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Press release news from the public relations clients of Tiziani Whitmyre, Inc.

Manufacturing Newsfeed


Monday, January 23rd, 2012

Disinfectant Qualifications in Pharmaceutical Manufacturing Environments is Focus of New White Paper

AGAWAM, Mass. — Jan. 23, 2012 — A new white paper outlining the six steps that pharmaceutical and medical device manufacturers must employ to qualify disinfectants used in their environmental cleaning processes is now available from Microtest Laboratories athttp://www.microtestlabs.com/6stepspaper-disinfectant-qualification.

“Sterile pharmaceutical and medical device manufacturing environments require an effective cleaning and disinfection program to maintain aseptic conditions and prevent the microbial contamination of the product. The qualification of the chemical disinfectants used in these environments is extremely important, yet it is often overlooked,” stated Deborah Ensign, supervisor, R&D of Microtest Laboratories, in the new white paper, “Six Steps to Qualifying Disinfectants.”

In fact, “disinfectant qualifications require more planning, time, and resources than many companies realize,” she said.

“Any time a new disinfectant is introduced into the cleaning process within the facility, a qualification should be performed. From start to finish, a disinfectant qualification can require from 2 to 12 months.

“The timeline for a disinfectant qualification will depend on a number of variables, including the number of disinfectants and challenge organisms being tested as well as the number of surfaces (for the coupon method) being evaluated,” Ensign noted.

“The bottom line is that no matter whether the disinfectant qualification is performed internally — or by an outside testing laboratory — these six steps must be addressed,” she warned.

Download a free copy of the white paper, “Six Steps to Qualifying Disinfectants” for pharmaceutical manufacturing companies from Microtest Laboratories website athttp://www.microtestlabs.com/6stepspaper-disinfectant-qualification.

Deborah Ensign is supervisor, R&D Lab, at Microtest Laboratories Inc. She has over 20 years of experience in regulatory microbiology and contract laboratory operations. Ms. Ensign supervises Microtest’s Specialized Microbiology department. She holds a bachelor of arts degree in microbiology and is a nationally registered microbiologist. Ms. Ensign oversees all reusable testing (cleaning, disinfecting, and sterilization) and serves as a resource for USP testing, specifically <51>, <61>, and <62>.

About Microtest Laboratories
Microtest Laboratories is a leader in testing services and contract manufacturing for the medical device, pharmaceutical manufacturing, and biotechnology industries. Based in Agawam, Massachusetts, U.S.A., the company provides expertise and flexible processes that enhance product safety and security, accelerate time to market, and minimize supply chain disruption. For more information, visithttp://www.microtestlabs.com or call 1-413-786-1680 or toll-free 1-800-631-1680. Follow Microtest Laboratories on Twitter@MicrotestLabs at http://twitter.com/MicrotestLabs.

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Monday, September 26th, 2011

Fluid Automation: Unsung Contributor to Plant Economic Performance — New Management Brief from ASCO Numatics

FLORHAM PARK, N.J. — Sept. 26, 2011 — While fluid automation products — valves, pneumatics actuators, and similar components — control the flow of a process liquid or a supply of compressed air, they can also help control the flow of profits, according to a new management brief from ASCO Numatics.  Titled “Fluid Automation: The Unsung Contributor to Plant Economic Performance,” the brief is available for download at http://goo.gl/9MMkH.

The speed and reliability of fluid control products can provide competitive economic advantages in industrial operations worldwide. This is due to their ability to extend overall equipment service life, reduce warranty costs, cut maintenance/repair/operations (MRO) inventories, and increase production uptime and productivity.

But the choice of fluid automation technology is critical. For end users, judicious selection of fluid automation components must play a key role in their performance improvement plans. For original equipment manufacturers (OEMs), the right fluid automation choices provide significant cost, time-to-market, and product competitive advantages.

The new management brief examines available solutions and discusses how they  have maximized both speed and reliability — and provided surprisingly strong contributions to the economic performance of industrial operations.

The contents of the brief include:

  • Changing the Rhythm
  • Feeding the Bottom Line
  • The Benefits of Reliability
  • The Power of Speeds
  • Advantages for the OEM
  • Advances for the End User

Download the new management brief, “Fluid Automation: The Unsung Contributor to Plant Economic Performance,” from http://goo.gl/9MMkH.

