product registration

Responsible for documentation preparation of product registration; Ensure the document compliant with China regulation requirement.

If the products have not been granted product registration, they should be exported from Vietnam.

Ensure all accurate data is recorded and complete clinical trial in a timely manner to support product registration.

Some might call you if you filled out a product registration card.

Track new government regulations to review and update policies, process and planning to support product registration.

the state shall implement a product registration system for manufacturing medical devices.

Responsible for timely local product registration of products from Shanghai facility.

Cooperating with other Dept to finish new product registration.

Be responsible for product registration.

Preparing product registration submissions, tracking the process based on Registration Plan.

Activation is separate from product registration, which is optional.

Copy of lastest Certificate of Product Registration.

Notice of Beijing Municipality on the Work of Software Enterprise Determination and Software Product Registration

Management Measure on Xiamen Software Enterprises authentication and software Product Registration

Familiar with the rules and regulations of pharmaceutical advertising and medical product registration;

responsible for documentation preparation of product registration;

Test report on product registration given by medical device inspection institutions (applicable to Class II and Class III medical device)

To register your product and for help with product registration issues, visit the following Microsoft Web site

Look for the product registration email we sent to you

To offer technical support for product registration and other related matters

API and drug product registration and GMP compliance DMF cGMP