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Podcasts

Webcast: A Unique Workflow for Linearity Using Automated Sample Preparation and UHPLC
Jan. 20, 2011—Sponsored by Dionex & Mettler-Toledo

Webcast: Risk Management for Pharmaceutical Manufacturing and Equipment: Meeting Regulatory Expectations and Preventing Contamination
Jan. 27, 2011—Sponsored by Alfa Laval

Webcast: Solubilization and Stability of Drug Actives
On-Demand—Sponsored by Croda

Webcast: Protect IP and Reduce the "Sign and Witness" Burden in Lab Informatics Systems
On-Demand—Sponsored by Surety

Webcast: Topical Drug Product Development: Overcoming CMC Issues and Pitfalls- Analytical & Regulatory
On-Demand—Sponsored by Dow Pharmaceutical Sciences

Podcast: Interviews with AAPS 2010 Science Award Winners

Podcast: Thomas Otto on Vetter Secondary Packaging

Podcast: Lou Schmukler on Pfizer's Manufacturing Strategy

Podcast: Joseph Forth of AMRI on Clinical Formulations

Events

Pharmacovigilance and Risk Management 2011
Jan. 9–12
Washington, DC

Life Sciences Serialization & Traceability for Brand Protection
Jan. 24–25
Philadelphia

Biomanufacturing Summit 2011
Jan. 24–25
San Diego

Cool Chain Europe 2011
Jan. 24–26
Rotterdam, The Netherlands

Social Media in the Pharmaceutical Industry
Jan. 26–27
London

Process Validation for Drugs and Biologics
Jan. 27–28
King of Prussia, PA

InformexUSA 2011
Feb. 7–11
Charlotte, NC

Pharma Test Expo 2011
Feb. 8–10
Cologne, Germany

More events


FindPharma Search
December 30, 2010 PharmTech.com

News

FDA to Officially Join PIC/S
After five years of discussions, the US Food and Drug Administration is joining the Pharmaceutical Inspection Convention and the Pharmaceutical Inspection Cooperation Scheme as of Jan. 1, 2011.
Click Here to Read More

EMA Outlines Work Program for 2011 and Adopts New Five-Year Plan
The European Medicines Agency outlined its work program and budget for 2011. Click Here to Read More

Dr. Reddy's Forms Technology and Manufacturing Pact in Russia
Dr. Reddy’s Laboratories has entered into a technology transfer, manufacturing, and marketing agreement with R-Pharm, a Russian pharmaceutical company. Click Here to Read More



Product Spotlight

Overmolded fittings reduce entrapment

AdvantaPure’s (Southampton, PA) Overmolded Tri-Clamp Ends are suitable for applications such as transferring media, dispensing, and final filling. Because polypropylene fittings are thermally mated to the end of the tubing, the overmolded products provide a completely smooth inner diameter that reduces the opportunity for bacterial entrapment, compared with barb-type fittings. The overmolded fittings also eliminate leakage and minimize the risk of contamination because they do not rely on mechanical connections.

The Overmolded Tri-Clamp fittings are available for various sizes of polyvinyl chloride, thermoplastic elastomer, and thermoplastic rubber tubing. The fittings do not restrict flow or the inner diameter of the tubing. Clients can choose fitting models that are injection molded from US Pharmacopoeia Class VI thermoplastic polyester elastomers or polypropylene. The Tri-Clamp Ends are certified free of animal-derived ingredients and are designed to be cleaned and sterilized easily. In addition, AdvantaPure can provide molded silicone assemblies and various single-use process components.

Company Notes

Abbott Diabetes Care (Alameda, CA) is working with the US Food and Drug Administration to recall 359 different lots of glucose test strips marketed under the following brand names: Precision Xceed Pro; Precision Xtra; Medisense Optium; Optium; OptiumEZ; and ReliOn Ultima. These strips are used with Abbott’s Precision Xtra, Precision Xceed Pro, MediSense Optium, Optium, Optium EZ, and ReliOn Ultima blood-glucose-monitoring systems. As many as 359 million strips may be affected by the recall, according to an FDA press release. The agency stressed that blood-glucose-monitoring systems are not affected by this recall.

