TJ/H2b provides material and/or equipment specific diagnostic evaluations and consultation services to give as complete an analysis as possible. Substantial individual projects are routinely handled with no loss in turnaround time or quality performance. TJ/H2b has developed three proprietary diagnostic evaluations for differing types of high voltage electrical equipment: Breaker Oil Analysis (BOAÔ) for oil filled circuit breakers, Tap changer Activity Signature Analysis (TASAÔ) for on-load Tap Changers and Transformer Condition Assessment (TCAÔ) for oil insulated transformers of any size.
Aurora Biomed's specializes in elemental analysis instruments and supply spectrometers to suit your needs and application for any elemental analysis requirements. For any trace element detection ranges in the parts per million (ppm), parts per billion (ppb) and parts per trillion (ppt) level, we have the solution for you! read more ...
AvTech Laboratories is a full-service Contract Research Organization (CRO) serving the pharmaceutical industry since 1990. Operational and quality systems in place at AvTech Laboratories ensure that we deliver on our commitment to scientific excellence and regulatory compliance. AvTech's philosophy incorporates a comprehensive multitiered review of all data. Results of our regulatory and client audits confirm our exemplary reputation and high standards. Our commitment to service is facilitated by open lines of communication with our clients. AvTech utilizes state-of-the-art analytical technology to support clients' needs as they discover and develop new pharmaceutical candidates for approval by regulatory agencies. In-house techniques include HPLC utilizing both Fluorescence and UV Detection, Dissolution Testing, Immunoassays, Small Molecule X-ray Crystallography, radioanalysis (sample oxidation and liquid scintillation analysis), GC, GC/MS and LC/MS/MS. Mass Spectrometry equipment includes Sciex and Micromass platforms. Available sample storage conditions range from -70° C freezers to environmental chambers covering the range of ICH conditions for temperature and humidity.
What We Do: WaveSense develops, manufactures, and markets breakthrough analytical nanotechnologies for use in cellular and molecular assay markets. Some of the applications that we are actively engaged in consist of drug discovery, rare cell detection in blood and bone marrow, nucleic acid tests for infectious disease, bio-defense, veterinary diagnostics, and regenerative medicine. Our Proprietary Technology: Our patented and hierarchy technology is called Xenographic Retention ChromatographyÔ (XRC) - branded as EpiSepÔ, which is a lateral flow separations platform that provides rapid, advanced detection and characterization of live cells, proteins, and/or genes. Researchers can then harvest the targets for interrogation purposes within their desired application. Our Value Proposition: We developed EpiSepÔ because current assays that detect rare targets are outgrowing the capabilities and efficiencies of platforms that are commonly used to perform these tests. Our EpiSepÔ platform, and extensive line of leading-edge assays, are revolutionary to the analytical industry as they fulfill a critical demand to significantly improve test sensitivity and workflow procedures, while reducing operational costs and complexity. Users of Our Products: End users of our products consist of reference laboratories, pathologists, and researchers that perform a wide variety of analytical tests for research purposes. Why We Do This: We strive to improve the quality and length of life by discovering and applying leading-edge nanotechnologies to life science research. We adopt this approach with an added interest to create value for our employees and shareholders. Our Background: WaveSense is a privately held California company that was founded in 1999 by Christopher Feistel and Robert Coleman. Individually and collectively, Feistel and Coleman have participated as principal inventor, co-founder, chairman, president and/or CEO of more than 10 medical device companies resulting in successful organizations with combined valuations exceeding one billion dollars. Our Facility - Our corporate offices and laboratory are housed in an 8500 Square Foot facility located at 15339 Barranca Parkway, Irvine, CA 92618. Thank you for visiting our web site.
Serim Research Corporation develops, manufactures, and markets test strips based on Serim's dry reagent technology. Technology created and developed at our facility includes colorimetric chemistries, reagent/membrane impregnation, and test strip fabrication. In business since 1988, our fully integrated Research & Development/Manufacturing Center is located in Elkhart, Indiana in a new, state-of-the art, 32,630-square-foot, FDA-registered facility certified to ISO 9001:2000 and ISO 13485:2003 (specific for medical devices).
