Biopharm Dev & Mfg Industry News

Pfenex Inc.’s Reagent Proteins division announced today that it has submitted a Biologics Master File (BMF) to the United States Food and Drug Administration for its cGMP grade CRM197 carrier protein to support the development of conjugate vaccine products by its partners.

Reagent Proteins is supplying cGMP grade CRM197 carrier protein to multiple partners in support of their novel conjugate vaccine development efforts. As part of the product offering partners are granted access to the BMF in support of regulatory submissions for their conjugate vaccines. The BMF was developed in partnership with Pfenex’s cGMP manufacturing partner, Serum Institute of India Ltd.

Serum Institute is a global leader in vaccine development and production whose vaccines have been used in over 140 countries around the world. It is estimated that two out of every three children immunized in the world is vaccinated by a vaccine manufactured by Serum Institute. The Pfenex CRM197 currently being manufactured at Serum Institute is also being used by Serum Institute as the carrier protein for its own internal Pneumococcal polysaccharide conjugatevaccine program.

“This filing with the US FDA marks another important milestone for our Reagent Proteins business unit,” said Dr. Bertrand Liang, CEO of Pfenex Inc, “The ability to provide our partners with access to high quality vaccine components produced using the powerful Pfenex Expression Technology™ as well as supporting their regulatory agency filings through providing access to Biologics Master Files, demonstrates our unique value proposition. By leveraging our long standing relationship with Serum Institute of India, we are able to provide our customers with a rapid and scalable path into the clinic and through to commercialization”

About Reagent Proteins
Reagent Proteins is a leading supplier of reagent, pre-clinical and cGMP grade proteins to the biopharmaceutical and vaccine development community. We ensure that scientists have ready access to a comprehensive offering of high quality proteins to enable their development efforts to proceed efficiently.

For more information please visit www.reagentproteins.com

About Pfenex Inc.
Pfenex Inc. is a protein production company leveraging the unique and powerful Pfenex Expression Technology™ platform based on the microorganism, Pseudomonas fluorescens, for the production of research proteins, reagent proteins, biosimilars and innovator biopharmaceuticals. For more information please visit www.pfenex.com

About Serum Institute of India Ltd.
Serum Institute of India Ltd. is the world's largest producer of Measles and DTP group of vaccines. It is estimated that two out of every three children immunized in the world is vaccinated by a vaccine manufactured by Serum Institute. Serum Institute of India was founded in 1966 with the aim of manufacturing life-saving immuno-biologicals, which were in shortage in the country and imported at high prices. Thereafter, several life-saving biologicals were manufactured at prices affordable to the common man and in abundance, with the result that the country was made self-sufficient for DTP (Diphtheria, Tetanus and Pertussis) group of Vaccines, MMR (Measles, Mumps and Rubella) group of vaccines and then later on Hepatitis B, HiB, Meningococcal A and combination vaccines.

About CRM197
CRM197 is a non-toxic mutant of diphtheria toxin having a single amino acid substitution of glutamic acid for glycine. CRM197 is a well defined protein and functions as a carrier for polysaccharides and haptens making them immunogenic. It is utilized as a carrier protein in a number of approved conjugate vaccines for diseases such as meningitis and pneumococcal bacterial infections. Pfenex CRM197 is a recombinant form expressed in Pseudomonas fluorescens using the Pfenex Expression Technology™ platform.


Pfēnex Inc., an industry leader in protein expression through the Pfēnex Expression Technology™ platform, announced today a three year strategic collaboration withMedImmune LLC, the global biologics business of AstraZeneca. The agreement provides MedImmune with non-exclusive access to Pfēnex Expression Technology and scientific resources for the development of bioprocesses for human therapeutic proteins and vaccines.

Pfēnex Inc. will engineer production strains and develop early production processes for MedImmune’s proprietary molecules. A Joint Steering Committee will be established to oversee the collaboration and facilitate the decision-making process. This collaboration provides MedImmune with access to an industry-leading expression platform and process development team that will enable preclinical and clinical development for these molecules to progress quickly and efficiently. MedImmune will provide annual technology access fees, FTE resource funding and will also have pre-agreed commercial license terms.