Advertisement:
Contract Manufacturing and Packaging for Solid Oral Dosage

Ropack, a leader in packaging solutions for the pharmaceutical, biopharmaceutical and nutraceutical industries, now provides the technology and expertise for stickpack packaging of solid oral dosage in a low relative humidity and temperature-controlled environment. Stickpacks – slim, tube-shaped packets the size of a stick of gum – offer impressive benefits: fill accuracy, portability, product differentiation, reduction in paper and foil usage, product differentiation and ideal sample option. http://www.ropack.com/en/service/primary-packaging/stick-pack

AstraZeneca (London) and Abbott (Abbott Park, IL) ended their development program for Certriad (rosuvastatin calcium and fenofibric acid), a potential treatment for mixed dyslipidemia. The companies received a Complete Response Letter (CRL) from FDA for the drug’s new drug application in March 2010 and have decided to end the program after evaluation of the CRL, according to a company statement.

Biopharmaceutical company Cephalon (Frazer, PA) decided to stop development of Nuvigil (armodafinil) tablets [C-IV] for the treatment excessive sleepiness associated with jet-lag disorder. The company received a second CRL from FDA that reiterated the agency’s previously stated concerns about the drug.

Advertisement:
Interphex

Thousands of pharmaceutical, biologic, generic, and contract services professionals gather annually at INTERPHEX (March 29-31, 2011, Javits Convention Center, New York City) to see new products, network, and learn about emerging trends surrounding drug manufacturing. At INTERPHEX 2011, you’ll find the solutions and education you need to ensure quality, improve efficiency, and solve your manufacturing and supply chain problems. Register for a free exhibit hall pass at www.INTERPHEX.com

Cepheid (Sunnyvale, CA), a molecular diagnostics company, released Xpert Flu diagnostic test in Europe. The test, which runs on the company’s GeneXpert system, simultaneously detects and differentiates Flu A, Flu B, and 2009 H1N1 influenza virus in about one hour. The test was released as a European CE IVD Mark product under the European Directive on In Vitro Diagnostic Medical Devices. Since the beginning of the 2010-11 flu season, Europe has seen a resurgence of the 2009 H1N1 virus, according to a company press release.

Dey Pharma (Basking Ridge, NJ), a subsidiary of Mylan (Canonsburg, PA), will partner with Meda (Solna, Sweden) a specialty pharma company, for the exclusive marketing and distribution rights of EpiPen (epinephrine) Auto-Injector in Europe. EpiPen Auto-Injector is used for emergency treatment of severe allergic reactions (anaphylaxis).

Advertisement:
Enercon
On-Demand Webinar & Whitepaper: Achieve a Perfect Seal
Get exclusive access to this on-demand webinar and whitepaper to learn the basic principles of the induction sealing process. Enercon Industries and Selig Sealing Products team up to discuss the three critical elements required to achieve a perfect seal, remedies for common application issues and techniques used to maximize line efficiencies.
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EpiTherapeutics (Copenhagen) and Abbott (Abbott Park, IL) formed a three-year agreement to develop anticancer drugs by making small-molecule inhibitors against selected epigenetic oncology targets. EpiTherapeutics will receive an upfront payment, funding for its research activities, and possible milestone payments and royalties. Additional financial details were not disclosed.

Merrion Pharmaceuticals (Dublin), a product development company, signed a pact with Novo Nordisk (Bagsværd, Denmark) to evaluate the ability of Merrion's proprietary Gipet drug-delivery technology to boost the oral bioavailability of an undisclosed proprietary compound. Following the feasibility studies, Novo Nordisk will have the option to enter into a further licensing agreement for the Gipet technology. Under the agreement, Merrion has granted Novo Nordisk a 20-day warrant to acquire up to EUR 1.5 million ($1.97 million) in ordinary shares at EUR 2.73 ($3.58) per share. In addition, Merrion can request Novo Nordisk to acquire up to EUR 500,000 ($656,000) worth of shares. The companies have license agreements for oral GLP-1 and insulin.

