I will fda medical device labeling and packaging compliance

Are you planning to market a medical device in the US, European Union, Switzerland, Australia or another international market?

I provide regulatory review and research support for medical device labeling, packaging and UDI requirements based on your device and target market.

Services may include:

Medical device label and packaging review

Country specific labeling requirements

UDI requirements and implementation support

US FDA labeling and GUDID requirements

EU MDR labeling and UDI requirements

Switzerland medical device labeling requirements

Australia medical device labeling research

Symbols, manufacturer and representative information

IFU and packaging requirements

Regulatory change and requirement research

Multi market labeling comparison

Identification of labeling updates needed for a target market

My background includes hands on experience with medical device quality and regulatory activities, including labeling, UDI, GUDID, EUDAMED, international regulatory requirements and regulatory change support.

Please contact me before ordering with your device type, classification and target market so I can confirm the appropriate scope.