国家外汇管理局


关于外商投资企业在境内以外币计价结算的管理规定(附英文)

1989年1月7日，国家外汇管理局

为促进利用外资事业的发展，加强对外商投资企业在境内以外币计价结算的管理，维护金融秩序的稳定，协助外商投资企业平衡外汇收支，根据《对侨资企业、外资企业、中外合资经营企业外汇管理施行细则》和有关规定，特作如下规定：
一、凡外商投资企业（以下简称企业）在境内以外币计价结算销售产品的，须向企业所在地的国家外汇管理局或其分、支局（以下简称外汇管理部门）提出申请。
二、凡符合下列条件之一的企业，可向外汇管理部门申请以外币计价结算销售其产品：
1．企业生产的产品属国家计划内需要进口的商品；
2．企业向经济特区、经济技术开发区或外商投资企业销售其产品；
3．企业生产的产品属于国内生产企业需要用外汇进口的原材料和零配件。
三、企业申请在境内以外币计价结算销售其产品时，应向外汇管理部门提供下列文件：
1．在境内以外币计价结算销售产品的申请报告。报告中应写明理由、产品名称、数量、金额、期限等内容；
2．在我国登记注册的会计师事务所出具的企业如期缴足资本的验资证明；
3．外汇管理部门要求提供的其他文件。
四、外汇管理部门按年度审批企业的申请，应对企业以外币计价结算销售其产品的金额、数量、品名、期限作出规定，并核定企业以外币计价销售产品的年度数额。
五、凡属需在异地以外币计价结算销售产品的，收取外币的企业所在地外汇管理部门批准后，抄送各有关分局，并报总局备案。
六、凡经批准以外币计价结算的产品，其价格一般应参考同类出口商品的离岸价或同类进口商品的到岸价，同质同价，优质优价。＃13七、凡属下列情况者，一般不得以外币计价结算销售其产品：
1．企业违反合同、章程或批准文件，不履行外销或返销责任，不按期达到国产化程度的；
2．属国家不鼓励投资的企业或产品。
八、未经外汇管理部门批准，企业不得以外币计价结算销售其产品。企业违反本规定，外汇管理部门根据《违反外汇管理处罚施行细则》，予以处罚。
九、本规定公布之前的有关办法，与本规定有抵触的，以本办法为准。
十、本规定解释权属国家外汇管理局。
十一、本办法自一九八九年三月一日起实行。

PROVISIONS GOVERNING THE USE OF FOREIGN CURRENCY BY FOREIGNINVESTED ENTERPRISES IN COMPUTING PRICES AND SETTLING ACCOUNTS WITHINCHINA

(Promulgated on March 1, 1989)