“This partnership with MedImmune will facilitate speed and reliability in the development of protein therapeutics and vaccines to serve unmet medical needs,” said Dr. Bertrand Liang, CEO of Pfēnex Inc. “Integrating our efforts early will allow for the rapid progression of early stage candidate molecules through discovery and development.”

“We are very excited to initiate this collaboration with Pfēnex” said Dr. Gail Wasserman, Senior Vice President of Biopharmaceutical Development at MedImmune. “Their scientific approach to strain development and protein expression is robust and aligned with the way we work at MedImmune. Working collaboratively with Pfēnex by harnessing their novel platform will play an important role in helping accelerate some of our early pipeline programs.”

About Pfēnex Inc.
Pfēnex Inc. is a protein production company leveraging the unique and powerful Pfēnex Expression Technology™ platform based on the microorganism, Pseudomonas fluorescens, for the production of research proteins, reagent proteins, biosimilars and innovator biopharmaceuticals. For more information please visit www.pfenex.com

About MedImmune, LLC
MedImmune, the global biologics unit for AstraZeneca PLC (LSE: AZN.L, NYSE: AZN), has approximately 3,500 employees worldwide and is headquartered in Gaithersburg, Maryland. For more information, visit MedImmune’s website at www.medimmune.com.


Pfenex Inc., announced today that Dr. George Klima, Head Process Science Microbial at Boehringer Ingelheim will present a Pfēnex Expression Technology case study at the 7th Annual PEGS Summit in Boston, MA. The presentation will focus on the expression of an antibody fragment.

In this presentation Dr. Klima will compare the production of a Fab fragment in Pfēnex Expression Technology with expression in E.coli (periplasmic), E. coli (inclusion body) and Pichia pastoris. The case study highlights the speed and production titer of each expression approach. The results show that Pfēnex delivered high titers of soluble, active protein with unprecedented speed and quality. Five hundred milligrams of 99% pure Fab fragment was delivered within ten weeks of receipt of gene. All three other expression approaches failed to produce any properly folded Fab.

In addition, Pfenex Inc. also announced that Russell Coleman, Molecular Biology Senior Scientist, will present a poster at the PEGS Summit on high throughput screening of cloning strategies and host strains to optimize antibody derivative expression.

“We are very pleased with both Dr. Klima’s presentation and Mr. Coleman’s poster,” Patrick Lucy, Vice President of Business Development explains. These presentations outline our unprecedented success rate, quality and the speed of our technology, and how we enable our customers avoid the opportunity costs associated with legacy expression hosts.”

Conference attendees are encouraged to attend Dr. Klima’s presentation scheduled for Tuesday, May 10, 2011 at 12:15 pm as part of the Difficult to Express Proteins Track. The conference will be held at the Sheraton in Boston, MA and will feature a select group of speakers from academia and industry.

For additional information please visit the Pfenex Inc. website.
Democratic and Republican party leaders and strategists will share their differing perspectives in a keynote panel, titled "The Future of Healthcare Reform," during a Keynote Luncheon at the 2011 BIO International Convention on June 29 at the Walter E. Washington Convention Center in Washington, DC.

Moderated by BIO's President and CEO Jim Greenwood, the panel will include U.S. Senator John Barrasso (R-WY), former U.S. Senator Tom Daschle, former Democratic National Committee Chair Howard Dean, and Republican political strategist Karl Rove. The panelists will discuss the challenges and opportunities associated with implementing "The Patient Protection and Affordable Care Act of 2009" as well as efforts to repeal and reform the law.

"This year's BIO International Convention in Washington, DC presents the ideal venue for debate and discussion among some of the greatest political and health care policy minds of our time on restructuring of the nation's healthcare system," said Greenwood. "It is critical for biotechnology leaders to be aware of the implications for the industry as the Obama Administration and Congress address healthcare reform implementation."

The Future of Healthcare Reform policy panel keynote will be sponsored by Amgen.

Prior to launching their political careers, Senator Barrasso and Governor Dean served as practicing physicians. Senator Daschle and Mr. Rove have been prominent voices on the healthcare debate and both are widely respected for their analysis of the issues presented on both sides.

