Showing results: 1 - 15 of 206 items found.
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RA802 -
Renishaw Inc.
The RA802 Pharmaceutical Analyser is a compact benchtop Raman imaging system designed exclusively for the pharmaceutical industry. It rapidly determines API/excipient domain statistics enabling you to formulate tablets more efficiently. With Renishaw's LiveTrack™ focus-tracking technology, the RA802 can efficiently analyse uneven, curved, or rough surfaces at incredible speeds and without any sample preparation. Look at tablets, powders, granules and liquids in their original form.
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Physical Sciences Inc.
Our pharmaceutical products target aseptic fill/finish manufacturing applications including manufacturing operations that utilize barrier isolators and lyophilization, often used to process the fastest growing segment of the pharmaceutical industry, biopharmaceuticals.
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CP series -
Clima Temperatur Systeme
Our Pharmaprfschrnke have been specifically designed for long-term and stability testing in the pharmaceutical industry and have very small tolerances. With these test chambers can be the shelf life of different products such as check medicines and identify suggestions for optimal storage conditions.
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Shimadzu Corp.
Currently, there is a strong demand for the introduction of development, manufacturing and control systems in accordance with GxP at pharmaceutical manufacturing and development sites. And, in pharmaceutical manufacturing, water quality control in line with the GxP guidelines is also required for water used as raw materials and rinsing water. The TOC-V/L Series conforms not only with USP (United States Pharmacopeia) and JP (Japanese Pharmacopeia) but also with other world standards (EPA, ASTM, JIS, ISO, etc.), and demonstrates its outstanding performance in TOC control and cleaning validation of pharmaceutical water.
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Fortress Technology Inc.
Stealth Pharmaceutical metal detectors are custom manufactured to suit Pharmaceutical and/or Nutraceutical applications. Stealth detectors use digital signal processing technology and have high sensitivity levels to ensure the detection of the smallest ferrous, non-ferrous and stainless steel contaminants. The built-in data collection software with USB connectivity establishes the Stealth as an effective critical control point complying with stringent HACCP regulations.
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Fortress Technology Inc.
The Phantom Pharmaceutical metal detector provides the ideal solution for detection and rejection of the smallest contaminants in tablets and capsules. With its current GMP design and construction suited for FDA compliance, the system meets the stringent QA requirements of the pharmaceutical industry. A free IQ/OQ Validation package is included. Built with a rugged mirrored stainless steel exterior, contact parts are all removable for cleaning without the need for tools. This compact detector can be easily angled and height-adjusted to suit any press configuration. Plus, it’s the only detector that features an electrical powered lift.
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Intertek Group plc
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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TeraSolve -
TeraView Ltd
This module is an addition to the TeraPulse LX product-range. It has been optimized for non- destructive determination of the disintegration and dissolution performance of finished pharmaceutical tablets and other solid dosage forms.
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Loma Systems
The Insight PH Pharmaceutical Metal Detector is designed for inspecting tablets and capsules after the tablet and de-duster process with throughput of up to 30,000 units per minute. The system is built with a gas strut stand frame offering exceptional manoeuvrability making it convenient for use with all leading tablet presses and encapsulation machines.Designed with throughput of up to 30,000 units per minute, the Insight PH comes complete with full IQ, OQ & PQ validation documents and certification.
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ViTec Co. Ltd
The automated system for identifying pharmaceutical codes includes two scanners of the pharmaceutical code, two sensors for the presence of an object and a data processing unit (BOD). When the box or instructions are passed under the object presence sensors, the farm code is read by the corresponding scanner and the results are transmitted to the computer via the Ethernet interface. The BOD verifies the correctness of the read out farm code by comparing this code with the reference farm code set at the beginning of the system operation. If the farm code has not been read or does not match the standard, the packaging machine stops and the type of error is displayed on the indicators.
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Loma Systems
The Insight Pharmaceutical Vertical Fall Metal Detection system is designed for inspecting powders and granules with a throughput of up to 3000kg per hour.
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Pharmaceutical Elemental Impurities Analysis System -
Shimadzu Corp.
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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MRC ltd.
It provides outstanding stability testing performance for manufacturers of pharmaceuticals, cosmetics, food, and personal care products.