Mylan (Canonsburg, PA) agreed to pay $65 million to settle pricing lawsuits brought against it on behalf of the federal government and the state of Texas pertaining to Medicaid reimbursements paid by the federal government and the state of Texas to pharmacists and other healthcare providers. The settlement reflects the finalization of an agreement made in principle among the parties early in 2010 and reported in the company's 2009 Form 10-K. According to a company statement, the settlement agreement confirms that the resolution of the cases does not constitute an admission, finding, or evidence of fault, liability, or wrongdoing by Mylan.

Biopharmaceutical company Transition Therapeutics (Toronto) and Elan (Dublin), a biotechnology company, agreed to modify their collaboration agreement for the development and commercialization of ELND005 (scyllo-inositol), an investigational treatment for Alzheimer's disease. Under the terms of the modification, in lieu of a contractually required Phase III milestone payment, Transition will receive a payment of $9 million at the time of signing and will be eligible to receive a $11 million payment at the start of the next ELND005 clinical trial. Transition also will be eligible to receive up to $93 million in additional regulatory and commercial launch-related milestone payments plus tiered royalties ranging from 8% to 15% based on net sales of ELND005. Transition will no longer fund the development or commercialization of ELND005 and will relinquish its 30% ownership of ELND005 to Elan.

VAC-U-MAX (Belleville, NJ), a provider of pneumatic conveying systems and industrial vacuum cleaners, moved into its new 71,000-ft2 facility that houses the company’s assembly, fabrication, inventory, and corporate offices. The new facility also includes a 6000-ft2 test and demonstration facility that can simulate conditions at a customer’s site.

Do you have news to report on facility expansions, contracts, service agreements, mergers, acquisitions, or personnel appointments? Send press releases to ptpress@advanstar.com

People Notes

Cephalon (Frazer, PA) appointed J. Kevin Buchi as CEO and a member of the board of directors. Former Founder, Chairman, and CEO Frank Baldino, Jr. passed away earlier this month. The company said its board will address the role of company chairman in the future. William P. Egan will continue to serve as Cephalon's independent presiding director.

Lonza (Basel) appointed Harry Boot as the new COO for its Life Science Ingredients sector and as a member of the Lonza Management Committee, effective Mar.1, 2011. He takes over the position from CEO Stefan Borgas, who headed the sector on an interim bases since June 2010.

eResearchTechnology (ERT, Philadelphia), a global provider of technology and services, confirmed that the effective date of the previously announced retirement of President and CEO Michael J. McKelvey was Dec. 21, 2010. Joel Morganroth, currently ERT's chairman and chief scientific officer, will serve as interim president and CEO until the company hires a permanent replacement.

Lotus Pharmaceuticals (Beijing), appointed four new members of its board of directors following the resignation of four board members. Michael Toups, Lijun Fan, Zhaohui Li, and Jun Lu have been appointed to serve on the company's board of directors. They will replace current directors Li Ping, Liu Jin, Xian Xuemei, and Song Zhenghong.

The Pharmaceutical Research and Manufacturers of America (PhRMA) elected the following four new members to its board of directors: Ian Read, president and CEO of Pfizer (New York); Jerzy Gruhn, president of Novo Nordisk (Bagsværd, Denmark); Mark Iwicki, president and CEO of Sunovion Pharmaceuticals (Marlborough, MA); and Staffan Schuberg, president Lundbeck (Copenhagen).

US Oncology (The Woodlands, TX), an integrated oncology company, named Karen Gibson senior vice-president and chief information officer.

PharmTech, the magazine
Current Issue cover
Take the 8th Annual Global BioManufacturing Survey
Budget trends, new technologies, capacity, outsourcing and hiring issues, downstream processing, disposables, cost cutting, and quality initiatives, are just a few of the important topics covered in this year's 8th Annual Biopharmaceutical Manufacturing Report and Survey held by BioPlan Associates, Inc. Last year, more than 400 biomanufacturers and suppliers participated globally, and this year we're expecting even more. You will receive a free summary of the results from the study. In addition, for each completed survey, BioPlan Associates will donate $10 (up to $10,000) to the Global Alliance for Vaccine Initiative, or American Cancer Society.
Click Here to Read More

Coming Soon: A peer-reviewed article features a comparison of extrusion systems in the January issue of Pharmaceutical Technology.

 

 
 
 
 
 

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