Whole Doc.
The following Provisions are enacted by the State Administration of
Exchange Control (SAEC) in accordance with the Rules for the
Implementation of Foreign Exchange Controls Relating to Overseas Chinese
Enterprises, Foreign Enterprises and Chinese-Foreign Joint Ventures and
relevant regulations with a view to facilitating the use of foreign
capital, tightening control over the use of foreign currency by
foreign-invested enterprises in computing prices and settling accounts
within China, and helping these enterprises balance their foreign exchange
receipts and expenditures:
Article 1
A foreign-invested enterprise (hereinafter referred to as enterprise)
that wishes to use foreign currency to compute prices and settle accounts
for the products it sells in China must apply to the SAEC or its branch or
sub-branch office (hereinafter referred to as exchange control
authorities) in the place where the enterprise is located.
Article 2
The applicant must conform to one of the following conditions:
(1) Its products are those that need to be imported under the State
plan;
(2) Its products are sold to the special economic zones,
economic-technological development zones, or foreign-funded enterprises;
or
(3) Its products are raw or semi-finished materials, spare parts or
fittings which domestic production enterprises need to import with foreign
exchange.
Article 3
While applying for the use of foreign currency to compute prices and
settle accounts for the products it sells in China, the enterprise shall
submit the following documents to the exchange control authorities:
(1) An application to that effect, stating the reason for
application, the names and amounts of products, the sum of money, and the
duration;
(2) A certificate from an accountant office registered in China
confirming that the enterprise's capital has been fully paid up as
scheduled; and
(3) Other documents required by the exchange control authorities.
Article 4
The exchange control authorities shall examine and approve the
application from an enterprise on an annual basis, stipulating the sum of
money, the amounts and names of products, the time limit for the use of
foreign currency by the enterprise in computing prices and settling
accounts for its products, as well as the annual quota for the products
involved in this regard.
Article 5
In case an enterprise needs to use foreign currency to compute prices
and settle accounts for the products it sells in places other than where
it is located, it must obtain approval from the exchange control
authorities at the place where the enterprise receiving the foreign
exchange is located, and copies of the document of approval shall be sent
to the relevant SAEC branch offices and reported to the SAEC headquarters
for reference.
Article 6
For products the prices of which are allowed to be computed and the
accounts to be settled in foreign currency, the prices shall generally be
set with reference to the FOB prices of the same category of export goods
or the CIF prices of the same category of import goods, according to the
principle of the same prices for goods of the same quality and higher
prices for goods of higher quality.
Article 7
Generally, an enterprise shall not be allowed to compute prices or
settle accounts in foreign currency for its products in one of the
following cases:
(1) If the enterprise, in violation of the provisions of its
contracts, articles of association or the documents of approval, has
failed to perform its duties in exporting its products or selling them in
China, or failed to reach the goal of switching to domestic materials and
parts in manufacturing the products; or
(2) If the enterprise or its products are not of the category in
which investment is encouraged by the State.
Article 8
Without the approval of the exchange control authorities, no
enterprise may use foreign currency to compute prices and settle accounts
for its products. Any enterprise violating these Provisions shall be
punished by the said authorities in accordance with the Rules for the
Implementation of Penalty on Offenses Against Exchange Control.
Article 9
In case of conflict between past provisions and the present
Provisions, the present Provisions shall prevail.
Article 10
The right to interpret these Provisions resides in the SAEC.
Article 11
These Provisions shall come into effect on March 1, 1989.


国家食品药品监督管理局


关于进一步加强抗震救灾捐赠药品和医疗器械监管工作的通知

国食药监电[2010]7号


各省、自治区、直辖市食品药品监督管理局（药品监督管理局）：

　　为切实做好青海玉树地区抗震救灾期间药品、医疗器械监管工作，确保捐赠药品、医疗器械质量安全，根据《关于加强捐赠救灾药品和医疗器械监管工作的通知》（国食药监电〔2008〕20号）精神，现就有关事项通知如下：

　　一、各省（区、市）药品监督管理部门要高度重视抗震救灾捐赠的药品和医疗器械的监督管理工作，密切关注并引导辖区内企业向地震灾区捐赠所需的药品和医疗器械产品，加大对企业捐向灾区的药品和医疗器械的监管和检查力度，强化捐赠人对捐赠的药品、医疗器械的质量安全责任意识。

　　二、捐赠境内生产的药品，必须是经国家局批准生产、获得批准文号且符合质量标准的品种，有效期距失效日期必须在6个月以上；捐赠境内生产的医疗器械应是经食品药品监督管理部门批准生产，获得《医疗器械注册证》且符合质量标准的产品，其中，一次性使用无菌医疗器械有效期限距失效期必须6个月以上。

　　三、捐赠境外生产的药品，应是我国药品标准收载或我国已批准注册的品种，以及国际上通用药典收载、在注册国合法生产并上市且符合质量标准的品种。捐赠境外生产的医疗器械应为已获得我国《医疗器械注册证》或已经外国政府部门批准上市且质量合格的产品。

　　四、地震灾区省级食品药品监督管理部门应及时掌握受赠产品的清单（包括：名称、剂型、规格、数量、生产批号、有效期、生产单位、进口口岸等），做好对受赠药品、医疗器械的质量验收、检验、分发、记录等工作。

　　五、加大对违法行为的查处力度,对捐赠的药品和医疗器械存在假冒伪劣、过期失效等违法情形的，要依法从重查处。


　　　　　　　　　　　　　　　　　　　　　　　　　　　　国家食品药品监督管理局
　　　　　　　　　　　　　　　　　　　　　　　　　　　　 二〇一〇年四月十五日