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Test Chambers
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Drug test chamber, ozone test chamber, plant grown chamber, salt spray test chamber, sand test chamber, temperature and humidity test chamber, UV test chamber, xenon test chamber
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Multi-omics Analysis Package
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The Multi-omics Analysis Package, developed for metabolic engineering applications, provides the ability to automatically generate metabolic maps and perform a variety of data analysis for the vast data generated in fields like metabolomics, proteomics and flux analysis. It offers a powerful platform to support drug discovery, bioengineering and other life science research applications.
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ASCA Pilot Program Participation
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Compatible Electronics, Inc. is a testing laboratory participant under the United States Food and Drug Administration’s Accreditation Scheme for Conformity Assessment (FDA ASCA) pilot program. We are listed under ASCA ID# TL-80, TL-81 and TL-82.
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Medical Equipment
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We develop solutions for demanding medical applications. Whether a Home Healthcare CPAP or complex Robotic Surgical System, Haydon Kerk Pittman can deploy a solution designed to your program requirements. We offer lube free systems for clean, maintenance-free operation; specialty materials for radiation, autoclaving and chemical environments; smooth and quiet operation for patient facing applications; and miniature and micro product designs for precision fluid pump and drug delivery systems.
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Handheld Narcotics Analyzer
TruNarc™
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The global drug problem is increasing, with trafficking of meth, heroin, and emerging threats like fentanyl, and carfentanil, impacting communities worldwide. Law enforcement officials need to quickly identify suspected narcotics in the field to help keep drugs, and drug dealers, off the streets. Now with the expanded v1.7 library, the Thermo Scientific™ TruNarc™ Handheld Narcotics Analyzer enables officers, customs, border control, and other personnel to scan more than 415 suspected illicit substances in a single, definitive test.
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NVIDIA Systems
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NextComputing’s Data Science Workstations featuring NVIDIA GPUs from PNY dramatically accelerate data analytics time to insights, enabling breakthrough data preparation, model development and training performance. These powerful workstations can aid in the advancement of medicine and research enabling scientists to tackle interoperable data development of AI-based intelligent applications unique to their workflows and accelerate areas like image analysis, scientific research, and drug discovery.
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Drug Stability Test Chamber
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Sanwood Environmental Chambers Co ., Ltd.
If you want find complete details about Integrated drug stability test chamber, Drug stability test chamber, Chemical drug stability test chamber, New designed integrated drug chamber, Good quality integrated drug test chamber - China Sanwood Environmental Chambers Co., Ltd. The scientific method to create a drug for a long time to failure evaluation of stable temperature, humidity and light environment for pharmaceutical enterprises to accelerate drug test, long-term test, high humidity and strong light test, is the best choice for pharmaceutical companies and drug stability test program.
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Autoinjector Testing System
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Instron’s Autoinjector Testing System is designed to perform full functionality testing on a wide variety of drug delivery devices, including safety syringes and both needle shield and button-activated formats. Developed in collaboration with pharmaceutical manufacturers and CDMOs, the system captures essential performance requirements such as activation force, injection time, dose accuracy, needle depth, and click detection. It supports compliance with international standards like ISO 11608 and can be configured for integration with collaborative robots to enhance automation and throughput.
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Pharmaceutical Analysis Contract Services
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Specialist pharmaceutical analysis contract services to support development programs (R&D), regulatory submissions, GMP manufacturing and post-marketing requirements Pharmaceutical analysis contract services can play an important role in your the development process and GMP manufacturing. Concerns about drug safety, costly development programs, complex manufacturing, market demands for evidence-based data and increased regulatory requirements are all issues that can be addressed through a better understanding of your drug substance, drug product or manufacturing process which, in turn, can only be achieved through experienced analytical studies and robust analytical data.
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pH Ion Meter
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pH Ion Meters can be used in research institutions, and at a variety water quality related production sites in the mining, agriculture, forestry and fishery industries, for measuring the ionic concentration and various laboratories for the researches and drug manufacture processes. In addition, it is used in agriculture to measure the salinity levels of surface water and of soil samples and also measure the quality of water.
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On-Column Derivatization GC-MS System
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There's been a surge of public interests in social problem on abused drugs such as methamphetamine and MDMA. In case such amine stimulants are analyzed using urine sample, the derivatization by using trifluoroacetic acetyl is normally processed before GC/MS analysis. However, this derivatization method requires time and effort.
