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Confidential Information JMS Validation SummaryRevision number:1Page 2 of 18TABLE OF CONTENTS 1.0 ISO 10993 & USP/ EUROPEAN PHARMACOPEIA. 1.1 ISO 10993 Compliance. 1.1.1 Hemolysis Human Blood ISO
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Start by opening the JMS Flex Film Validation form.
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Enter your personal information such as name, address, and contact details.
03
Provide the necessary details about the flex film product you want to validate, including its specifications and manufacturing details.
04
Attach any supporting documents or certificates related to the flex film product.
05
Double-check all the information provided to ensure accuracy and completeness.
06
Submit the form by clicking on the 'Submit' button.
07
Wait for the validation process to be completed, which may take some time depending on the complexity of the flex film product.
08
Once the validation is done, you will receive a confirmation or rejection notification regarding the flex film product.

Who needs jms flex film validation?

01
Manufacturers and suppliers of flex film products.
02
Regulatory authorities overseeing the production and distribution of flex films.
03
Customers or end-users of flex film products who want to ensure their quality and conformity to standards.
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JMS flex film validation is a process to validate the usage of flexible films in packaging.
Manufacturers and companies using flexible films in packaging are required to file JMS flex film validation.
JMS flex film validation can be filled out online through the designated portal provided by the regulatory authorities.
The purpose of JMS flex film validation is to ensure compliance with regulations related to the usage of flexible films in packaging.
Information such as the type of flexible film used, quantity, usage details, and recycling/disposal methods must be reported on JMS flex film validation.
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