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Medical Container Articles & Analysis

6 articles found

Medical Device Biocompatibility Testing

Medical Device Biocompatibility Testing

Medical device biocompatibility testing is a quality control standard for the development and manufacturing of medical devices. ...

ByProregulations


What Material Is PP Plastic?

What Material Is PP Plastic?

Due to these properties, PP is widely used in a variety of applications, including but not limited to packaging materials, fibers, containers, furniture, medical devices, automotive parts, etc. Its thermoplastic properties also allow PP to be shaped through various processing methods, such as blow molding, injection molding, etc., to meet the needs of different ...

ByXicheng EP (VN) Ltd


Runny or stuffy nose in children. What to do?

Runny or stuffy nose in children. What to do?

When the disease becomes severe and chronic, medications (including antibiotics) often cannot be avoided anymore! You need to remember that there are a lot of risk factors that predispose children to develop an adverse reaction to a medicine. ...

ByNosiboo


New Demand for Medical Devices also Increases Interest in Durable PTFE Products

New Demand for Medical Devices also Increases Interest in Durable PTFE Products

Close to the core of medical device performance are PTFE tubing and FEP sheets, both of which offers a huge array of medical sector applications. ...

ByFluorostore


Why Vaccines should be Refrigerated

Why Vaccines should be Refrigerated

Each vaccine needs to be stored in a cool and refrigerated place to ensure its efficiency and effectiveness are maintained during use. Every year, millions of people are vaccinated to strengthen their immunity and protect themselves from infectious diseases. According to the regulations of the World Health Organization (WHO), vaccination is an approved tool for dealing with deadly contagious ...

ByAKCP


FDA revises cGMP and labeling regulations of medical gases

FDA revises cGMP and labeling regulations of medical gases

Abstract: The US FDA recently amended its cGMP and labeling regulations for medical gases. The chief impetus for modifying the regulation was the number of injuries and deaths where medical gas containers carrying gases other than oxygen were falsely connected to a healthcare’s facility oxygen supply system. FDA in the Federal Register ...

ByComplianceOnline

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