Hometest® is an environmental testing company developed to help prevent the health, legal and financial consequences of exposure to environmental hazards. Hometest® does this by making testing products, industrial hygiene services, analysis, and environmental training related to these hazards affordable, simple to use, and reliable. All samples are analyzed in the EPA-recognized lab, METS Laboratories, thereby assuring users of the highest degree of accuracy and test integrity. Hometest® offers a full range of analytical testing for: Lead based paint dust Drinking water quality Mold/Mildew Allergens Radon gas Environmental concerns in residential housing are receiving major attention from the national health care industry and regulators. These concerns are being driven by new discoveries in the health care industry that demonstrate how even small amounts of environmental contaminants present in homes have devastating effects on the occupants, particularly children, pregnant women and family pets. As a result, in an effort to educate the public, there have been new federal and state laws enacted requiring disclosure of environmental issues during any real estate transaction, whether it is a purchase or a rental. The media is publishing or broadcasting a feature story almost every day about environmental contaminants in properties and the need to test for these hazards. Additionally, health care industry policies are shifting from secondary prevention to primary prevention. Secondary prevention involved testing children to determine if they had been exposed to environmental contaminants. If tests showed that a child had been exposed, the child's home would then be tested to determine how and where the exposure occurred, as well as how to correct the problem. As the health effects of childhood exposure to environmental hazards are irreversible in many cases, health care professionals have agreed that it is clearly more responsible to test the child's home environment early to prevent the child from being exposed, rather than waiting until the child has been exposed and then trying to treat the health effects. In other words, preventing the problem, rather than treating the effects of the problem, is becoming the norm. With increasing regularity, environmental problems in housing are being discovered after the sale. With equal regularity, home inspectors, real estate agents, and sellers are being held liable for these conditions. New residents may experience the ill effects of mold, lead, radon and drinking water contamination that perhaps did not effect the prior residents. Many people make numerous trips to the doctor's office before the root of their health problems is identified. Affected individuals, many times, choose to litigate against the sellers, home inspectors and real estate professionals involved in the property transaction. There is a solution to this recent trend which presents an opportunity for Home Inspectors. The solution is to provide environmental testing as part of the home inspection process. The opportunity is for Home Inspectors to increase their income while providing a needed service to their customers. An added bonus is the protection this testing will provide by limiting liability on the Inspector's part. The actual sample collection process is easy and adds very little time to the inspection process. Hometest® provides a host of goods and services, designed to take the mystery out of environmental testing and making this testing easy and understandable. We provide excellent support to Home Inspectors, including classroom Mold & Healthy Home training classes, a self-study course on environmental testing with regards to the home inspection known as the Environmental Training Course, instructional and promotional videos, marketing assistance, and updates on current environmental trends in the industry. Our laboratory services include not just accurate analyses, but also understandable reports, easy-to-use and convenient sampling kits for lead, radon, mold and drinking water, knowledgable Sales Executives, and a full-time Customer Service department to attend to your every need. Hometest® 's convenient testing kits feature packaging all supplies an inspector normally uses into a kit. After collecting samples, all an inspector need do is drop the kit into the nearest UPS drop box for overnight delivery to the laboratory. Additionally, the kits include complete detailed instructions on how and where to collect samples. The user simply purchases the kit, collects the samples following the instructions, sends the samples to Hometest® and receives easily understood test results. As you see, we are much more than just a laboratory. We are your partner in success. Our training programs, business development and marketing support help us to help you be as successful as possible. Our laboratory services are quick, affordable and accurate. We understand your business, have a vested interest in helping you to succeed, and pledge ourselves to that end every day.