Follow ASCO Valve on Twitter at http://twitter.com/ascovalve and on Facebook at http://www.facebook.com/ascovalve.

About ASCO Numatics

ASCO Numatics, a division of Emerson, offers comprehensive fluid automation solutions, including fluid control and fluid power products, for a wide range of industry-focused applications. The ASCO Numatics product line in North America consists of more than 50,000 valves, an extensive selection of air preparation equipment, and a full line of actuation products. ASCO products include solenoid pilot valves, angle body piston valves, linear indicators, redundant control systems, and pressure sensors. The Numatics line covers valve manifolds, cylinders, grippers, filters, regulators, and lubricators. For more information about ASCO Numatics products, visit www.asconumatics.com

About Emerson

Emerson (NYSE: EMR), based in St. Louis, Missouri (USA), is a global leader in bringing technology and engineering together to provide innovative solutions for customers in industrial, commercial, and consumer markets through its network power, process management, industrial automation, climate technologies, and tools and storage businesses. Sales in fiscal 2010 were $21 billion. For more information, visit www.Emerson.com.

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Press Contact: Don Goncalves, 781-793-9380, dgoncalves@tizinc.com

 

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Wednesday, September 14th, 2011

At Shaw Industries, Personalized Ear Plug Fit Testing Overcomes Challenges to Worker Hearing Protection – New Case Study

SMITHFIELD, RHODE ISLAND, USA, September 14, 2011 – In late 2009, Kenny Dillard, faced seemingly insurmountable environmental challenges to the Hearing Conservation program at a Dalton, Ga., manufacturing facility of Shaw Industries Group, Inc., the world’s largest carpet manufacturer and a leading floor covering provider.

Although the company invests in engineering and administrative controls to reduce noise levels, and continues to look for ways to decrease the exposure in the work environment, hearing protection is still needed for many workers. Meanwhile, the local climate, which generates both extreme heat and humidity, often makes the wearing of earmuffs uncomfortable.

The solution, Dillard decided, was to “get personal” with an innovative program that integrates the Howard Leight® VeriPRO® ear plug fit testing system with one-on-one training, resulting in personal validation and self-efficacy.

At Shaw, the new VeriPRO ear plug fit testing program “represents an on-going investment in workers and their personal safety” that resulted in what Dillard believes has evolved into a true one-on-one Hearing Conservation Program. “To get where we are now meant that we had to change our whole mindset — to realize that it’s all about each and every individual — and what fits them well,” he said.

The program proved to be an overwhelming success, earning Shaw the 2011 Safe-in-Sound Award for Best Practices in Hearing Conservation, presented by the National Institute of Occupational Safety and Health (NIOSH) and the National Hearing Conservation Association (NHCA).

The program is also the subject of a new case study which traces Dillard’s progress through each stage of the program’s development and implementation, from “Doubling Up for Safety” to “Ear Plug Fit Testing and Verification” to “Ear Plug Selection, Protection, and Training” to “Personal Validation” – providing a detailed blueprint for safety, industrial hygiene, plant managers, and others to emulate at their own facilities.

Download the free case study at http://hearforever.org/shaw.

About Howard Leight®

Under the Howard Leight brand, Honeywell Safety Products is a leading global provider of passive and intelligent hearing protection solutions, and is the founder of the HearForever™ initiative. For over 30 years, the company and its predecessors have pursued the prevention of occupational noise-induced hearing loss through innovation in hearing protection design, technology, performance and comfort, and the promotion of progressive Hearing Conservation Programs. Leading solutions include the highest attenuating Max® single-use earplug; patented Air Flow Control™ technology for optimal earmuff attenuation; QuietDose™ personal in-ear dosimetry; and the industry-changing VeriPRO® earplug fit testing system. Visit the Howard Leight website at http://www.howardleight.com and follow us on Twitter at http://twitter.com/HowardLeight.

