Feb 24 2010 | Articles
For years, life sciences companies have struggled with the documentation burden associated with software validation. Over the past two decades, there has been much discussion about “paperless” validation.
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Mar 9 2009 | Products
Parenteral Contract Manufacturer
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Mar 9 2009 | Articles
Since the release of 21 CFR Part 11 in 1997, the validation and verification of electronic records has been at the forefront of the Information Technology (IT), Quality Assurance (QA) and Regulatory departments of the medical device and pharmaceutical industries.
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Mar 5 2009 | Products
Company's contract manufacturing facility now has the capability of producing injectable products via aseptic filling or autoclave terminal sterilization. Company specializes in the development and manufacture of products for pharmaceutical companies.
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Mar 5 2009 | Products
Contract biomanufacturing
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Mar 5 2009 | Products
Bubble elimination in a prefilled syringe offers many advantages for drug developers when deciding how a product is to be packaged for clinical studies or commercial distribution.
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Feb 11 2009 | Products
Bubble elimination in a prefilled syringe offers many advantages for drug developers when deciding how a product is to be packaged for clinical studies or commercial distribution.
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Jan 28 2009 | Products
A collision between technology and regulation is fast approaching. As pharmaceutical companies and their suppliers look for ways to cut costs, technology is leaping to the forefront. Leading the pack is the idea of outsourcing data centers to vendors using computer virtualization
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Mar 3 2008 | Products
Stability Optimiza-tion Services (SOS) is designed to assist drug manufacturers in optimizing their choice of parenteral product container/closure systems.
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Apr 4 2007 | Products
Company provides integrated lyophilized drug development and aseptic manufacturing services for a variety of large and small molecules. These include proteins and peptides, monoclonal antibodies (mAb), and high potency actives.
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