Cleanrooms are designated as controlled environments where the levels of airborne particles are carefully regulated. Their construction and utilization are meticulously planned to minimize the ingress ...

Pharmaceutical products are produced to meet strict standards for effectiveness and quality. Every aspect of quality is assessed, taking into account the risks associated with the method of delivery ...

Butler-based MRPC, a contract manufacturer of medical device assemblies and components, has completed a $2 million renovation project at its headquarters. The eight-month project focused on ...

ProMed, a leading contract manufacturer specializing in medical-grade silicone and plastic components, provides comprehensive support for medical device, pharmaceutical, and combination drug-device ...

Collaboration focuses on blood filters, leukoreduction, cleanroom assembly, and disposable medical manufacturing in ISO 7 & ISO 8 cleanrooms. By working with THY Precision (Hong Yang Precision), we ...

What I am about to share with you is a guide to medical device regulatory classification. In this guide, I will provide you with a step-by-step approach for determining how your medical device will be ...

Medtech-focused contract manufacturer Cadence Inc. reports that it is expanding cleanroom capacity at its Staunton, VA, facility. When completed, the cleanroom will measure 5,000 square feet, ...

The Central Drugs Standard Control Organisation (CDSCO) has launched a new risk classification module on the drug regulator's online system for medical devices in order to simplify the regulatory ...

The Central Drugs Standard Control Organisation (CDSCO) has announced risk classification of 187 medical devices pertaining to interventional radiology under Medical Devices Software, under the ...