About Honeywell

Honeywell International (http://www.honeywell.com) is a Fortune 100 diversified technology and manufacturing leader, serving customers worldwide with aerospace products and services; control technologies for buildings, homes and industry; automotive products; turbochargers; and specialty materials. Based in Morris Township, N.J., Honeywell’s shares are traded on the New York, London, and Chicago Stock Exchanges. For more news and information on Honeywell, please visit http://www.honeywellnow.com.

This release contains certain statements that may be deemed “forward-looking statements” within the meaning of Section 21E of the Securities Exchange Act of 1934. All statements, other than statements of historical fact, that address activities, events or developments that we or our management intends, expects, projects, believes or anticipates will or may occur in the future are forward-looking statements. Such statements are based upon certain assumptions and assessments made by our management in light of their experience and their perception of historical trends, current economic and industry conditions, expected future developments and other factors they believe to be appropriate. The forward-looking statements included in this release are also subject to a number of material risks and uncertainties, including but not limited to economic, competitive, governmental, and technological factors affecting our operations, markets, products, services and prices. Such forward-looking statements are not guarantees of future performance, and actual results, developments and business decisions may differ from those envisaged by such forward-looking statements.

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Press contact: Don Goncalves, Tiziani Whitmyre public relations, 781-793-9380, dgoncalves@tizinc.com

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Wednesday, August 24th, 2011

New White Paper Examines Clinical Trial Material Production & Testing: What Your Contract Manufacturing Organization is Not Telling You

AGAWAM, Mass.Aug. 24, 2011 — For pharmaceutical manufacturers, delays in starting a clinical trial program due to issues involving the manufacture of clinical trial material (CTM) and the associated fill/finish and release work can make even the most dogged project managers wince in pain. A new, free white paper recommends a proven process of evaluating a cGMP contract manufacturing organization (CMO) to deliver all the required processes needed to release CTM for clinical trial use.

The new white paper, “Clinical Trial Material Production and Testing: Is Your CMO Providing Everything You Need,” explores what pharmaceutical manufacturers must require from a CMO in terms of capabilities and expertise and the critical roles that the contractor must be able to assume in the clinical trial material manufacturing process.

The white paper is available for download from: http://www.microtestlabs.com/clinical-trial-material-production-testing-paper/.

“In order to keep clinical protocols on time and on budget in the CTM manufacturing process, it’s critical that the selected CMO has comprehensive capabilities that are both in-house and readily available,” notes Alexander Mello, author of the white paper and Director of Project Management, Manufacturing, for Microtest Laboratories, a leader in contract manufacturing, aseptic processing and full service pharmaceutical testing.

“Contracting with a CMO without complete in-house expertise will add unnecessary time to the CTM process. In these cases, performing a GMP audit of the CMO, plus all of the other companies (formulators, laboratories, labelers, etc.) that the CMO uses in the supply chain, will add significantly to the overall cost and time for the technical transfer of the product,” he explains.

The new white paper illustrates how the proper selection of a CMO can help meet product schedules and minimize potential restart activities. The paper reviews the roles that the CMO must be able to play in CTM process, from first steps through the completion, and details the key areas of Raw Materials, Formulation, and Final Drug Product (FDP).

The white paper also discusses how a fully-capable CMO will have the ability to perform all the required processes in CTM – including excipient and API release for GMP manufacture, formulation, in-process testing, environmental monitoring, filter integrity testing, and final release testing.

To download the new, free white paper, “Clinical Trial Material Production and Testing: Is Your CMO Providing Everything You Need,” visit http://www.microtestlabs.com/clinical-trial-material-production-testing-paper/.

Mello, the author of the white paper, is Director of Project Management, Manufacturing, for Microtest Laboratories. Mello’s 15 years of experience span Aseptic Fill/Finish, Microbiology, Method Transfer, Stability of Drug Product, Medical Devices/Combo Devices, and Sterilization Sciences. He holds a graduate degree in Biological Sciences and is a Specialist Microbiologist (NRM).

Follow Microtest Labs on Twitter @MicrotestLabs at http://twitter.com/MicrotestLabs.

About Microtest

Microtest is a leader in testing services and contract manufacturing for the medical device, pharmaceutical, and biotechnology industries. Based in Agawam, Massachusetts, U.S.A., the company’s expertise and flexible processes enhance product safety and security, accelerate time to market, and minimize supply chain disruption. For more information, visithttp://www.microtestlabs.com or call 1-413-786-1680 or toll-free 1-800-631-1680.