The BIO International Convention is the largest global event for the biotechnology industry, offering networking and partnering opportunities with policymakers, scientists, CEOs and newsmakers, and hundreds of sessions covering biotech trends, policy issues and technological innovations. The 2011 BIO International Convention has a set of free search and event planning tools for media, attendees and prospective attendees. The myBIO tool allows easy search and access to the companies, attendees and events by topic.

The Convention features the BIO Business Forum for biotechnology and pharmaceutical companies, academic research institutions, and investors from around the world to gather and discuss strategic opportunities.

The BIO International Convention helps to support BIO programs and initiatives. BIO works throughout the year to create a policy environment that enables the industry to continue to fulfill its vision of bettering the world through biotechnology innovation. For more information on the global event for biotechnology, including program and housing information, please visit http://convention.bio.org/.

For registration, conference agenda and exhibitor information, visit http://convention.bio.org.

Members of the media can register at http://convention.bio.org/media.

Upcoming BIO Events

World Congress on Industrial Biotechnology & Bioprocessing
May 8-11, 2011
Toronto, Ontario, Canada

Partnering for Global Health Forum 2011
June 27, 2011
Washington, DC

BIO International Convention
June 27-30, 2011
Washington, DC

2011 BIO Human Resources Conference
June 26-28, 2011
Washington, DC

The Business Forum at the BIO International Convention
June 28-30, 2011
Washington, DC

BIO India International Partnering Conference
September 21-22, 2011
Hyderabad, India

BIO China International Conference
October 12-13, 2011
Shanghai, China

About BIO
BIO represents more than 1,100 biotechnology companies, academic institutions, state biotechnology centers and related organizations across the United States and in more than 30 other nations. BIO members are involved in the research and development of innovative healthcare, agricultural, industrial and environmental biotechnology products. BIO also produces the BIO International Convention, the world’s largest gathering of the biotechnology industry, along with industry-leading investor and partnering meetings held around the world. BIO produces BIOtechNOW, an online portal and monthly newsletter chronicling “innovations transforming our world.” Subscribe to BIOtechNOW.

For more information:
Visit http://www.bio.org

Follow us on Twitter @IAmBiotech

Join us on LinkedIn/MyBio

Become a fan at facebook.com/IAmBiotech

Finesse, LLC, Santa Clara, CA, a manufacturer of measurement and control solutions for life science process applications, has announced the official launch of three new core modules for advanced control in its fourth generation TruBio DV software. These modules are targeted at giving bioprocessing specialists the ability to utilize process data to create novel control strategies, facilitate sophisticated mathematical computation and logic based decision, and seamlessly utilizetheir own DeltaV control modules. Since its first launch in 2007, TruBio DV continues to be powered by a DeltaV Controller from Emerson Process Management, and is fully compatible with DeltaV versions 9.3 through 11.3.

“To date, TruBio DV software has integrated analog and OPC-based communication with a significant number of in-line and off-line sensors, thereby providing users with significant amounts of information about their process. Our new advanced control modules will allow users to actually use this information effectively for process characterization and optimization” stated Dr. Mark Selker, CTO at Finesse. He added, “TruBio DV 4.0 not only has significantly enhanced features for traditional sensor calibration, on-line DeltaV parameter access, and conditional alarming, but with the addition of these modules enables unique capability for both cell culture and fermentation applications.”

MathLogic provides an enhanced process parameter calculator as well as comparison and nested logic statement ability for rapidly optimizing process control campaigns. SmartDose is a new feature for liquid control that simplifies programming typical pump dosing algorithms such as bolus, ramp, and continuous feed, with or without feedback from weigh scales. BlackBoxControl unlocks TruBio for DeltaV automation experts by allowing them to program their own control modules for key process parameters such as pH, dissolved oxygen, and temperature, and then easily connect these custom modules to TruBio through a “parameter hook”.

“As we continue to increase the diversity of off-line instrumentation whose data we can easily mine, we expect to be able to build even more sophisticated process control strategies. This is similar to ourSmartDose software, where we expect a whole range of processing modules to be introduced this year” summarized Dr. Selker.

