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Manufacturers of ingredients used as excipients in pharmaceuticals have faced some regulatory problems with a series substances known as 'atypical actives'. Related news |
Authorities seek injunction against Actavis in USThe US authorities are turning up the heat on Icelandic generic drugmaker Actavis over manufacturing problems at the New Jersey plant which makes its recalled Digitek brand of the cardiac drug digoxin. DSM agrees to Deretil management buyoutDSM Deretil, the chemical side-chain manufacturing operation of DSM's anti-infectives unit, is to go it alone through a management buyout. PharmaForm's EPAS aims to make particle processing less of a grindPharmaForm's new EPAS particle engineering technology, launched at this year's AAPS in Atlanta, US, may help drugmakers improve the solubility of insoluble actives without some of the costly and time consuming processing steps used by traditional methods. UK report calls for nano regulationsThe UK Royal Commission has issued a report on the spread of nanomaterials, stating that “urgent action [is] needed on testing and regulation”. |
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eClinical specialist etrials Worldwide saw its losses quadruple in the third quarter on the back of a dip in revenues and financial charges, including a $4m asset impairment charge related to goodwill.
One of the obstacles to the development of Poland’s clinical research market is due to be removed next month, according to local consultancy firm Polish Market Research.
Recent European legislation designed to increase the number of children in clinical trials has had a positive impact in ensuring that paediatric patients are included in medicine testing.
US company Smithers Group has launched a formulation services company to tap into the emerging trend towards outsourcing of drug development among pharmaceutical companies.
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Globalisation
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Mergers and acquisitions
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SAFC talks continuous processingMike HarrisManaging Director UK and Ireland, Sigma Aldrich, Vice President - SAFC Pharma |