ISO 5628 Guide with Bending Stiffness Testing Machine Insights The bending stiffness test is a critical material property evaluation method used across industries including packaging, medical devices, pharmaceuticals, textiles, and paperboard production. This test measures a material’s resistance to bending and provides insights into its rigidity, flexibility, and structural performance. ISO 5628:2019 outlines standardized principles for executing such tests using two-point, three-point, or four-point bending methods. To ensure accurate results, manufacturers and quality control professionals must follow the correct procedures, use compliant equipment, and understand how variables like material thickness, modulus of elasticity, and support conditions affect results. This article guides you through the proper execution of the bending stiffness […]

Introduction: Why a Tablet Hardness Tester Is Essential In the pharmaceutical industry, ensuring consistent tablet quality is critical for patient safety and regulatory compliance. A tablet hardness tester plays a central role in this process by measuring the mechanical integrity of solid oral dosage forms. This test allows manufacturers to confirm that tablets can endure mechanical stresses during manufacturing, transportation, and use without compromising their performance. Cell Instruments provides advanced testing solutions, including the MPT-02 Tablet Hardness Tester, designed for high-precision, efficient testing in both R&D and quality control environments. Understanding Tablet Hardness Test and Related Measurements Evaluating tablet hardness is more than just applying pressure until a tablet breaks.

Introduction to ISO 9187-1 for Ampoules ISO 9187 is a critical international standard that specifies the technical and performance requirements for glass ampoules used in medical injectables. The standard ensures that ampoules are safe, reliable, and suitable for containing sterile pharmaceutical products. It primarily applies to ampoules made of glass and focuses on key properties such as hydrolytic resistance, annealing quality, and the breaking force required to open the ampoule cleanly and safely. In medical and pharmaceutical settings, ampoules must maintain sterility while being easy to open without causing glass shards or user injury. Hence, accurate breaking force measurement for glass ampoules is essential, and ISO 9187-1 provides the precise

How to Test Compression Strength: A Practical Guide to Ensuring Packaging Integrity and Durability In modern packaging design, understanding how to test compression strength is essential for product protection, supply chain reliability, and regulatory compliance. Whether dealing with infusion bags, plastic packaging, or medical containers, ensuring that packaging can withstand external pressure is a key component of functional safety and product integrity. At Cell Instruments Co., Ltd., we specialize in high-precision, standard-compliant equipment that enables packaging engineers and quality professionals to carry out reliable compression tests. This article outlines how compression strength testing works, how it ensures packaging integrity, and how the right instrumentation makes all the difference. Why Compression

Syringeability Test Syringe Functionality Testing Item The syringeability test is an essential quality assurance method used to evaluate the ease and consistency with which a syringe delivers its contents. In pharmaceutical, medical device, and packaging industries, this test plays a crucial role in verifying the safety, effectiveness, and user-friendliness of syringes and injectables. It is especially significant in ensuring that syringes meet regulatory and functional standards for clinical use. At Cell Instruments Co., Ltd., we specialize in developing advanced testing equipment, including our MST-01 Medical Syringe Tester, to support manufacturers and quality control professionals in accurately conducting syringeability and related tests. Understanding Syringeability and Injectability The terms syringeability and injectability

リークテスト装置USP 1207 パッケージの完全性評価パッケージの世界、特に医薬品、食品、医療機器業界では、製品容器の完全性を維持することが最も重要です。リークテスト装置は、パッケージが厳格な品質基準と規制要件を満たしていることを確認するために使用される重要なツールです。見積もりを取得リークテスト装置とは？リークテスト装置は、パッケージ、容器、その他の密封された製品の漏れや完全性の侵害を検出するために使用される特殊な装置です。これらの装置は、密封されたアイテムに圧力、真空、またはガス媒体を適用し、圧力の損失やガスの存在を測定することによって機能します。

ソフトゼラチンカプセルの破裂試験 – 品質と製品の完全性を確保 ソフトゼラチンカプセルは、有効成分を効率的に送達できるため、製薬業界や栄養補助食品業界で広く使用されています。これらのカプセルが実際の条件下で完全性を維持していることを確認するために、メーカーはさまざまなテストに依存しています。最も重要なテストの1つは、ソフトゼラチンカプセルの破裂テストです。このテストは、カプセルの強度と破損に対する耐性を確認するのに役立ちます。このテストは、カプセルが摂取時に効果的に機能し、早期に破損しないことを保証する上で重要な役割を果たします。 ソフトゼラチンカプセルの破裂テストの重要性 ソフトゼラチンカプセルは繊細であり、

Mastering the Vacuum Leak Test Procedure ASTM D3078 A Deep Dive into Vacuum Decay Leak Testing Solutions, Apparatus Principles, and ASTM D3078 Compliance Introduction to Vacuum Leak Test Procedures Leak detection is a critical aspect of quality assurance in industries such as pharmaceuticals, food packaging, and medical devices. A reliable vacuum leak test procedure ensures product integrity, safety, and compliance with industry standards. Among the most advanced methods is the vacuum decay leak testing solution, which leverages precise pressure differential measurements to identify even the smallest leaks. Understanding the Vacuum Decay Package Leak Tester A vacuum decay package leak tester is a sophisticated device designed to detect leaks in sealed packages by measuring changes in

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