About Finesse Solutions, LLC
California-based Finesse Solutions, LLC, has established a proven record in providing turn-key, scalable solutions for single-use upstream bio-processing. The Finesse product platform includes an extensive portfolio of novel disposable sensors, modular configure-to-order automation hardware, and intelligent software that can harmonize global bio-process information and technology transfer. Finesse also offers a complete set of services including startup, commissioning, and validation for rapid and reliable deployment of single-use equipment into cGMP manufacturing applications. For more information, please visit us at www.finesse.com.

Finesse, LLC, Santa Clara, CA, a manufacturer of measurement and control solutions for life science process applications, has announced the official launch of two new core modules for off-line data processing in its fourth generation TruBio DV software. These modules are targeted at enabling bioprocessing specialists to manage data from third party equipment and process analyzers, and obtain automated electronic records of their batch. Since its first launch in 2007, TruBio DV continues to be powered by a DeltaV Controller from Emerson Process Management, and is fully compatible with DeltaV versions 9.3 through 11.3.

“TruBio DV software was originally developed to provide automation hardware independence and to utilize best in class components for upstream process management. TruBio DV 2.0 was optimized to enable easy scale-up and scale-down between R&D, process development, and cGMP manufacturing. TruBio DV 3.0 introduced OPC-based communication with third party analyzers such as the Nova BioProfile400 and FLEX back in 2008, and demonstrated automated feeding strategies and intelligent management of redundant process sensors for pH measurement” stated Basil Zimmo, VP of Software at Finesse.

RemoteView OPC allows seamless digital communication with third party process equipment and off-line process analyzers, so that TruBio DV can overlay on existing bioreactors to extend their useful life. BatchReport is an integrated electronic batch report generator that leverages all process data consolidated into the TruBio/DeltaV historian.

“To illustrate the power of TruBio DV 4.0 we look at existing examples: TruBio can overlay and direct over one hundred controllers from diverse manufacturers including Sartorius, Applikon, New Brunswick and DasGip, with customized cell-viabiity-based feed strategies using off-line measurements from a Nova FLEX, and simultaneously produce an electronic record comparing several bioreactors running in parallel for efficient design of experiment” summarized Mr. Zimmo.

About Finesse Solutions, LLC
California-based Finesse Solutions, LLC, has established a proven record in providing turn-key, scalable solutions for single-use upstream bio-processing. The Finesse product platform includes an extensive portfolio of novel disposable sensors, modular configure-to-order automation hardware, and intelligent software that can harmonize global bio-process information and technology transfer. Finesse also offers a complete set of services including startup, commissioning, and validation for rapid and reliable deployment of single-use equipment into cGMP manufacturing applications. For more information, please visit us at www.finesse.com.

Pfenex Inc., announced today that Jerry Ngai, Scientist, will be a featured speaker at the 241st American Chemical Society (ACS) Meeting & Exposition. Ngai’s presentation will detail the utility of the Pfenex Expression Technology™ platform to rapidly establish production processes for proteins that cannot be expressed in other host systems.

In recent years, development of vaccines has attracted increasing attention, with the launch of several blockbuster vaccines. Threats of pandemics and bioterrorism, and the need to reduce healthcare costs, has resulted in increased interest in this area from government agencies. Previous efforts in producing a significant number of vaccine antigens and carrier proteins have resulted in improperly folded or truncated protein. Pfenex Inc. has built an expression platform that directly deals with these challenges resulting in a robust technology that can rapidly and cost effectively produce vaccine components.

“Unlike platform processes commonly used for monoclonal antibody expression and purification, the diversity of vaccine antigens requires fermentation and purification processes tailored to each protein.” Ngai explains. “Pfēnex Expression TechnologyTM employs a toolbox of defined strains containing custom-designed combinations of genetic elements, including a broad array of protease-deficient strains to minimize proteolytic degradation; resulting in high level expression of a broad variety of vaccine antigens/carriers. Pfenex routinely leverages the platform to solve purification challenges which ultimately results in a more efficient and hence cost effective production process.” Ngai will be sharing the details regarding the Pfēnex Expression TechnologyTM approach as well as case studies at the ACS conference.

