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News Headlines   Processing & QC
Homepage > Processing & QC News

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Device to 'revolutionise' inhaled drug testing
07-May-2008 - UK-based Cambridge Consultants has developed a portable instrument which it says could "revolutionise" the way airborne drug delivery devices are tested.

Bioprocessing holds back Millipore in Q1
07-May-2008 - Continued weakness in the market for products used in the manufacture of biologic drugs was the main reason why Millipore experienced a 'challenging' quarter, according to CEO Martin Madaus.

Double-strength digoxin recalled in US
06-May-2008 - A heart medication sold by Mylan Laboratories in the US has had to be recalled, after it emerged that some doses may contain twice the intended dose of active ingredient.

Watson's OAI lifted and Goa manufacturing transfer on track
05-May-2008 - The US Food and Drug Administration (FDA) has withdrawn its long-standing block on the manufacture of new products at Watson Pharmaceuticals' facility in Davie, Florida.

IMA records boost in profits
05-May-2008 - Italy-based IMA has posted a 30.3 per cent increase in net operating profit for the 2007 calendar year, taking the total to $108m.

Merck warned by FDA over vaccine plant failings
05-May-2008 - The US Food and Drug Administration (FDA) has sent Merck & Co a warning letter saying it has failed to correct a number of manufacturing deficiencies at its main vaccine manufacturing plant in West Point, Pennsylvania.

Non-allergenic latex glove gets the nod
29-Apr-2008 - A new type of latex glove developed by Yulex Corp that is less allergenic for medical and research staff has been given a green light by the US Food and Drug Administration (FDA).

ELGA makes rental an option for water purification
28-Apr-2008 - ELGA Process Water has launched its new All-in-Pack water treatment solution for pharmaceutical manufacturers wishing to reduce both capital expenditure and associated running costs.

OSCS detection may protect heparin supplies
24-Apr-2008 - International research suggests that a simple in vitro bioassay, in addition to procedures currently in place, would help secure the global supply chain for heparin and reduce the risk of patients being exposed to harmful contaminants.

FDA links contaminant to adverse events: issues warning to China facility
24-Apr-2008 - The US Food and Drug Administration (FDA) has revealed evidence linking the heparin contaminant with the series of reported adverse reactions, and has also now issued a warning letter to the Chinese facility at the centre of the safety scare after completing its inspection.
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