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Syringeability Test – Syringe Functionality Testing

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Syringeability TestSyringe Functionality Testing Ensuring that a syringe performs reliably during actual use is critical in both clinical and laboratory environments. The syringeability test evaluates a syringe’s ability to deliver its contents smoothly, safely, and consistently. More than a simple flow assessment, it also considers factors such as injection force, obstruction, ease of administration, and […]

ISO 7864 Hypodermic Needle Sharpness Testing

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ISO 7864 Hypodermic Needle Sharpness Testing Introduction Needle sharpness testing is essential for evaluating hypodermic needles, ensuring they meet safety and performance standards during medical use. Guided by ISO 7864, this testing assesses critical needle parameters to confirm compliance and avoid unnecessary pain or tissue damage during injection. In this article, we’ll discuss how to

Penguji Pembengkokan Tiga Titik Ampul - ISO 9187

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Penguji Tekuk Tiga Titik Ampul - ISO 9187 Unduh Katalog Harap aktifkan JavaScript di browser Anda untuk mengisi formulir ini NamaEmail * Perusahaan * WhatsAppPesan * Situs Web Kirim Pesan Pengantar Pengujian Kekuatan Pecah Ampul Ampul farmasi banyak digunakan untuk pengiriman obat steril, yang membutuhkan desain yang tepat dan jaminan kualitas untuk memastikan penggunaan yang aman, efektif, dan sesuai. Ampul

ISO 9187-1

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Ampoule Three Point Bend Test ISO 9187-1 ISO 9187-1 is a critical international standard that defines the requirements for glass ampoules used for injectable medications. Ensuring these ampoules meet the required mechanical and chemical standards is essential for both patient safety and regulatory compliance. This standard outlines specifications for hydrolytic resistance, annealing quality, and most

Uji ketahanan hidrolitik ISO 719

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Glass Hydrolytic Resistance Test ISO 719 Hydrolytic Resistance Test & ISO 719 Sample Preparation for Glass In the world of glass quality control, the hydrolytic resistance test defined by ISO 719 plays a critical role. This hydrolytic test for glass evaluates how much alkali leaches from glass grains when boiled in purified water at 98

LLA Collar Torque Resistance

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LLA Collar Torque Resistance ISO 11040-4 Annex G4 In pharmaceutical manufacturing, ensuring the mechanical integrity of prefilled syringes is critical to product safety and performance. One key factor in this integrity is LLA collar torque resistance, which measures the strength of the Luer lock adaptor (LLA) collar under torque. This property ensures that the collar

Luer Lock Rings Pull-Off Force Test – ISO 11040-4 Annex G3

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Luer Lock Rings Pull-Off Force ISO 11040-4 Annex G3 In the pharmaceutical and medical device industries, the luer lock rings pull-off force is a critical parameter to ensure the reliability and safety of prefilled syringes. Proper testing verifies the secure attachment of the luer lock adaptor (LLA) to prevent accidental detachment during use. Importance of

Luer Cone Breakage Resistance – ISO 11040-4 Annex C2

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Luer Cone Breakage Resistance ISO 11040-4 Annex C2 In syringe manufacturing and quality control, one of the most critical mechanical assessments is the luer cone breakage resistance test. The structural integrity of the syringe front end, especially the luer cone, directly impacts both patient safety and device reliability. To ensure consistent, standardized evaluation, the ISO

Flange Breakage Resistance – ISO 11040-4 Annex C1

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Flange Breakage Resistance ISO 11040-4 Annex C1 Flange breakage resistance is a critical quality attribute in prefilled syringe manufacturing. This test determines the mechanical strength of the syringe barrel’s flange—the portion that must withstand applied forces during clinical use. As healthcare regulations tighten globally, meeting the mechanical performance standards outlined in ISO 11040-4 Annex C1

Syringe Leakage Testing – ISO 11040-4 Annex G2

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Syringe Leakage Testing ISO 11040-4 Annex G2 In the field of pharmaceutical and medical device manufacturing, syringe leakage testing is a critical quality assurance process. It ensures that prefilled syringes maintain sterility and do not leak during transport, storage, or use. To meet stringent regulatory expectations, manufacturers must follow international standards such as ISO 11040-4,

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