Conference attendees are encourage to attend the session scheduled for Wednesday, March 30, 2011 at 4:20pm as part of the Division of Biochemical Technology, down-stream processing track. The conference will be held at the Anaheim Convention Center in Anaheim, CA and will feature a select group of speakers from academia and industry. For additional information please visit the Pfenex Inc. website.

About Pfenex Inc.
Pfenex Inc. is a protein production company leveraging the unique and powerful Pfenex Expression Technology™ platform based on the microorganism, Pseudomonas fluorescens, for the production of research proteins, reagent proteins, biosimilars and innovator biopharmaceuticals. For more information, please visit www.pfenex.com

About the American Chemical Society Meeting & Exposition
With more than 163,000 members, the American Chemical Society (ACS) is the world’s largest scientific society and one of the world’s leading sources of authoritative scientific information. A nonprofit organization, chartered by Congress, ACS is at the forefront of the evolving worldwide chemical enterprise and the premier professional home for chemists, chemical engineers and related professions around the globe.

Biochemical Technology (BIOT) is a division of the American Chemical Society. The mission of the division is to promote the exchange of information among academic and industrial researchers regarding technology utilizing life-based systems to produce useful products and services.

The 241st ACS National Meeting & Exposition is being held at the Anaheim Convention, March 27-31.
Finesse Solutions, LLC, a manufacturer of measurement and control solutions for life sciences process applications, announced a live demonstration of its new SmartBagproduct for rocker bioreactors at Interphex 2011 in New York, March 29-31.

Bioprocessing specialists will get aclose-up look at the first robustsingle-use of theSensorPaksolution that has been seamlessly integrated into a pillow bag and is resistant to gamma radiation sterilization. SmartBags are designed to be plug-and-play bio-processingcontainers having full measurement capability for at least 21 days.

The SmartBagSensorPak leverages TruFluor pH and dissolved oxygen phase fluorometrictechnologyin a compact assembly that is pre-calibrated using a SmartChip and provides accurate, drift-free, in-situ measurements. The combined pH and DO optical reader uses advanced optical components including a large area photodiode that minimizes photo-degradation of the active sensing elements. The SensorPak also leverages TruFluor temperature 316L stainless steel thermal window for highly stable readings. The SensorPak is welded into the single-use vessel and eliminates the need for sterile connectors and their associated complications such as leakage and batch contamination. All wetted materials of the SensorPak are USP class VI compliant and being identical to TruFluor, allow directly measurement comparisons and scale-up from 10L rocker bags to 2,000L SUBs.

A SmartBag retrofit for the most commonly utilized rocker platform trays will be demonstrated at the show, along with the T300 labscale controller for gas and liquid management. According to Finesse Solutions CTO Dr. Mark Selker, “It is a pleasure to introduceSmartPak technology and the Smartbag to the bioprocessing market at such a major event. This product is optimized for accuracy, lifetime, and ease of use. We anticipate that the SensorPakwill provide a unique, complete solution for single-use seed train bio-processing applications, which are still in great need of reliable and trustworthy key process parameter measurements.”

About Finesse Solutions, LLC
California-based Finesse Solutions, LLC, has established a proven record in providing turn-key, scalable solutions for single-use upstream bio-processing. The Finesse product platform includes an extensive portfolio of novel disposable sensors, modular configure-to-order automation hardware, and intelligent software that can harmonize global bio-process information and technology transfer. Finesse also offers a complete set of services including startup, commissioning, and validation for rapid and reliable deployment of single-use equipment into cGMP manufacturing applications. For more information, please visit us at www.finesse.com.

Hosted Solution will Improve Patient Outcomes, Research and Collaboration by Integrating Clinical and Molecular Data from Three Major National Health Service Trusts and Leading University

Guildford, UK, and Burlington, Mass., March 9, 2011 - IDBS, a global provider of innovative data management, analytics and modeling solutions, today announced that it will provide a unique, enterprise translational medicine platform for the Integrated Cancer Centre at King’s Health Partners. The Oncology Research Information System, (ORIS), designed at the Integrated Cancer Centre and developed and delivered by IDBS, will enable King’s Health Partners to develop targeted, personalized, cancer therapies according to the specific genetic and other characteristics of individual patients. This will improve the likelihood and number of successful treatment outcomes.

