Despite its understandable hesitancy, the pharma industry is facing a need for more widespread adoption of cloud-based solutions.

Why Are Pharmaceutical Companies Reluctant to Adopt Cloud Technologies?

Automating the Future of Fill/Finish

Given the criticality of fill/finish processes, it is clear that automation is the next technological step.

 Automating the Future of Fill/Finish

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Pharmaceutical Technology Europe

Forward-thinking manufacturers are recognizing the need for a more sustainable approach to containment design.

ePT--the Electronic Newsletter of Pharmaceutical Technology

Merck & Co. initiated a voluntary recall of 11 lots of its Haemophilus influenzae type B vaccine, Pedvaxhib, and two lots of its combination Haemophilus influenzae type B/ hepatitis B vaccine, Comvax.

ePT--the Electronic Newsletter of Pharmaceutical Technology

The US Food and Drug Administration posted on its website a Warning Letter it sent to Wyeth Pharmaceuticals regarding a journal advertisement for the company?s ?Effexor XR? antidepressant.

Perfect pumps for bio-processing and high-flow sanitary duties Watson-Marlow Bredel's 720 series peristaltic pumps are the perfect pumping solution for single-use or fixed bioprocessing systems. Featuring a smaller footprint than other pumps with a similar flow rate, 720 pumps provide low shear pumping up to 4,000 litre/hour and use sanitary LoadSure pumping elements for one minute maintenance.

After a good year of economic output growth, the EU chemical industry is losing momentum and a large drop in growth is expected for 2008 because of a cooling down of the world economy.

PTSM: Pharmaceutical Technology Sourcing and Management

Big Pharma's strategic push into biologics and continuing restructuring are among the highlights for 2007.

PTSM: Pharmaceutical Technology Sourcing and Management

Chi-wan Chen, deputy director of the Office of New Drug Quality Assessment (ONDQA) at the US Food and Drug Administration's Center for Drug Evaluation and Research, shares insight from FDA's pilot program that was designed to allow pharmaceutical companies to submit CMC information demonstrating application of quality by design.

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Congress Focuses on FDA Inspections of Foreign Drug Facilities; Medical Students Oppose Big Pharma's Influence on Campus; FDA Revises Postmarketing Reporting Requirements

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Pipeline Peril

The dynamics of the R&D pipeline could undercut recent CRO and CMO successes.

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Pharma Predictions

In honor of Pharmaceutical Technology's 30th anniversary, the editors conducted a survey of 320 readers last spring to discuss industry advances and future directions. Here are some of your foward-looking responses.

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Centrifuge processes many materials; New features for quality-management software; Unit simplifies powder discharge