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.
Summit Clinical Research has successfully completed a strategic investment in Houston Research Institute and strengthened its executive team with the appointment of Dr. Mazen Noureddin as Co-Chairman of Summit's Board of Directors and the additions ...
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Wednesday, March 13, 2019
SGS welcomed the preliminary data from a controlled human infection trial with FluGen’s investigational M2SR vaccine.
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Wednesday, September 26, 2012
Almac is pleased to announce the successful inspection of its Clinical Services operations located in Craigavon by the UK Medicines and Healthcare products Regulatory Agency (MHRA).
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Wednesday, February 11, 2015
Dishman Group has announced the successful completion of an inspection by the U.S. Food and Drug Administration (FDA) for its Netherlands site. The inspection, carried out by an USFDA investigator, was planned for 5 days but lasted 3 days, starting ...
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Thursday, December 18, 2014
Hovione today announced that the U.S. Food and Drug Administration (FDA) performed a Pre-Approval Inspection to its plant in Loures, Portugal, covering two NDA filings. At the conclusion of the inspection, the FDA issued a Form 483 with three ...
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Hovione today announced that its API plant in Cork, Ireland has successfully passed a pre-approval inspection by the US Food and Drug Administration (FDA).
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Envigo has announced that its Research Models and Services facility in Hyderabad, India has been granted full accreditation by the AAALAC International Council.
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The FDA is establishing a public docket to invite discussion of issues related to the adoption of continuous manufacturing by the pharmaceutical industry.
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Wednesday, August 26, 2020
SubjectWell is working with pharmaceuticals to recruit patients for Phase 2 and Phase 3 COVID-19 vaccine trials.
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SubjectWell has developed a growing patient registry of individuals in the US interested in participating in clinical trials for a COVID-19 vaccine as these trials become more widely available.
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Wednesday, December 11, 2019
SubjectWell has partnered with data-sharing platform Human API to provide free medical record retrieval to clinical trial sites and sponsors.
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Tuesday, January 30, 2024
Suanfarma announced a strategic rebranding initiative. All of this is aimed at reinforcing the importance of Suanfarma as a global player in the healthcare sector, both as a distributor of APIs and as a CDMO company in the production of active ...
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Medical marijuana has not been proven to work for many illnesses that state laws have approved it for, according to the first comprehensive analysis of research on its potential benefits.
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Wednesday, January 18, 2017
Robust competition in the private marketplace is resulting in increasingly higher rebates and discounts on medicine prices, according to a new study by the Berkeley Research Group (BRG). The study is among the first to examine the share of ...
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Tuesday, December 29, 2015
Roughly half of all surveyed global and U.S. pharmaceutical teams report involving key opinion leader (KOL) management or medical science liaison (MSL) teams in their investigator-initiated trial (IIT) proposal collection processes.
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