ORIS is the first of its kind: a single cross-organizational research platform that will bring together patient data for all King’s Health Partner’s cancer cases, accounting for a quarter of hospital beds in London. This comprehensive approach to cancer research has never before been able to be handled in one IT platform. ORIS will provide a unique translational medicine hub, handling the complex analytical demands of translational research and improving collaboration between the partners - King’s College London University, King’s College Hospital, Guy’s and St Thomas’ and South London and the Maudsley NHS Foundation Trusts.

IDBS, through the ORIS platform and associated organizational changes, will provide King’s Health Partners with:

  • improved cancer treatment through secure knowledge sharing of patient outcome information;
  • one secure searchable hub for clinical, diagnostic, pathological, sample, research and genomics centric information integrated from multiple sources;
  • highly secure information governance and pseudonymization procedures to protect patient confidentiality;
  • comprehensive scientific and statistical analytics to support requirements across research, teaching and clinical needs;
  • reduced complexity with high security through scalable, flexible hosting and rigorous access control;
  • powerful visualization of translational research data and an evaluation of data quality;
  • an enhanced competitive position for attracting pharmaceutical and other research partners.

“Despite all the progress medical science has made, many cancer patients are still treated with protocols identified through a process of trial and error. Our aim is to change this through a targeted approach to cancer therapy, which will improve outcomes and patient quality of life,” said Professor Peter Parker, PhD, FRS, Head of the Division of Cancer Studies and R&D Lead for the Integrated Cancer Centre at King’s Health Partners. “Critical to this effort is a new collaboration between the different research and healthcare organizations involved and, above all, access to relevant data and analytics to enable our multi-disciplinary research teams to deliver outcome-based therapies.”

“During our extensive competitive tender process, IDBS clearly demonstrated a unique understanding of the complexities of translational medicine, core software provision and solution integration that we required for this program,” continued Professor Parker.

“IDBS understands that the improvement of patient outcomes will come from the successful delivery of targeted treatments, which requires a fundamental change in the approach healthcare organizations take to using increasingly complex research information and sharing of the clinical knowledge they generate,” said Neil Kipling, founder and CEO of IDBS. “Our broad understanding of the healthcare and pharmaceutical research sectors enables us to deliver the enabling technologies required to make the promise of personalized medicine a reality. The ORIS project further validates our strategy to design and build enterprise data management and analytics systems targeted at improving healthcare provision in the UK and worldwide.”

This is the first step in a five-year strategic relationship that could eventually expand to cover all disease areas including all oncology disorders and cardiovascular disease.

About King’s Health Partners
King’s Health Partners Academic Health Sciences Centre (AHSC) is a pioneering collaboration between King’s College London, and Guy’s and St Thomas’, King’s College Hospital and South London and Maudsley NHS Foundation Trusts

King’s Health Partners is one of only five AHSCs in the UK and brings together an unrivalled range and depth of clinical and research expertise, spanning both physical and mental health. Our combined strengths will drive improvements in care for patients, allowing them to benefit from breakthroughs in medical science and receive leading edge treatment at the earliest possible opportunity.

For more information, visit www.kingshealthpartners.org

About IDBS
IDBS is a global provider of innovative enterprise data management, analytics and modeling solutions. The company’s uniquely sophisticated platform technologies are used by more than 200 pharmaceutical companies, major healthcare providers, global leaders in academic study, and high tech companies to increase efficiency, reduce costs and improve the productivity of industrial R&D and clinical research. IDBS is clearly differentiated by its unique combination of award-winning enterprise technologies and domain knowledge in R&D.

IDBS’ solutions help scientists, hospitals and R&D businesses produce the world’s newest therapeutics, diagnostics and personalized treatments, high-tech materials and consumer products, faster, cleaner engines and fuels, breakthroughs in productive agriculture, healthy, safer food products, and high tech materials and products.

