Pre-classification issue

April 9–10, 2013(2 days)· Ended
Conference
Shanghai, China
In Person

About This Event

Do you have those troubles & risks?

  • Pre-classification issue

Base on the H.S. code, some biopharmaceutical products are involved CCC, and the 3C application need a lot of documention and a very long time which cannot meet the time requirements of CRO’s clinical trial.

  • Timeliness and expiration issue

A repetitious levy based on the value of the biopharmaceutical products happens when exchange repeat between oversea and domestic customers many times.

  • Confidential Issue

Customers or suppliers, unable or unwilling, for the protection of trade secrets reason, to provide ingredient, function, use, composition and other details of the biopharmaceutical products.

  • The heel of achilles

An authorization must be obtained before Import/Export your biopharmaceutical products like reagent, protein and accompany intermediate. A license must to be gained before every shipment. Some Import/Export authorization is unable to obtain due to CRO company's business scope limited.

Top 5 reasons to attend

You can learn the latest trends in CIQ policy for CRO industry!

It’s a great opportunity to network with layer, consultant & more!

To know how to speed up the customs process, save time and cost!

Familiar with the legal clause, prevent the Pre-classification risks!

Familiar with the tax issue about tariff and VAT!

Event ID: e3mlykb

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