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First Name

Last Name

Phone Number

Address Line 1

Address Line 2

City

State

Zip Code

Country

Required Service

Enter details related to "Regulatory Affairs"

Name of the device

Intended Use of the Device

Country of Origin

Country of origin approval

Yes

Under Review

Name and address of the Manufacturer (Legal Manufacturer)

Address Line 1

Address Line 2

City

State

Zip Code

Country

Enter details related to "Quality Management System"

What is your product line/type of device?

What is the size of your company?

What stage of product development are you in?

Specify the stage of product development

Do you have any existing QMS established?

Please specify

Enter details related to "Clinical Trials"

Name and intended use of the device?

Is it a First in human study?

Yes

In which countries did you conduct the studies?

What is the proposed sample size for this study?

Proposed number of study sites?

Enter details related to "Training"

What training are you interested in?

Please specify

How many participants will be joining along with you?

Timeline for the training - Tentative Dates

Any specific aspects of the standard you wish you focus on?

Your Message

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