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Tuesday, August 9th, 2011

ASCO Introduces Stainless Steel Pilot Valves for Offshore Applications

FLORHAM PARK, NEW JERSEY, U.S.A., August 9, 2011 – ASCO Numatics, the world’s leading manufacturer of comprehensive fluid automation, flow control, and pneumatics solutions, has introduced the 8361 Series of stainless steel pilot valves. The series’ unique design eliminates the dormancy or “sticking” problems that can occur in control valves installed in the pneumatic logic panels that control monitoring safety systems in offshore oil and gas production facilities. In addition, the valve line was launched with online tools that permit rapid product configuration and ordering.

“Corrosion-resistance and reliability are essential for safe operation in harsh offshore environments,” said Robert W. Kemple, Jr., executive vice president, sales and marketing – Americas, ASCO Numatics. “The 8361 Series’ innovative, highly reliable, and proven T-seal technology resists the dormancy issues that plague current valves using O-ring seals. O-ring designs can stick upon actuation in low-cycle demand control valve applications. Our research shows that many users routinely hammer the sides of these valves to ensure they function properly,” said Kemple.

The 8361 Series (¼-inch NPT, 3-way, 316L stainless steel) valves are offered in manually operated, air-piloted, and solenoid-piloted versions. They can be configured as breathing and nonbreathing. The non-breathing version isolates internal components from the atmosphere and is internally vented, preventing contaminants such as salt and dust to enter the valve and corrode internal components.

The valve’s balanced design maintains the same flow characteristics when the valve is used in a normally open or normally closed configuration. This provides symmetrical flow that enables more flexible setup of the control panel’s pneumatic logic. The 1.4 Cv provides almost double the flow of comparable spool technology. In addition, the valve’s innovative pilot-selector design allows the same unit to be used as an internally or externally piloted solenoid valve, simplifying ordering and reducing inventory.

The 8361 Series’ solenoid version comes with ASCO’s renowned RedHat solenoid – recognized as the most reliable in the industry. Its 0.55-watt power consumption is three times less than competitive valves.

“Every aspect of this valve has been designed for the highest reliability, minimal maintenance, and lowest cost of ownership,” said Kemple. “For example, the valve’s body is made entirely of 316L stainless steel, and the Elgiloy® and stainless steel spring is designed for corrosion resistance and severe service beyond 1 million cycles.”

Online Tools Enables Rapid Configuration and Ordering

An 8361 Series online toolset is available that allows customers to quickly build a valve that meets a set of specific requirements. It then displays the list price, availability, 3D CAD drawings, and specifications for the configured product. The configurator generates an order code for the valve that permits an immediate online purchase, plus greatly simplifies the reordering process.

The 8361 Series valves can be purchased from ASCO distributors or directly from the company. Most of the valve’s configurations are available through the ASCO Today or 5-day shipping programs.

For more information, contact ASCO at 800-972-ASCO, by e-mail at info-valve@asco.com, or visit http://www.ascovalve.com/Offshore.

About ASCO Numatics

ASCO Numatics, a division of Emerson, offers comprehensive fluid automation solutions, including fluid control and fluid power products, for a wide range of industry-focused applications. The ASCO Numatics product line in North America consists of more than 50,000 valves, an extensive selection of air preparation equipment, and a full line of actuation products. ASCO products include solenoid pilot valves, angle body piston valves, linear indicators, redundant control systems, and pressure sensors. The Numatics line covers valve manifolds, cylinders, grippers, filters, regulators, and lubricators. For more information about ASCO Numatics products, visit http://www.asconumatics.com

About Emerson

Emerson (NYSE: EMR), based in St. Louis, Missouri (USA), is a global leader in bringing technology and engineering together to provide innovative solutions for customers in industrial, commercial, and consumer markets through its network power, process management, industrial automation, climate technologies, and tools and storage businesses. Sales in fiscal 2010 were $21 billion. For more information, visit http://www.Emerson.com.

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Elgiloy is a registered trademark used for metal alloys and owned by Combined Metals of Chicago, L.L.C., Elgin National Watch Company.

