Chromservis has released new upcoming dimensions of ASTRA® C18-Hybrid columns. Column description Part No. Columns with 3µm particles ASTRA® C18-HYBRID HPLC column, 3,0 µm 100 mm × 3,0 mm AST-6016-II30 ASTRA® C18-HYBRID HPLC column, 3,0 µm 150 mm × 3,0 mm AST-6016-IK30 ASTRA® C18-HYBRID HPLC column, 3,0 µm 50 mm × 4,6 mm AST-6016-IG46 ASTRA® C18-HYBRID HPLC column, 3,0 µm 100 mm × 4,6 mm AST-6016-II46 ASTRA® C18-HYBRID HPLC column, 3,0 µm 150 mm × 4,6 mm AST-6016-IK46 ASTRA®

PTWS 830 is an 8-position, compact tablet dissolution testing instrument for solid dosage forms as described in USP chapter <711/724> and EP section<2.9.3/4> as well as the BP, DAB and Japanese Pharmacopeia section <15>. Integrated audit trail ensures 21 CFR Part 11 regulatory compliance Flexible user management system with unlimited number of users ensures secure access The modern user interface is easy to use and quick to learn MonoShaft™ stirring tool design avoids re-adju

The PT-LT100 leak tester is employed to assess the integrity of packed strips, blisters, and small sachets containing tablets, granules, liquids, and more. This device evaluates the quality of the packaging process and verifies that the seals around the product are completely intact. The PT-LT100 is crafted to detect the tiniest holes and flaws in blister packs and other semi-rigid product packaging. It fully adheres to the current USP <1146> monograph. Leak testing is extens

The Pharmag Pilot Plant System is designed for specialised uses such as developing new products, transitioning from testing to small-scale production, and creating specialty materials that are not typically produced in large volumes. This type of equipment is well-suited for both the fine chemical and cosmetics sectors, as well as the pharmaceutical industry. The Pharmag range is also widely used in Pharmacy teaching departments at universities and for producing low-volume, s

The CAMAG CBS 119 publication, showcases HPTLC as a fast and simple solution for the analysis of Cannabis, especially in regard to different analytical goals. In a limit test numerous samples can be assessed in parallel as to their classification as narcotic drug. Detection and a precise assay of individual cannabinoids is also possible. https://camag.com/login/?redirect_to=/article/quantification-of-tetrahydrocannabinol-in-cannabis-sativa/

Introduction to the PTB 500 NICE Tablet Testing System The PTB 500 NICE semi-automated tablet testing system is a robust instrument designed for precise measurement. It assesses five key parameters of a sample: hardness, diameter (or length), thickness, width, and tablet weight. This system includes an integrated analytical balance and a sample carousel. It adheres strictly to the EP <2.9.8> and USP <1217> Pharmacopoeia standards. Features of the PTB 500 NICE The PTB 500 NICE

PTWS 130 is a 6-position, compact tablet dissolution testing instrument for solid dosage forms as described in USP chapter <711/724> and EP section<2.9.3/4> as well as the BP, DAB and Japanese Pharmacopeia section <15>. The S-Variant offers independent stirrer speed control for each of the six testing stations. Each package includes a complete set of USP vessels, stirrer shafts, and USP apparatus 2 paddles, ensuring compliance with regulatory standards and facilitating effici

A big thanks the Aphex Pharma solutions who gave us the opportunity to sponsor and attend the 3rd Pharmaceutical Development Conference and Exhibition in Melbourne 1st September 2026. We all look forward to meeting you in Melebourne.

To ensure that an HPLC or UHPLC system operates optimally, it is crucial to use dependable replacement parts that fit correctly, seal reliably, and facilitate precise analytical outcomes. Optimize Technologies offers replacement components for a variety of liquid chromatography instruments, including those from Agilent/HP, Waters, Shimadzu, Thermo, Dionex, Varian, Jasco, Hitachi/Merck, and other leading manufacturers. Our replacement parts are designed for laboratories requir

Developing and optimising pharmaceutical processes necessitates a thorough understanding of reaction kinetics to enhance efficiency, manage impurities, and ensure reliable scale-up. However, obtaining high-quality kinetic data is challenging due to limitations in many laboratory platforms, especially in achieving representative mixing, precise temperature control, and consistent sampling. The ReactALL™ workstation was developed to fill this gap by providing automated, medium-

Explore the newest addition to the HPTLC Association’s Method Collection, which now includes more than 300 methods designed for a range of applications: Identification of herbal drugs and their preparations Identification of substance classes Identification of complex mixtures All methods comply with the Association’s HPTLC Standard Operating Procedure. Many of these methods, or their improved versions, have been included in the monographs for herbal drugs and dietary supplem

Introducing NEW ASTRA® Hybrid HPLC Columns – Next Generation Performance for Demanding Application Hybrid silica combines the strength of inorganic silica with the flexibility of organic chemistry, resulting in a material designed for exceptional performance. Its improved durability and optimized surface properties make hybrid silica ideal for more intelligent and enduring solutions in advanced industrial and technological fields. The combination of high-density end-capping a

The World Health Organization (WHO) estimates that 50% of the medications sold online are fake. To combat drug falsification, the Sanofi group established a distinctive laboratory in 2008, employing various analytical techniques such as HPTLC. In CAMAG's CBS the article "HPTLC detection of falsification in drugs" was published, the article showcased rapid parallel screening of many samples. Which included up to 10 samples analysed in less than one hour. The developed method i

Crystallisation in Electronics R&D In the fast-paced electronics industry, precision and innovation are key to success. The drive to create electronics that are flexible, intelligent, and sustainable presents new challenges. Crystallisation is crucial in providing solutions. Technobis offers cutting-edge crystallisation technology to achieve unmatched efficiency and reliability in the production and research of electronic materials. Technobis has released a booklet that delve

CAMAG's latest HPTLC application note introduces a complete HPTLC-umuC bioassay workflow for the rapid detection and localization of genotoxic compounds directly on the chromatographic plate.

X-ray quality single crystals must exhibit a high degree of internal order, as evidenced by an X-ray diffraction pattern, and should measure between 0.1 - 0.4 mm in at least two of the three dimensions. The CrystalBreeder assists you in setting up parallel crystallization experiments under various conditions, maximizing your chances of success in a relatively short time. To grow single crystals, avoid solvents where your compound forms supersaturated solutions, as excessive n

The Importance of Automation in Crystallisation Automation goes beyond being just a trend; it significantly boosts throughput, reproducibility, and data quality, while minimizing manual work and associated risks. By incorporating our crystallisation platforms into automated processes, you can efficiently conduct solubility screening, particle engineering, solid-form studies, and other tasks with little human involvement. Technobis software and hardware are built from the grou

During this webinar, the guest speaker Jude Eames from Eurofins CDMO Alphora will present a case study on polymorphic impurities in the development of pharmaceutical processes. Controlling Polymorphic Impurities in Pharmaceutical Processes About the Webinar In this webinar, guest speaker Jude Eames from Eurofins CDMO Alphora will share a case study on polymorphic impurities in pharmaceutical process development. The case study highlights the importance of understanding polymo

The new Pharma Test 2026 brochure which includes all the latest instruments and innovations for Dissolution Testing and Galenic Instruments.

CAMAG's CBS 136 | Article 2 (2026), This article introduces a universal HPTLC method capable of simultaneously separating fourteen antimalarial active pharmaceutical ingredients along with three related impurities on a single plate. This method is ideal as a rapid screening tool for pharmaceutical quality control, particularly in settings with limited resources.