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Johnson & Johnson said its operating companies take “a variety of approaches” to identify counterfeit products, including product and packaging security steps that help distinguish authentic and counterfeit products. Read More
Devicemakers will need to include in their license applications performance testing data that “clearly demonstrates that the infusion pump can… Read More
The FDA said it would explore whether it has the authority to issue “umbrella regulations” to identify devices that may require additional training or user education beyond the physician labeling currently required. Read More
The Philippines Food and Drug Administration issued a warning that the Johnson & Johnson First Aid To Go Kit includes devices that have not gone through the registration process and are considered counterfeit and unapproved devices. Read More