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Software Adaptive Modeling & Simulation of Nanosystems
SAMSON
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SAMSON is the quickly growing platform for integrated molecular design. SAMSON's goal is to make it faster for everyone to design drugs, materials and nanosystems. For fun, or to build a better tomorrow through science and innovation in medicine, energy, materials, electronics, education, and more. SAMSON is available on all major operating systems.
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Comparative Dissolution Tester
CD14 Comparative Dissolution Tester
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The Teledyne LABS 14-vessel CD14 Comparative Dissolution Tester runs two methods simultaneously or independently—ideal for bioequivalence studies of generic vs. innovator drug formulations. The 14 stirring positions allow for 6+1 or 12+2 configurations for improved workload efficiency in R&D, formulations, QC, and stability-test labs. With digital temperature probes at 12 positions the CD14 comparative dissolution tester is able to test two different formulations with separate settings for every parameter under the same temperature conditions.
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LC/MS/MS Rapid Toxicology Screening System
Ver.3
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This system improves the efficiency of simultaneous LC/MS/MS analysis methods by allowing the user to start analysis without time-consuming steps such as consideration of separation conditions and MS parameter optimization. Rapid simultaneous analysis methods with analysis times under 15 mins are included for 235 compounds including drugs of abuse, psychoneurotic drugs and sedatives. The system also provides optimised conditions for synchronised survey scans used in screening measurements (conditions adopted for the product ion spectrum as a threshold value for the intensity in MRM).
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LC/MS/MS Forensic Toxicology Database
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The database includes information on drugs of abuse, hypnotics, psychotropics, pesticides, prescription drugs and natural toxins.
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Multiparameter Analyzers
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Multi-parameter analyzers can be used in processes such as wastewater treatment, drinking water supply and is necessary to support life and treatment developments. In addition, the meter can be used in research institutions, and at a variety water quality related production sites in the mining, agriculture, forestry and fishery industries, for measuring the ionic concentration and various laboratories for the researches, drug manufacture processes, agriculture to measure the salinity levels of surface water and of soil samples, environmental protection, cosmetic industry food processing
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Handheld Raman Analyzer
TacticID®-1064
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The TacticID®-1064 is a field-ready handheld spectral analysis instrument designed for non-contact forensic analysis by safety personnel and first responders, including law enforcement personnel, bomb squads, customs and border patrol, hazmat technicians, and more. The TacticID®-1064 utilizes proven Raman spectroscopy, allowing users to get real-time actionable identification of unknown chemicals, explosives, narcotics, pharmaceutical drugs and many other substances while reducing operational uncertainty and response time. The TacticID®-1064 includes a comprehensive library of over 10,000 substances. In addition, users have flexibility to create their own libraries. By utilizing the 1064nm wavelength, the TacticID®-1064 avoids fluorescence, allowing users to get results in less than 1 minute even when working with tough street samples.
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Measuring Visual Functions
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Cambridge Research Systems Ltd
Whether you need Metropsis ready-to-run visual function assessment unit for clinical research or drug trials, or a fully programmable software tool for vision science, like the Visual Psychophysics Engine, or Psykinematixs, we have the solution.
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Aerosol Optical Tweezers
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Bristol Industrial & Research Associates Ltd
Biral Manufacturers Aerosol Optical Tweezing instruments that offer the ability to study individual particles over indefinite periods. Developed in collaboration with the Bristol Aerosol Research Centre at the University of Bristol the instruments are used in research applications such as atmospheric chemistry, pharmaceutical drug development and basic aerosol research.
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Empowering Traditional Mass Spec
ZipChip
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The ZipChip™ separations platform uses integrated microfluidic technology to prepare, separate and electrospray biological samples directly into traditional mass spectrometers (MS). In less than 3 minutes per sample, the cost-effective ZipChip system enables analysis of a broad range of matrices from growth media to cell lysates, blood, plasma, urine, and biopharma products. Each chip provides answers on analytes from small molecules up to intact proteins, antibodies and antibody drug conjugates (ADCs). This platform provides better separation quality than most liquid chromatography (LC) instruments – in a fraction of the time – all with full MS identification behind every separations peak.