Founded in 1989 and privately held, IDBS is headquartered in Guildford, UK with a direct sales and support presence worldwide. IDBS is a Profit Track 100 company and the recipient of multiple awards including the Frost and Sullivan ‘Enabling Technology’ Award in R&D data management for 2010. For regular updates follow us on Twitter @IDBSsoftware.

www.idbs.com
SciLog, Inc. announces the issuance of the second of two single-use sensor patents, US 7,788,047 and US 7,857,506 “Disposable, Pre-Calibrated, Pre-Validated Sensors for Use in Bio-Processing Applications.” The first patent was issued in September 2010.

“This patented technology addresses the challenges of the Process Analytical Technology (PAT) initiative as it applies to single-use sensors in downstream bio-processing” commented Karl G. Schick, Ph.D., VP of R&D at SciLog Inc.

SciLog’s single-use, pre-calibrated sensors:  Provide real-time analytical data. Enable pre-sterilized, closed-loop processing environments. Can be integrated into single-use, gamma-irradiated fluid pathways (SciLog US patents 6,712,963 and US 7,052,603), enable automation and automated data acquisition for single-use platforms.

SciLog manufactures disposable, pre-calibrated, single-use conductivity (SciCon), pressure (SciPres) and temperature (SciTemp) sensors. The sensors are designed with process scalability in mind. They are available in five different fluid connection sizes, ranging from Luer (Laboratory) to 1.0” TC (GMP bio-processing), are available in each of the sensor families. Each sensor is NIST traceable by sensor ID and comes with a calibration certificate and appropriate compliance statements. Sensor ID and associated calibration data are stored in a gamma-stable memory residing within the sensor. The stored calibration data is stable for over two years. For more information, go to www.scilog.com/sensors.

These patents expand SciLog’s patent position in downstream, single-use technology. In addition to the newly issued sensor patents, SciLog has received two prior patents (US Patent 6,712,963 and 7,052,603) that deal with “Single-use Manifolds for Automated, Aseptic Transfer of Solutions in Bio-Processing Applications”. SciLog has also received US Patent 7,410,587 for “Liquid Handling for Filtration and Liquid Chromatography”. Specifically, these patents address the challenges and provide solutions relevant to downstream, single-use purification by tangential flow filtration (TFF), preparative chromatography and normal flow filtration (NFF).

SciLog offers licensing arrangements of its single-use technology to interested parties.
Page 4 of 5

Want more? Visit...

Videos

  • ICON- Partnerships 12
    ICON- Partnerships 12 Steven Cutler, Group President of ICON discusses the launch of ICON's new acquisition of Firecrest at Partnerships in Clinical Trials 2012. Facing the continuing challenge of not only monitoring and…
    Read more...
  • ICON- Partnerships 12
    ICON- Partnerships 12 Steven Cutler, Group President of ICON discusses their exciting new partnership with Roche at Partnerships In Clinical Trials 2012. Medical imaging has always been a strong department within ICON. ICON…
    Read more...
  • ERT- Partnerships 12
    ERT- Partnerships 12 John Blakely, Executive Vice President and Chief Commercial Officer for ERT discusses the new trend in clinical research at Partnerships in Clinical Trials 2012 - the melding of objective and…
    Read more...
  • Chiltern- Partnerships 12
    Chiltern- Partnerships 12 Marcelo Piccirillo, Senior Clinical Research Physician for Chiltern, discusses new trends in gastrointestinal clinical development at Partnerships in Clinical Trials 2012. Current hot spots for clinical development in the field…
    Read more...
  • Blinded Diagnostics - Partnerships 12
    Blinded Diagnostics - Partnerships 12 Paul Savuto, President and CFO, and Steven Karrupan, CEO, from Blinded Diagnostics discuss Point of Care Technology at Partnerships in Clinical Trials 2012. Point of care (or decentralized testing) offers…
    Read more...
  • American Airlines - IQPC 2011
    American Airlines - IQPC 2011 American Airlines has globally launched a passive solutions that gives a new alternative to pharmaceutical manufacturers.
    Read more...

Podcasts