Note to Editors:

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Tuesday, June 7th, 2011

New White Paper Helps Medical Device Manufacturers Validate Cleaning Processes

A free white paper that guides manufacturers of medical devices in the validation of their cleaning processes is available from Microtest Laboratories.

It is available for download from: http://microtestlabs.com/cleaning-validation-paper

As many medical devices are made of high-tech materials such as metallic alloys or synthetic plastics, manufacturers may require the use of various agents to aid in the manufacturing process, or produce contaminants that need to be removed. Thus, these products must be cleaned to ensure both patient safety and the continuing functionality of the device.

In the white paper titled, “Five Steps to Validating the Cleaning Process of Medical Devices,” Patrick Kenny, Manager of Analytical Services at Microtest Laboratories, reviews medical device regulation under 21 CFR Part 820 – Quality System Regulation.

Several sections of Part 820 can be directly related to medical device cleanliness. For manufacturers, the challenge is to validate the cleaning process to ensure the devices are free of residue (chemical and particulate) in order to ensure patients are safe.

In the paper, Kenny presents a five-step process that provides a framework to assist manufacturers of medical devices in their cleaning validation efforts:
#1: Evaluate the Process, Determine the Potential Contaminants
#2: Determine the Limits
#3: Identify the Analytical Test
#4: Validate the Method for Use
#5: Validate the Cleaning Process

Download a free copy of “Five Steps to Validating the Cleaning Process of Medical Devices,” at http://microtestlabs.com/cleaning-validation-paper.

At Microtest Labs, Kenny leads the services group performing medical device and pharmaceutical analytical testing. He holds a M.S. degree in Chemistry and has spent the past 13 years working in QC, R&D and manufacturing laboratories.

About Microtest Laboratories
Microtest Labs is a leader in testing services and contract manufacturing for the medical device, pharmaceutical, and biotechnology industries. Based in Agawam, Massachusetts, U.S.A., the company’s expertise and flexible processes enhance product safety and security, accelerate time to market, and minimize supply chain disruption. For more information, visit http://microtestlabs.com or call 1-413-786-1680 or toll-free 1-800-631-1680. Follow Microtest Labs on Twitter @MicrotestLabs at http://twitter.com/MicrotestLabs

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Wednesday, May 11th, 2011

“Five Critical Factors for Selecting Fieldbus Valve Manifolds” — New White Paper from Numatics, Inc.

FLORHAM PARK, N.J. — May 10, 2011 — Fieldbus valve manifolds are replacing conventional hardwired solutions on a variety of highly automated machines in a wide variety of applications and industries. A new white paper, “Five Critical Factors For Selecting Fieldbus Valve Manifolds,” from Numatics, Inc., guides original equipment manufacturers (OEMs) and end users in the selection of the best solutions for their given applications.
The paper is available for download from http://www.numatics.com.
“Fieldbus valve manifolds find wide utility in packaging, automotive/tire, and material handling applications, as well as in the pharmaceutical, chemical, water, and wastewater industries,” said white paper author Enrico De Carolis, director of technology development at Numatics, Inc.
In the white paper, De Carolis presents the five crucial factors that controls engineers, specifiers, and buyers must consider before selecting pneumatic fieldbus valve manifolds — commissioning, distribution, modularity, diagnostics, and recovery — while outlining the shortcomings of conventional approaches.
In addition, De Carolis also discusses new designs that offer substantial improvements in the application, performance, and maintenance of these valve manifolds from the end users’ and OEMs’ points of view.
“Fieldbus valve manifolds more easily perform vital functions by integrating communication interfaces to pneumatic valve manifolds with input/output (I/O) capabilities. This allows programmable logic controllers (PLCs) to more efficiently turn valves on and off and to channel I/O data from sensors, lights, relays, individual valves, or other I/O devices via various industrial networks. The resulting integrated control packages can also be optimized to allow diagnostic benefits not previously available,” he said.
Follow Numatics, Inc. on Twitter at http://twitter.com/asconumatics and on Facebook at http://ht.ly/4jGNg.
Emerson Industrial Automation
Emerson Industrial Automation, a business of Emerson, delivers manufacturing solutions designed with leading technologies — including mechanical, electrical and ultrasonic — to provide the most advanced industrial automation possible for numerous and diverse industries worldwide. The company’s wide range of products and systems used in manufacturing processes and other equipment includes motion control systems, plastics joining, precision cleaning, materials-testing equipment, fluid control valves, alternators, motors, and mechanical power transmission drives and bearings. For information, visit www.emersonindustrialautomation.com.

