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World Generic Medicines Congress Europe 2012
February 28, 2012—March 2, 2012
London, United Kingdom
Fundamentals of Lyophilization
March 12, 2012—March 13, 2012
Bethesda, Maryland, USA
Encouraging Development of Therapeutics for Neglected Diseases
March 12, 2012—March 13, 2012
Philadelphia, Pennsylvania, USA
DCAT Week
March 12, 2012—March 15, 2012
New York, New York, USA
Parenteral Packaging
March 13, 2012—March 15, 2012
Berlin, Germany 
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FDA Issues Warning Letters for Three Merck KGaA Plants
On Feb. 21, 2011, FDA posted a copy of a Warning Letter that was sent to the chairman of the executive board of Merck KGaA on Dec. 15, 2011, regarding cGMP violations identified at three of its European facilities: MS-Corsier-sur-Vevey, MS-Aubonne, and MS-Tiburtina. 
Pfizer, Zhejiang Hisun Pharmaceuticals Sign Generic-Drug Deal
Pfizer has signed an agreement with the Chinese biopharmaceutical company Zhejiang Hisun Pharmaceuticals with the objective of establishing a $545-million joint venture to develop and commercialize branded generic medicines in both China and the global market. 
McNeil Voluntarily Recalls Infants' Tylenol Oral Suspension Product
On Feb. 17, 2012, McNeil Consumer Healthcare, a division of McNeil-PPC, a subsidiary of Johnson & Johnson, voluntarily recalled approximately 574,000 bottles of its OTC pain reliever and fever reducer Infants' Tylenol Oral Suspension, 1 oz. Grape. The voluntary recall was initiated after consumers complained of having difficulty using the SimpleMeasure dosing system. 
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Power monitors provide insight into energy use
Endress+Hauser introduced an Installed Base Audit program to improve management of process instrumentation. Endress+Hauser works with plant maintenance personnel to input process measurement device information into a W@M Life Cycle Management database, and recommends preventive and corrective maintenance of devices. The database enhances traceability and management of all installed measurement devices. For example, the database helps users make sure replacement parts are available for each critical device, but eliminate unnecessary spare parts to reduce stock. Users can also access measurement device documentation through the database. Software tools allow users to control and document maintenance and calibration work. |
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Bedford Laboratories has announced a nationwide voluntary recall for the following three lots of Cytarabine for injection, USP: Cytarabine (cytarabine) for Injection (for treating leukemia), USP 1 g per vial, NDC #55390-133-01 lot 2066986 (expiration (exp.) date Mar. 31, 2014), lot 2111675 (exp. date: Apr. 30, 2014), lot 2131148 (exp. date: May 31, 2014).
The voluntary market recall is being conducted due to a postrelease investigation of the manufacturing area which determined a potential elevated risk of a lack of sterility assurance for these specific lots.
To date, there have been no reports of any adverse events for the lots being recalled, according to the company. Initial recall notification of the Cytarabine for Injection lots listed above were sent to impacted wholesalers and distributors by overnight courier and arranged for return of all recalled product. Hospitals, emergency rooms, clinics, physician offices, and other healthcare facilities and providers should not use the product lots listed above for patient care and should immediately quarantine any product for return. Read More
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Pharmaceutical starches from Grain Processing Corporation (GPC) range from basic unmodified starches for tableting to very specialized, innovative starches for unique applications. Spress® Pregelatinized Corn Starches NF perform as binders, disintegrants and lubricants for granulations, direct-compression tablets, capsules, dry blends and roller compaction. PURE-COTE® film-forming starches are designed for coating applications, oral thin films, capsules and any applications where clear, flexible films are required. Read More |
Biogen Idec has agreed to acquire Stromedix, a biotechnology company focused on therapies for fibrosis and organ failure. Under the terms of the agreement, Biogen Idec will make an upfront cash payment of $75 million and additional contingent value payments of up to $487.5 million based on the achievement of certain development and approval milestones across multiple indications. Stromedix's lead candidate, STX-100, for treating fibrotic disease, is a humanized monoclonal antibody that selectively disrupts the TGF–beta pathway. Read More
The United Kingdom's (UK) Medicines and Healthcare products Regulatory Agency (MHRA) has suspended the license of levothyroxine 100-microgram (mcg) tablets (levothyroxine sodium), manufactured by Teva, for treating hypothyroidism. This follows manufacturing difficulties and concerns that the product might not be interchangeable with other available levothyroxine 100-mcg tablets. This may lead to a loss of control of hypothyroidism when switching between products. Only levothyroxine 100-mcg tablets supplied in the Teva and Numark brands are affected. As this medicine is a generic drug, alternative products are available and most patients are unlikely to notice any change if they are switched from the Teva product to another levothyroxine product.
Teva levothyroxine 100-mcg tablets will cease to be available in the UK within the next few weeks as stocks are exhausted. The decision to suspend follows a review by the Commission on Human Medicines (CHM), the MHRA's independent advisory body, of manufacturing issues and sporadic reports of loss of control of hypothyroidism when switching between products. As a precautionary measure, while investigations are pending, Teva has voluntarily ceased manufacture and distribution in line with the CHM recommendation. The CHM review concluded that it may not be possible to switch use of the Teva product with other levothyroxine products, and that no further supplies of the product should be released for marketing until the aforementioned issues are resolved. Read More
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Podcast - Process Validation for Sterile Manufacturing
Join William (JR) Humbert, the Validation Manager at Cook Pharmica, as he discusses the 2011 FDA Guidance for the Industry, Process Validation: General Principles and Practices, and the impact the guidance has for biotechnology and pharmaceutical companies performing sterile manufacturing process validation. |
Merck & Co. has formed a joint venture (JV) with Supera Farma Laboratorios, a Brazilian pharmaceutical company co-owned by Cristália and Eurofarma. The new JV will market, distribute, and sell a portfolio of pharmaceutical and branded generic-drug products from Merck, Cristália, and Eurofarma solely in the Brazilian retail sector. Read More
Mylan and Pfizer have announced that Meridian Medical Technologies, a Pfizer subsidiary, has entered into a settlement agreement with Intelliject and Sanofi that will resolve pending patent litigation related to Intelliject's 505(b)(2) new drug application for its epinephrine autoinjector known as e-cue, which will be manufactured and marketed by Sanofi. According to the terms of the settlement, Intelliject and Sanofi may launch e-cue no earlier than Nov. 15, 2012, subject to receipt of final approval from FDA. Read More
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Handheld Raman Accelerates Raw Material Release
Enwave Optronics introduces the NEW ASSUPx Handheld Raman Analyzer for raw material verification. Most materials are measured and evaluated within 15 seconds. The ASSPx is fully 21 CFR Part 11 compliant for GMP requirements. It is an ideal choice for pharmaceutical, industrial chemicals and applications requiring high speed, reliable Raman analysis.
Enwave Optronics, Inc.
http://www.enwaveopt.com/EZRaman-H.htm
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Industry Briefs:
A roundup of additional company and people news from pharmaceutical and biopharmaceutical companies, their suppliers, and contract-service providers. Read More
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Overcoming Challenges in Complex Formulation Development: Bilayer Tablets & Beads-in-Capsules
LIVE WEBCAST: Tuesday, April 3, 2012 at 11:00 am EDT
Choosing the right formulation for a molecule is a challenging process. Whether you are looking to extend the life cycle of a drug or handling complicated APIs, there are multiple formulation options available for solid dose forms.
Register free at http://www.pharmtech.com/bilayer |
Do you have news to report on facility expansions, contracts, service agreements, mergers, acquisitions, or personnel appointments? Send press releases to ptpress@advanstar.com |
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