青云翻译

So the approval process, resulting in the increased longevity of business investment, and increased risk of new enterprises of the production of Class III medical devices manufacturers license is required to the provincial food and drug regulatory Board to apply the product to the national drug Supe

So of approval program, led to enterprise investment cycle elongated, risk increased, especially production third class medical instruments of new Office Enterprise, production enterprise license be to provincial food drug regulatory authority bid, and products to to national drug prison Council app

The like this examination and approval procedure, causes the enterprise to invest the cycle to elongate, the risk enlarge, produces the third kind of medical instrument to manage the enterprise newly in particular, the production enterprise permit must apply for to the provincial level food drugs su

So the approval process, resulting in longer investment cycles, increased risks, particularly for the Production category 3 medical equipment in the new enterprises, the production company license required to be submitted to the provincial food and drug regulatory authority, and the product you want

So of approval program, led to enterprise investment cycle elongated, risk increased, especially production third class medical instruments of new Office Enterprise, production enterprise license be to provincial food drug regulatory authority bid, and products to to national drug prison Council app