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Application Specific LC Systems
Nexera FV
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Taking Online Dissolution Testing Into the New Era of Ultra High Performance Chromatography Nexera FVDissolution tests are widely used in original pharmaceuticals development and quality control and for bioequivalence tests in generic drugs.
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Microscopic Melting Point Meter
DRK8029
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Shandong Drick Instruments Co., Ltd.
Determination of the melting point of the substance. Mainly used for the determination of drugs, chemicals, textiles, dyes, perfumes and other organic crystal, the microscope. Measured either by capillary method, and the slides are available - coverslip (hot stage method).
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Dissolution Testing
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Agilent offers laboratories the pharmaceutical dissolution testing apparatus, dissolution accessories, and dissolution software for efficient and reliable dosage form testing. Extensive dissolution skills training is also offered to meet the needs of all busy laboratory analysts. Feel confident with Agilent dissolution testing apparatuses. All systems meet the international harmonized guidance requirements defined by USP, EP, CP, IPC, and JP for effective drug dosage form testing. Laboratory analysts can efficiently meet data integrity requirements too. Working to Title 21 Code of Federal Regulations (CFR) part 11 compliance standards is readily achieved using Agilent dissolution testing software.
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Tablet Hardness Testers
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Teledyne LABS offers both manual and automated tablet hardness testers. Tablet hardness testing is a method of determining mechanical properties of a drug product, typically oral dosage forms such as a solid dose tablet. Tablet breaking force (commonly called tablet hardness) is a crucial characteristic in the manufacture of solid dose formulations. Tablet hardness testing is a major step in tablet consistency and quality control.
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Photostability and NDT Radiometer
R203
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Most drugs and pharmaceutical compounds are required to be tested for their photostability under prolonged exposure to visible and ultra violet light.Additionally, when using fluorescing dyes in crack detection the ambient visible light levels and the intensity of the ultra violet source have to be controlled.
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Energy Dispersive X-ray Fluorescence Spectrometer
Pharmaceutical Elemental Impurities Analysis System
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Control of Elemental Impurities in Pharmaceuticals In the pharmaceutical industry, the analysis of elemental impurities is necessary to ensure the safety of pharmaceuticals. In December 2014, the "Guideline for Elemental Impurities" (Q3D) was issued by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), consisting of representatives from Europe, the U.S. and Japan. In Japan, the "Guideline for Elemental Impurities in Drug Products" (PFSB/ELD Notification 0930 #4 from the Ministry of Health, Labour and Welfare) was issued, and will be applied to new drug products submitted for approval after April 1 2017. For 24 elements categorized in Class 1 to Class 3, residual quantities in pharmaceutical drug products must be controlled within permissible limits. Although ICP-AES and ICP-MS are used for precise analysis of elemental impurities, X-ray fluorescence spectrometers can be used as an alternative analysis method. This is because they can quantitatively and qualitatively analyze a variety of elements nondestructively, and without chemical pretreatment, unlike ICP-AES and ICP-MS systems. The X-ray fluorescence spectrometry has been adopted as a general method of analysis in the U.S Pharmacopeia and the European Pharmacopoeia. (USP<735>, Ph.Eur.2.2.37)
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Single Plane Scanners
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Specifically designed for retailers that require high performance in a compact, horizontal or vertical form factor, the single plane products are tailored for medium to high volume POS applications at an affordable price. These products are particularly effective for grocery, department, drug, do-it-yourself centers and general retail environments.
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GC/MS Forensic Toxicological Database
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The GC/MS Forensic Toxicological Database contains information for the simultaneous screening of toxicological substances including drugs of abuse, psychotropic drugs, medical drugs and pesticides. Version 2 adds 1198 compounds to the previous version for a total of 2210 compounds in the database. It also includes optimized methods for headspace analysis of alcohol and volatile toxic substances such as cyanides and azides, providing total support for GC/MS toxicology analysis.
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ASAPrep
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Compound isolation, purity analysis, and impurity analysis in pharmaceutical drug development presents increasing challenges to the industry as there is a clear need to enhance productivity and ensure compliance with evolving regulatory requirements. Such challenges are common to the development of new chemical entities, generic pharmaceutical manufacturing and contract research organizations. To help enhance productivity in compound purification and isolation Shimadzu has developed ASAPrep (Automated Scale-up from Analytical to Preparative), a unique solution to automate and optimize the purification process.
