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INTERPHEX Puerto Rico 2011
October 20, 2011–October 21, 2011
San Juan, PR USA
AAPS 2011
October 23, 2011–October 27, 2011
Washington DC, USA
IVT's 17th Annual Validation Week
October 24, 2011–October 26, 2011
Philadelphia, Pennsylvania
CPhI Worldwide 2011
October 25, 2011–October 27, 2011
Frankfurt, Germany
4th West Coast Forum on Clinical Supply Chain Management
December 6, 2011–December 7, 2011
Burlingame, California

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FDA Proposes Enhancing Search Criteria for Inspections Database
FDA may consider whether to add specific search criteria (e.g., those that would enable product-specific or violation-specific searches) to its inspections database to make it user-friendly and improve data analysis. The idea was included in a list of eight draft proposals for increasing transparency that the agency published on Oct. 3, 2011. 
Private Equity Firms to Acquire PPD for $3.9 Billion
The CRO Pharmaceutical Product Development (PPD) will be acquired by the Carlyle Group and Hellman and Friedman in a deal valued at approximately $3.9 billion. PPD shareholders will receive $33.25 per share in cash, and PPD will become a privately held company after completion of the transaction. 

EMA Invites Feedback on Biosimilar and Vaccine Concept Papers
EMA released two concept papers for consultation that address the need to revise existing guidelines on biosimilar medicines and influenza vaccines. 
Takeda Completes Nycomed Acquisition
Takeda Pharmaceutical Company has completed its acquisition of Nycomed for EUR 9.6 billion ($12.9 billion) on a cash-free, debt-free basis. In addition, Takeda has named Frank Morich, Takeda’s executive vice-president of internal operations (Americas/Europe), as Nycomed’s CEO. 
Servier and Galapagos Form Cancer Collaboration
Servier and the Belgium-based biotechnology company Galapagos are embarking on a multiyear strategic alliance to develop new cancer therapies. As a result of the alliance, Galapagos could receive milestone payments of more than EUR 250 million ($332 million). 
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Bioprocess analyzer ensures proper protein production conditions
Roche’s Cedex Bio Bioprocess Analyzer is a continuous random-access instrument that enables the safe and reliable determination of chemical and biochemical parameters in aqueous solutions. The compact desktop system is designed to
perform metabolite screening and substrate analysis of bioprocesses. Its testing capabilities include photometric testing and electrolyte testing. The instrument allows users to measure as many as 14 parameters simultaneously, out of 28 programmable tests, per sample. The unit also enables continuous loading and unloading of diverse cup types. |
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Abbott Japan and Eisai have launched Humira (adalimumab) prefilled syringe 20mg/0.4mL, a fully human anti-TNF-α monoclonal antibody for the treatment of polyarticular juvenile idiopathic arthritis patients with low body weight, on Sept. 29, 2011. The product received manufacturing and marketing approval from Japan’s Ministry of Health, Labor, and Welfare on July 1, 2011, and was subsequently listed on the National Health Insurance price list on Sept. 12.

