Flexibility in a Pharmaceutical Labeling Machine was less needed in the past, If you are finding batch sizes are getting smaller was less need in the past. If you are finding batch sizes are getting smaller, whether from smart drugs or not, then you should consider investing in a labelling system that has been designed …
Cap torque testing has been an integral part of the packaging industry’s quality control program for years. Cap torque testing helps prevent consumer complaints from difficult-to-open products, product leakage or spoilage from loose caps during transportation. Many packaging facilities use small, manual desktop models that are inconsistent and non-repeatable due to outside variables. A manual …
Cap Torque Testing with Vibrac’s Model 2100 Cap Inspector: Benefits and Improvements Read More »
Cap Torque Inspection tool has been an integral part of the packaging industry’s quality control program for years. Cap torque testing helps prevent consumer complaints from difficult-to-open products, product leakage or spoilage from loose caps during transportation. Many packaging facilities use small, manual desktop models that are inconsistent and non-repeatable due to outside variables. A …
What are Precission Test systems? Precision Test systems are advanced technological solutions designed for accurate and reliable testing in various industries, including electronics, aerospace, automotive, and pharmaceuticals. These systems utilize high-precision instruments and software to perform precise measurements, simulations, and evaluations of components, devices, or systems. They are capable of conducting tests with exceptional precision, …
Now Representing Trusted Name in Precision Test Systems.Need Consultation? Read More »
The Inline Piston Filler series is ideally suited for filling a diverse range of products and is equipped with 2, 4, or 6 heads.
Environmental Specialties’ reach-in chambers are finely crafted to satisfy customers’ most stringent, precise conditions for a wide array of research, development, and manufacturing applications. ‘ reach-in chambers are finely crafted to satisfy customers’ most stringent, precise conditions for a wide array of research, development, and manufacturing applications.
Guidance on PDA 468 Validation Processes: Moist-heat sterilization is a widely used method for ensuring the safety and sterility of medical devices and pharmaceutical products. To ensure that these processes are effective, it is essential to validate them through a rigorous testing program. One important standard for validating moist-heat sterilization processes is PDA Technical Report …
PDA 468 Validation of Moist-Heat Sterilization Processes Read More »
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