Learn key principles of cleanroom design to support contamination control and meet GMP requirements in pharmaceutical manufacturing.

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 ...

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 ...

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, ...

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 ...

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 ...

VOLTAS announces that clean room space within its new facility is now available for medical device startups to rent for product development and manufacturing. There has to be a place where ten or more ...