Measures Tablet Hardness, Thickness, and Diameter

The TBH 425 Series from ERWEKA is a versatile, semi-automatic tablet hardness tester designed for pharmaceutical, nutraceutical, and R&D applications. Specializing in precise measurement of tablet hardness, thickness, and diameter, the series includes models like TBH 425, TBH 425 D, TD, and WTD to cater to diverse testing needs. The TBH 425 allows up to 10 samples to be tested in its compact star feeder system, ensuring efficient quality control. With automated transportation and measurement, it supports standard and custom testing routines with programmable tolerance settings. It integrates easily into lab operations, connecting via USB for easy data transfer to external systems, ensuring compliance with 21 CFR 11 standards. Optional integration with external analytical balances enhances measurement accuracy, while the AutoCal 2.0 system simplifies calibration. Capable of handling various tablet shapes and sizes, this series is essential for maintaining rigorous quality standards in laboratories dedicated to tablet production.

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Mixes and Blends Pharmaceutical Powders and Granules

The Cube Mixer KB Series from ERWEKA GmbH offers versatile mixing solutions for pharmaceutical and chemical industries, facilitating batch operations with reliability. Its unique tumbling action, enhanced by three strategically positioned stainless steel rods, ensures a homogenous blend of powders and granules. Available in multiple versions, including acrylic glass (KB 15 and KB 20) and stainless steel (KB 20 S), the mixer caters to diverse material compatibility needs. It employs the ERWEKA Universal Gear UG, allowing operation at various angles for optimal efficiency. Ideal for producing paracetamol powder, multivitamin tablets, and fine chemicals, this series supports compliance with industry standards while offering customizable options for specific production demands.

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Mixes Pharmaceutical Powders and Granules

The Double Cone Mixer DKM from ERWEKA GmbH is a high-efficiency solution designed for the precise mixing of pharmaceutical powders, granules, and fine chemicals. By employing a unique multi-dimensional mixing process, facilitated through its angle-adjustable universal gear UG, this mixer achieves uniform blends essential for tablet formulations and nutritional supplements. The DKM can manage a working capacity of up to 5.95 liters within its 11.9-liter stainless steel vessel, making it ideal for batch operations in R&D and processing departments. The manual, bench-top design ensures versatility, while compatibility with various upstream and downstream equipment enhances integration into your production line. Its robust stainless-steel construction offers excellent corrosion resistance, meeting stringent GMP standards. Easy disassembly and smooth surfaces simplify cleaning and maintenance, minimizing downtime between production cycles. For precise mixing applications, the DKM also allows for customization based on specific operational requirements, supported by ERWEKA’s engineering expertise.

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Automates Tablet Hardness and Dimensional Testing

The EasyCheck from ERWEKA GmbH is a fully automated tablet hardness tester, designed to streamline quality control in pharmaceutical and supplement production. It excels with its integrated load cell for accurate weight measurements and Oblong Slider technology for precise alignment of oblong tablets, ensuring consistent width, length, and hardness assessments. Users can effortlessly store up to 100 test methods, managing a staggering 1 million test results on the unit, while benefiting from paperless audit trails and data exports in CSV and XML formats. The compact, user-friendly design integrates seamlessly into laboratories, optimizing workflow with its intuitive touch display and USB keyboard support for data input. Built with a robust star-shaped rotary magazine, it accommodates 20 samples, providing full visual inspection capability. The EasyCheck is 21 CFR Part 11 compliant, meeting rigorous pharmacopeial standards, and is ideal for processing applications in pharmaceutical and biotech industries, including aspirins, multivitamin supplements, and herbal tablets. With options for extensive calibration and maintenance ease, it promises advanced functionality and high user convenience.

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Automates Tapped Density Testing for Powders

The SVM II Tapped Density Tester from ERWEKA GmbH revolutionizes density testing for pharmaceutical and chemical powders. What sets the SVM II apart is its cutting-edge SwitchPlate system, offering unprecedented adaptability with five interchangeable configurations for USP methods 1, 2, and 3. This tabletop device excels in precision by integrating the TestAssist feature, which guides you through testing and automatically calculates crucial metrics like the Hausner Ratio and Compressibility Index. It’s perfectly suited for ensuring product consistency in pharmaceutical tablets and the accurate formulation of metal powders, pigments, and fillers. With a focus on ease of use, the intuitive 7-inch touch display enhances operator efficiency in laboratory and R&D settings. Meeting USP, ASTM, and DIN standards, the SVM II ensures compliance and reliability, making it an indispensable tool in quality control laboratories. Its noise reduction capabilities and future-proof upgrade options further underscore its suitability for rigorous testing environments.

