Pharmaceutical Outsourcing covers news of importance to the contract services segment of the pharmaceutical industry.
Collected from the most trusted on-line resources, these news stories are chosen and published here based on their relevance to the pharmaceutical industry.
Topics of interest typically include: mergers and acquisitions, service additions, new capabilities, personnel changes, news from the FDA and other international regulatory and standard-setting agencies, and new outsourcing contracts and deals.
If you are looking to stay up-to-date with the news in your industry, this resource is vital for your industry knowledge.
Jones Packaging Inc. recently invested in a fully automated solid dose plastic vial filling line to address the growing market demand for convenience packaging. The line is operating in the company’s Contract Packaging Services facility in the ...
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Tuesday, September 11, 2018
SGS announced it is investing over $1.7M to expand its North American biopharmaceutical testing capabilities at its Lincolnshire facility in the northern suburbs of Chicago, Illinois.
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Tuesday, October 03, 2017
Phenomenex has introduced SecurityCAP; a mobile phase and solvent waste safety system for HPLC and UHPLC Systems.
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More than one third of pharmaceutical industry professionals are not confident that they will meet serialization deadlines in the US and Europe, according to new industry research.
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Wednesday, November 10, 2021
Anavasi Diagnostics announces it has been awarded $14.9 million from the NIH Rapid Acceleration of Diagnostics initiative.
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Tuesday, November 18, 2014
New Oncology announced today that it has entered into a collaboration with the National Cancer Centre Singapore (NCCS). Under this agreement, New Oncology will apply its proprietary [2]diagnostic platform ‘NEO’ that enables physicians to select ...
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Monday, December 11, 2017
Thermo Fisher Scientific's Ion Torrent Oncomine Myeloid Research Assay interrogates DNA mutations, RNA fusion transcripts and gene expression levels.
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RSSL is to launch several new services to the biopharmaceutical sector, covering all aspects of the EMA regulatory guidelines for safety, quality and efficacy of biopharmaceuticals. Services will be GMP compliant where appropriate.
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Monday, February 04, 2019
ValGenesis announced a New Jersey-based leading contract manufacturer of pharmaceutical drugs has chosen ValGenesis's 100% paperless VLMS to manage its validation lifecycle process.
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Wednesday, November 11, 2015
The Biotechnology Industry Organization (BIO) and BioNJ have commended Governor Chris Christie for signing critical legislation to create a pathway for the substitution of interchangeable biologic medicines.
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The FDA has sent a warning letter to Tris Pharma after investigators found the company had failed to properly investigate batch failures and establish quality control procedures.
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Laureate Biopharma is pleased to announce its successful collaboration with Dyax Corp. for process development and cGMP production of a new treatment candidate for hereditary angioedema (HAE). The drug candidate, known as DX-2930, is a fully human ...
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Friday, December 13, 2013
Thomas Feinberg, PhD, Catalent Pharma Solutions’ Director of Development and Analytical Solutions, is to present at the forthcoming “Suitability and Compatibility for Packaging and Delivery Systems
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TTP and New England Biolabs (NEB) announce that they have established a non-exclusive partnership to offer services to molecular diagnostic technology developers.
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Thursday, February 08, 2018
Bluebee and New England Biolabs have partnered to provide a secure and convenient data processing solution for NEB's NEBNext Direct target enrichment technology.
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