About Emerson
Emerson (NYSE: EMR), based in St. Louis, Missouri (USA), is a global leader in bringing technology and engineering together to provide innovative solutions for customers in industrial, commercial, and consumer markets through its network power, process management, industrial automation, climate technologies, and tools and storage businesses. Sales in fiscal 2010 were $21 billion. For more information, visit www.Emerson.com.

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Press Contact: Don Goncalves, 781-793-9380, dgoncalves@tizinc.com
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Tuesday, April 26th, 2011

ASCO Numatics to Merge Miniature Valve Products Under the ASCO Brand

FLORHAM PARK, NEW JERSEY, USA April 26, 2011ASCO Numatics, the world’s leading manufacturer of comprehensive fluid automation, flow control, and pneumatics solutions, announced today it will merge all of its ASCO and Numatics miniature valve product lines under the ASCO brand, effective immediately. The products include 25 series of direct-acting miniature solenoid valves and manifolds.

“In this merger, we are taking the best products from the former ASCO Scientific and Numatics Miniature Pneumatic Group product lines to create a broader, more customer-focused family of ASCO Miniature Valve Products,” said Robert W. Kemple, Jr., executive vice president, sales and marketing — Americas, ASCO Numatics. “Our capability to rapidly customize these miniature valve solutions means product asco-miniature-valve-productsengineers will not have to change their designs to incorporate our products.”

ASCO miniature valve products are ideal for engineers developing medical equipment and analytical instrumentation. The solutions can be customized to easily interface with existing product designs. Valve specifications can be adjusted to achieve the desired performance, and specific wire terminations can be selected for easy plug-and-play connectivity.

“ASCO’s heritage of product quality and reliability will be highly attractive for critical medical system applications such as oxygen concentrators, critical-care ventilators, dialysis machines, and blood analyzers,” said Kemple. “All of our miniature valve products will be built in a clean room environment to eliminate airborne contamination, and complete assemblies will be tested to each customer’s requirements.”

ASCO miniature valve products are supported by the largest engineering and technical support team in North America. “Our technical and field sales personnel will help customers identify specific miniature valve solutions that will reduce cost and extend equipment life,” Kemple said.

To receive the new ASCO Miniature Valve Products catalog or get more information, call ASCO at 800-972-ASCO, e-mail info-valve@asco.com, or visit www.ascovalve.com/miniature.

About ASCO Numatics

ASCO Numatics, a division of Emerson, offers comprehensive fluid automation solutions, including flow control and pneumatics products, for a wide range of industry-focused applications. The ASCO Numatics product line in North America consists of more than 50,000 valves, an extensive selection of air preparation equipment, and a full line of actuation products. ASCO products include solenoid pilot valves, angle body piston valves, linear indicators, redundant control systems, and pressure sensors. The Numatics line covers valve manifolds, cylinders, grippers, filters, regulators, and lubricators. For more information about ASCO Numatics products, visit www.asconumatics.com

About Emerson

Emerson (NYSE: EMR), based in St. Louis, Missouri (USA), is a global leader in bringing technology and engineering together to provide innovative solutions for customers in industrial, commercial, and consumer markets through its network power, process management, industrial automation, climate technologies, and tools and storage businesses. Sales in fiscal 2010 were $21 billion. For more information, visit www.Emerson.com.

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Notes to Editors:

Press Contact: Don Goncalves, Tiziani Whitmyre, Inc., 781-793-9380, dgoncalves@tizinc.com

Download high resolution image for publication: http://bit.ly/ASCOMiniature

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Monday, April 11th, 2011

New White Paper: “The Insider’s Guide to Applying Miniature Solenoid Valves,” from ASCO Valve

FLORHAM PARK, N.J. — April 11, 2011 — A new white paper, The Insider’s Guide to Applying Miniature Solenoid Valves, consolidates the expert views of designers and manufacturers to provide a step-by-step resource for applying miniature solenoid valves for myriad uses across multiple industries.

