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.
ResearchDx, LLC of Irvine, California today is pleased to announce the purchase, build-out and relocation to our state of the art 30,000 sq. foot facility in Irvine California. The custom designed facility will support our continued expansion of in ...
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ICON plc, a global provider of drug development solutions and services to the pharmaceutical, biotechnology and medical device industries, has announced research showing many pharmaceutical and clinical research organizations (CROs) support the use ...
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New industry research reveals that more than one third, 36%, of pharmaceutical manufacturers and contract packagers are not currently preparing for global serialization requirements, despite impending deadlines.
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Despite R&D-focused pharmaceutical executives recognizing digital as the primary driver to be more patient-outcome focused, only half of them are currently adopting digital, according to a new report from Accenture.
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Thursday, September 07, 2017
According to new industry research more than half of industry professionals believe that the cost of implementing serialization is the greatest hurdle to compliance.
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The newly combined CRO specializes in collaborative partnering for global clinical trials.
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REPROCELL has been producing clinically relevant human induced pluripotent stem cells (hiPSCs) by controlling the process of donor recruitment to seed stock hiPSC and encompassing donor eligibility with different geographical regulatory agencies.
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REPROCELL announced the launch of its US FDA compliant Good Manufacturing Practice (GMP) Master Cell Bank (MCB) manufacturing service for human induced pluripotent stem cells (iPSCs).
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Thursday, January 29, 2026
REPROCELL announced the launch of StemEdit, its clinical gene editing services and new gene-edited iPSC product lines leveraging OpenCRISPR-1™, an AI-designed genome editing system licensed from Profluent.
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Tuesday, November 10, 2020
Repositive has expanded its global network of CRO partners with the addition of Pharmatest, a CRO providing clinically predictive preclinical efficacy services for oncology and skeletal diseases.
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More than 1 in 5 sexually active teen girls have used the morning-after pill — a dramatic increase that likely reflects that it's easier now for teens to buy the emergency contraceptive.
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Wednesday, March 30, 2016
Greater acceptance of biosimilar medicines in a growing number of therapy areas and an active pipeline of 56 new products in clinical development are expected to deliver total savings of as much as $110 billion to health systems across Europe and the...
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Global post-marketing pharmacovigilance and medical information market is expected to reach USD 5.3 Billion by 2022, according to a new report by Grand View Research, Inc.
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Research and Markets has announced the addition of the "Pharmaceutical Contract Manufacturing & Contract Research Market, 2014 - 2025" report to their offering.
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Thursday, October 05, 2017
Many pharmaceutical manufacturers are switching to continuous production from batch methods.
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