NAEJA was established in 1999 with a rollover of assets, including staff, equipment and intellectual property, from SynPhar Laboratories Inc. and research contracts from DrisCorp Inc. What began as a full fledged pharmaceutical company with an extensive intellectual property portfolio and a proven track record has evolved into an internationally respected pharmaceutical outsource service provider. NAEJA has carved a unique niche in the outsource industry offering extensive discovery experience and expertise. The flexibility NAEJA offers to custom design drug discovery services has kept NAEJA at the forefront of the industry. NAEJA's commitment to global health, extensive drug discovery experience and attention to continual improvement are key factors that contribute to NAEJA's success and keep the company at the forefront of the industry. NAEJA will continue to focus on delivering optimum service in a continued commitment to the pharmaceutical industry. It is through international teamwork that we must wage our war against illness and NAEJA will continue on with its mission making significant contributions as a valuable team member.
Columbia Analytical Services, Inc., established in 1986, is an employee-owned, full-service analytical laboratory company. Columbia Analytical has locations throughout the United States with more than 147,000 square feet of laboratory and client service center space. The company offers a complete range of laboratory services, including: Analytical testing dots Environmental testing of air, water, wastewater, soil, sludge, solids, waste oil, solvents, hazardous waste, sediments and tissues Micro-elemental analyses including analysis for C, H, N, O, S, metals and halogens on a wide variety of matrices Pharmaceutical and nutraceutical analysis Process and quality control testing for many industries including pulp and paper, electronics, pharmaceutical and nutraceutical industries Analytical method development Sampling, field and mobile laboratory services Technical consulting including project and data management capabilities Our staff of chemists, biologists, microbiologists, computer scientists, field samplers, project managers and administrative personnel is dedicated to meeting our customer's needs. Our diverse educational backgrounds and experience provide Columbia Analytical with the comprehensive skills that a modern analytical laboratory network requires. We are committed to giving our staff the necessary resources to maintain their expertise and stay abreast of our industry's ever-changing technology. This commitment to our staff and to our rigorous quality assurance program helps ensure that we give our clients the highest quality analytical services available. Our over-riding goal as a company is to exceed our clients' expectations by providing sound science, unsurpassed testing quality and extraordinary customer service.
With over 20 years of microparticle experience,Seradyn provides innovative solutions for the world's best medical, diagnostic, and life science companies. We work behind the scenes to produce: The most accurate and precise digoxin test on the market. The most widely used magnetic particle for sample prep in the Human Genome Project. The AACC standard for recombinant CK-MB antigen. Seradyn has built a reputation as a world class manufacturer of many OEM assays and highly specific particles for the largest companies in the world. We are committed to your success by providing raw materials and the timely technical support you require. With over 20 years of experience in providing solutions for the world's top companies, we continue to set the standard for the development and manufacture of microparticles and OEM immunoassay products. We're focused on a range of therapeutic drug monitoring homogeneous immunoassays utilizing multiple analytical technologies. Seradyn's assay technologies include turbidimetry, fluorescence polarization and chemiluminescence. Our products are sold by OEM arrangements and through distributors throughout the world. We also focus on microparticles used as a raw material for these clinical immunoassays and molecular biology applications. The microparticles are used in a wide variety of diagnostic assays, as well as nucleic acid isolation, amplification, genotyping and sequencing applications. Seradyn also further enhances its value to our partners by supplying monoclonal antibodies and recombinant antigens.
Azopharma specializes in drug development support for the pharmaceutical industry. We are experts at formulations, custom synthesis, isolation/purification, elucidation, characterization, method development and validation, clinical supplies for Phase I. Azopharma supports product development for: Drug substances and excipients Oral dosages (tablets, capsules) Topical dosages (creams, ointments, lotions) Liquids dosages (injectables, suspensions) Inhalation dosages (MDI, DPI, Nasal) Biotech products Nutraceuticals Medical devices We can perform cGMP compliant analyses using a variety of analytical techniques including FT-IR, NMR, SEM/EDXA, DSC, GC, HPLC and Direct Probe MS. We are also capable of combining these tools with proprietary polymer and physical testing methodologies to provide novel approaches to product release testing, package suitability and stability monitoring studies. Azopharma is FDA registered and audited, DEA licensed and cGMP compliant. We welcome visits to our facility for audits or to outline a study that meets your specific needs.
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