UK adopts EC variations regulation
Guidance has been published in the UK regarding a new European variations regulation that comes into effect on 1 January 2010. More...
After 20 years, ICH tops harmonization efforts
Pharmaceutical Technology talks to FDA's Justina A. Molzon about current discussions with international regulators, and how, after 20 years of harmonization activities and the common technical document, the ICH has benefited regulatory authorities. More...
Businesses miss out on green opportunities
European business leaders are missing opportunities to reduce their environmental footprint and drive efficiencies through document governance, according to research from Ricoh, an electronic solutions provider. More...
Sanofi-aventis plans participation in Russian project
Sanofi-aventis has signed a memorandum of understanding (MoU) with Prominvest, a fully owned subsidiary of the Russian State Corporation Rostekhnologii, confirming its intent to participate in the Pharmpolis Project. More...
Cash boost for UK bioprocessing
The private industry has been urged to join a public sector commitment fund in the UK to advance manufacturing R&D in bioprocessing, following the investment of approximately £9 million from two UK research councils. More...
USP revises standard to prevent medication errors
The US Pharmacopeial Convention (USP) has posted a proposed revised standard for what should and should not appear on the ferrules and cap overseals of medication vials. More...
Podcast: Vetter Development Service Chicago
In order to minimize risks and take advantage of opportunities, you need comprehensive know-how and years of experience. Vetter, as a specialist in the aseptic filling of injection systems, can manufacture preclinical, Phase I and Phase II clinical batches from its new facilities in Chicago. We invite you to find out more about Vetter Development Services USA Inc. More...
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Product Profile |
Watson Marlow |
Peristaltic Pump Technology
Peristaltic pumps are at the centre of many single-use biopharmaceutical processes and medical/surgical instruments. Their non-contacting design makes them uniquely suited to these applications, providing lower contamination risks and reduced validation requirements.
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On Demand Webcast |
Just Systems |
Complex Documents in the Pharmaceutical Industry Made Easy
Complex Documents in the Pharmaceutical Industry Made Easy
Documents are created just about everywhere in the pharmaceutical industry. To manage interrelated documents, collaboratively created and updated, versioned and published to different targets can often turn into a nightmare. With XML authoring, recurrent tasks such as applying repetitive changes to similar documents or assuring quality for cross-referencing, can finally be automated.
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Latest peer-reviewed research |
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