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Conducts High-Volume Dissolution Testing for Tablets

The DT 9510 Series from ERWEKA is a cutting-edge digital dissolution tester designed to streamline high-volume pharmaceutical analysis. Featuring up to 14 test stations powered by a single motor, it ensures uniform and precise dissolution testing, compliant with USP methods 1, 2, 5, and 6. The integrated AirLift system offers safe, ergonomic manipulation of the dissolution head, enhancing operator control during batch testing. This equipment is highly versatile, suitable for a range of products including aspirin tablets and biotin gummies.

Engineered with an embedded-PC, the DT 9510 offers modern user interface capabilities, including TestAssist for optimally guided tests and network printing for seamless data documentation. Its robust design accommodates future upgrades, allowing laboratories to transition from manual to semi-automatic or fully integrated online systems, complete with automatic sampling and temperature control. The water bath maintains stability with minimal evaporation, while the external flow-through heater minimizes vibrations during operation. The DT 9510 is engineered with durability in mind, featuring a one-piece moulded PET water bath and easy-clean interfaces, and it is 100% compliant with USP, EP, and JP standards, assuring rigorous validation processes are met.

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Simulates Gastrointestinal pH Conditions for Tablet Dissolution

The BioDis RRT 10 from ERWEKA is a precision dissolution tester designed for the pharmaceutical and biotech industries, specializing in the analysis of extended and sustained release dosage forms. This equipment is distinguished by its capability to precisely simulate the varying pH conditions of the human gastrointestinal tract, facilitating accurate testing and profiling of tablets, coated tablets, and nutraceuticals. Featuring an external flow-through heater, it ensures minimal vibration and a constant temperature, enhancing test consistency. The modular system operates with adjustable speeds and includes an automated sample transport mechanism for seamless testing across various media pH zones. Its compliance with USP, EP, and JP standards makes it ideal for R&D and quality control environments focused on meeting strict regulatory requirements. With the option for configurations involving USP methods 3 and 7, and customizable vessel sizes ranging from 50 ml to 1000 ml, the BioDis RRT 10 offers the flexibility to meet diverse testing needs. A user-friendly touch display and automated vessel cover system reduce media evaporation and simplify operation and maintenance, making it a versatile solution for modern laboratories.

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Performs Manual Disintegration Testing of Tablets and Capsules

The ZT 121 Light Manual Disintegration Tester from ERWEKA is a compact and efficient solution for quality control in pharmaceutical and biotech labs. With its easy-to-use membrane keypad and dual LED display, you can precisely set and monitor test parameters such as run time and bath temperature. This tester is fully compliant with USP, EP, and JP standards, ensuring reliable testing of tablets, capsules, and other solid dosage forms. The unit’s manual operation with a single motor-driven test station is designed for bench-top use, making it ideal for research and development departments. Its integrated flow-through heating system maintains water bath accuracy to ±0.2°C, supporting temperature-sensitive operations. Options for qualification documents, maintenance services, and water stabilizers are available, ensuring seamless integration into your existing quality assurance protocols.

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Measures Suppository Softening Time

The Suppository Penetration Tester PM 30 from ERWEKA GmbH is designed to accurately measure the softening time of suppositories, an essential parameter for ensuring proper drug release and efficacy. This equipment excels with its simple yet effective visual observation capabilities, accommodating up to three test stations for concurrent analysis. Suitable for pharmaceutical applications, it evaluates glycerin, cocoa butter, paracetamol, ibuprofen, laxative, and antifungal suppositories. Operating as a bench-top manual device, it integrates seamlessly into laboratory and R&D settings. The PM 30 is compliant with EP methods, supported by options like glass test tubes and immersion thermometers, ensuring both precision and adaptability in quality control processes.

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Measures Suppository Hardness Accurately

The SBT 2 Suppository Hardness Tester from ERWEKA GmbH is a precision instrument designed for pharmaceutical manufacturers and quality control laboratories. This bench-top machine features an electrically heated chamber with interchangeable inserts to accommodate diverse suppository sizes. It assesses mechanical strength by incrementally applying weights until collapse, offering critical insights into formulation consistency. This allows precise quality control for products such as analgesics and antifungal suppositories. Despite its manual operation, the device integrates seamlessly into R&D and QC setups, providing reliable performance across various pharmaceutical and biotech applications. Optional customization ensures compatibility with specific testing protocols and regulatory compliance.

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