The paper is available to download from http://bit.ly/h0iq7f.

“Equipment designers frequently must incorporate miniature solenoid valves into their pneumatic designs. These valves are important components of medical devices and instrumentation as well as environmental, analytical, and similar product applications,” said white paper author Mike Elsigian, marketing manager, ASCO Valve, Inc.

In the white paper, Elsigian defines which requirements are critical for common applications. He details how the selection of miniature solenoid valves for the design of a given device usually involves finely balancing tradeoffs among competing pressures for reliability, service life, light weight, higher flow, optimized power use, standards compliance, and more.

Elsigian also highlights the introduction of newer valve technologies that can lessen or eliminate difficult compromises — while increasing performance. “New miniature solenoid valve technologies represent the fusion of several innovative approaches to meet the widest possible range of demands from knowledgeable designers across multiple industries,” he said.

“All too often, these designers find themselves frustrated as they face compromise after compromise. Pressure for increasingly miniaturized devices complicates every step of the design and valve selection process. And missteps can wreak havoc,” he said. “We’re hoping that the expertise we provide will assist designers in achieving the balance they need for success among the variety of often-contradictory performance requirements demanded by their applications.”

Download the new white paper, “The Insider’s Guide to Applying Miniature Solenoid Valves,” at http://bit.ly/h0iq7f.

Follow ASCO on Twitter at http://twitter.com/ascovalve. Find ASCO on Facebook at http://facebook.com/ascovalve.

Emerson Industrial Automation

Emerson Industrial Automation, a business of Emerson, delivers manufacturing solutions designed with leading technologies — including mechanical, electrical and ultrasonic — to provide the most advanced industrial automation possible for numerous and diverse industries worldwide. The company’s wide range of products and systems used in manufacturing processes and other equipment includes motion control systems, plastics joining, precision cleaning, materials-testing equipment, fluid control valves, alternators, motors, and mechanical power transmission drives and bearings. For information, visit www.emersonindustrialautomation.com.

About Emerson

Emerson (NYSE: EMR), based in St. Louis, Missouri (USA), is a global leader in bringing technology and engineering together to provide innovative solutions for customers in industrial, commercial, and consumer markets through its network power, process management, industrial automation, climate technologies, and tools and storage businesses. Sales in fiscal 2010 were $21 billion. For more information, visit www.Emerson.com.

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Press Contact: Don Goncalves, 781-793-9380, dgoncalves@tizinc.com

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Friday, April 8th, 2011

H&V’s Technostat Plus nominated for EDANA Innovation Award

East Walpole, Mass – April 8, 2011 - Hollingsworth & Vose has been nominated for the EDANA Innovation Award for its Technostat® Plus filter media. Technostat Plus is an electret air filter media for use in respirators, HVAC, medical, vacuum cleaners and cabin air filter applications.

H&V’s Technostat Plus is an extension of the Technostat product family, which achieves higher filter media performance and enhanced processability. Technostat products offer high sub-micron efficiency, high dust holding capacity, extremely low pressure drop and a stable shelf life. As with H&V’s recently introduced Capaceon® product platform, Technostat breaks the link between filter media basis weight and performance. For example, one media design offers pressure drops which are nearly half that of current media at the same basis weight. Another design retains the same performance level of current Technostat while offering a 20-25% basis weight reduction. Technostat Plus offers filter designers greater flexibility and increased life time value.

European Nonwovens Industry Association EDANA will present their annual awards on April 12th, the opening day of the INDEX 11 show in Geneva. These awards are described by EDANA as “the highest accolade for the best examples of excellence in our industry”.

For further information on Technostat Plus, please contact Bastian Keil at Bastian.Keil@hovo.com

Established in 1843, Hollingsworth & Vose Company (http://www.hollingsworth-vose.com) is a global leader in the supply of technically advanced engine, high efficiency and liquid filtration media, battery separator materials and industrial nonwovens. The company operates manufacturing sites and research centers in the Americas, Europe and Asia.

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Press contact: Don Goncalves, Tiziani Whitmyre, dgoncalves@tizinc.com 781-793-9380

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