The CDMO Aesica has announced plans for further growth and expansion following an investment from Silverfleet Capital, a European private-equity firm. Subject to regulatory approval from the German authorities, which is expected to
occur within the next four weeks, Silverfleet Capital has agreed to make a majority investment in Aesica, and members of the Aesica executive team have reinvested in a large minority stake in the company. Financial support will be provided by Lloyds Bank Corporate Markets Acquisition Finance, HSBC, and Yorkshire Bank. Additional corporate support will continue to be supplied by PricewaterhouseCoopers, Ernst & Young, and Ward Hadaway.
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AstraZeneca has settled its patent-infringement litigation against Handa Pharmaceuticals regarding Handa’s proposed generic version of AstraZeneca’s Seroquel XR (quetiapine fumarate) extended-release tablets. The agreement ends the patent-infringement litigation that followed Handa’s submission of an abbreviated new drug application for a generic version of Seroquel XR.
Under the settlement, Handa does not dispute that both patents asserted by AstraZeneca in the litigation are valid and enforceable. As part of the agreement, AstraZeneca has granted Handa a license to enter the US market with generic Seroquel XR on Nov. 1, 2016, or earlier, depending upon certain circumstances. Seroquel XR is protected by patents and other exclusivity rights that range from March 2012 to November 2017.
AstraZeneca and Handa will file a proposed consent judgment with the US District Court for the District of New Jersey requesting that the court dismiss the pending legal action between AstraZeneca and Handa. The remaining Seroquel XR patent-infringement litigation remains ongoing.
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Braun Medical, a healthcare supply company, has installed Werum Software & Systems’ PAS-X operational system at its production facility in Sempach, Switzerland. PAS-X will be used to optimize the manufacturing of liquids.
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Covance, one of the world's largest and most comprehensive drug development services companies, now offers a comprehensive and integrated set of CMC Pharmaceutical Development Services, including API development and supply, preformulation and formulation,
analytical and stability, and regulatory documentation services. This offering is built on the combination of top-five pharma expertise, facilities, and decades of excellent client service record. Covance is committed to helping you reduce the time required to development milestones and improve your molecule hit rate.
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The CDMO Catalent Pharma Solutions and Toyobo Biologics, a supplier of bioreactors, have agreed to copromote Catalent’s proprietary GPEx technology in the Japanese market. GPEx technology is used for mammalian cell-line development.
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Single-us disposable filling needles are now available for Bosch and TL fillers. Disposable needles eliminate cleaning, and cross contamination concerns and reduce issues with bent needles. Available presterilized or autoclave ready. Needles are available
in sizes ranging from 1.2mm to 5.5mm inside diameter. Click to learn more about single-use needles and complete single-use filling solutions from Bosch Packaging Technology.
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The Johnson & Johnson (J&J) subsidiary McNeil-PPC and its affiliate McNeil MMP have acquired of full ownership of the J&J–Merck Consumer Pharmaceuticals joint venture in the United States from Merck Sharp & Dohme. The joint venture will be renamed McNeil Consumer Pharmaceuticals and will continue to market products
under the Pepcid, Mylanta, and Mylicon brands. In addition, J&J, through its McNeil Consumer Healthcare Division (McNeil Canada), has acquired from Merck Canada its partnership interest in the Canadian joint venture. McNeil Canada will continue to market and sell Pepcid, 222, and Fleet Enema in Canada. Ownership of the manufacturing facility in Lancaster, Pennsylvania, will transfer to McNeil-PPC.
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See how the latest advances in instrumentation provide you greater power and ease in the analysis of genotoxic impurities. Gain an understanding of how the enhanced sensitivity of the Xevo TQD with positive and negative switching allows for faster analysis of impurities. Learn how the ability to reduce matrix interference using RADER helps speed up the method development process.
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The CMO Lonza Group’s acquisitions subsidiary LG Acquisition has extended the expiration date for its tender offer for 100% of the outstanding shares of common stock of the biocides company Arch Chemicals to Oct. 14, 2011. The tender offer is at a price of $47.20 per share in cash, without interest and less any required withholding taxes pursuant to a merger agreement between Arch Chemicals, Lonza, and LG Acquisition, dated July 10, 2011. The tender offer has been extended because the conditions are not expected to be satisfied as of the previously scheduled expiration date.
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LC/MS/MS Speed Beyond Comparison
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Lundbeck, a pharmaceutical company, and the pharmaceutical company Proximagen Group have formalized a partnership in which Lundbeck and Proximagen will jointly develop treatments for central-nervous-system disorders. Under the agreement, a steering committee of experts from both companies will focus on developing three of Proximagen’s programs with the aim of identifying therapies for epilepsy, pain, and inflammatory disorders. Lundbeck will also receive certain negotiation rights in relation to these programs and take a 9% stake in Proximagen for £10.3 million ($16.1 million).
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Silverson Ultra Sanitary In-Line high shear mixers are designed for facilities where clean-in-place (CIP), as well as sterilize-in-place (SIP) is required. Silverson is the only mixer manufacturer of its kind offering mixers certified to meet both 3-A Third Party Verification sanitary standards and the European Hygienic Engineering Design Group (EHEDG) standard considered the international benchmark for sanitation.
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Merck Serono, a division of Merck KGaA, signed two separate agreements with Ono Pharmaceutical, an R&D-oriented pharmaceutical company, for the treatment of multiple sclerosis (MS) and cancer. The first agreement grants Merck worldwide exclusive license rights for the development and commercialization of ONO-4641 [sphingosine-1-phosphate (S1P) receptor agonist] outside of Japan, Korea, and Taiwan, for the treatment of relapsing-remitting multiple sclerosis. The second license agreement provides Ono with codevelopment
and comarketing rights to Stimuvax (BLP25 liposome) in Japan for the treatment of nonsmall-cell lung cancer. Under the terms of the agreement for ONO-4641, Merck Serono will acquire worldwide exclusive rights, excluding Japan, Korea, and Taiwan, to develop and commercialize ONO-4641.
Ono will receive JPY 1.5 billion ($19.5 million) as an up-front payment and could receive additional payments based on the achievement of certain development, regulatory, and commercial milestones. Under the terms of the separate agreement, Ono will receive a codevelopment and comarketing license for Stimuvax in Japan, and Merck Serono will receive an upfront payment of EUR 5 million ($6.6 million).
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Roche has opened a new 17,000-ft2 clinical-supply manufacturing facility on its campus in Nutley, New Jersey. The Roche Center of Excellence produces dosage forms of highly potent compounds for preclinical safety studies and Phase I and II clinical studies. The clinical dosage forms produced at the facility include tablets, capsules, powders, suspensions, and solutions.
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CBI's 4th West Coast Forum on Clinical Supply Chain Management— December 6-7, 2011, Hyatt Regency San Francisco, Burlingame, CA Your link to Global Supply Chain excellence! Attend the premier west coast Clinical Supply Chain Management event of the year and hear regulatory guidance, operational efficiency and emerging technology perspectives from Eli Lilly, Genentech, Sanofi, Cerexa and more! Register by November 2nd at
www.cbinet.com/supplychainwest and save $400 with priority code: YSZ689 .
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Do you have news to report on facility expansions, contracts, service agreements, mergers, acquisitions, or personnel appointments? Send press releases to [email protected] |
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Roche has named Rainer Metternich as head of small-molecule research. He takes over from Klaus Strein, who will retire from Roche.
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