Regulations for the Inspection of the Good Distribution Practice for Medical Devices and Licensing of Distribution License
2021-01-29
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Article 1
These Regulations are promulgated pursuant to Paragraph 3, Article 24 of the Medical Devices Act (here after referred to as the “Act”).
Article 2
The medical device dealers applying for distribution license of medical devices in accordance with Paragraph 2, Article 24 of the Act (the “Distribution License”), shall submit a completed application to the central competent authority, with relevant documents or materials provided and the required fee paid.
The relevant documents or materials which shall be provided are as follows:
1. The photocopy of the medical device business permits.
2. The master list of Documentation.
3. The quality manual or equivalent documentation.
4. The layout of the site applying for inspection, including the access to areas of operations such as storage areas, goods receipt, dispatch areas and other related workplaces marked.
5. The operation flow charts for product distribution, including outsourced operations.
6. Other relevant documents and materials.
Where a submitted application is incomplete with any of the above documents and materials, the applicant may be notified by the central competent authority to provide the incomplete documents or materials within a time limit; if the applicant fails provide the documents or materials within the time limit, the application will be rejected.
The application form mentioned in Paragraph 1 of this Article shall be completed in Chinese or English; any application document or material that is written in a language other than Chinese or English, shall include a Chinese or English translation thereof.
The relevant documents or materials which shall be provided are as follows:
1. The photocopy of the medical device business permits.
2. The master list of Documentation.
3. The quality manual or equivalent documentation.
4. The layout of the site applying for inspection, including the access to areas of operations such as storage areas, goods receipt, dispatch areas and other related workplaces marked.
5. The operation flow charts for product distribution, including outsourced operations.
6. Other relevant documents and materials.
Where a submitted application is incomplete with any of the above documents and materials, the applicant may be notified by the central competent authority to provide the incomplete documents or materials within a time limit; if the applicant fails provide the documents or materials within the time limit, the application will be rejected.
The application form mentioned in Paragraph 1 of this Article shall be completed in Chinese or English; any application document or material that is written in a language other than Chinese or English, shall include a Chinese or English translation thereof.
Article 3
Upon acceptance of the above application, the central competent authority shall conduct an inspection of the operating locations of the dealer. A Distribution License shall be issued to the dealer upon confirmation of its compliance with the Medical Devices Good Distribution Practice Regulations; If the inspection demonstrated non-compliance results, the dealer may apply for a re-assessment within two (2) months of receipt of a non-compliance notice; however, an application for re-assessment can only be made once.
The medical device dealers who are disagreed with the notice of non-compliance results with the provisions in the preceding paragraph, or whose application for re-assessment by the provisions of the preceding paragraph are rejected, the medical device dealers may initiate an administrative appeal proceeding in accordance with applicable laws.
The medical device dealers who are disagreed with the notice of non-compliance results with the provisions in the preceding paragraph, or whose application for re-assessment by the provisions of the preceding paragraph are rejected, the medical device dealers may initiate an administrative appeal proceeding in accordance with applicable laws.
Article 4
For the Distribution License, the following items shall be specified:
1. The name of the medical device dealer.
2. The address of the medical device dealer.
3. The distribution operation items for which the license has been granted.
4. The storage location(s) of medical devices.
5. The license number.
6. The expiration data.
If there is any change to the specified matters under Subparagraph 1 and 2 of the preceding paragraph, the medical device dealers shall submitted an application form to the central competent authority after paying the application fee, along with the photocopy of the Distribution License and updated the medical device business permits, within thirty (30) days from the date of the occurrence of the change.
The expiration date of the License will not be extended for any change described in the preceding paragraph.
If there is any change to the matters about Subparagraph 3 and 4 of Paragraph 1 of this Article, its application and inspection procedures shall be subject to the requirements specified in the preceding two articles.
1. The name of the medical device dealer.
2. The address of the medical device dealer.
3. The distribution operation items for which the license has been granted.
4. The storage location(s) of medical devices.
5. The license number.
6. The expiration data.
If there is any change to the specified matters under Subparagraph 1 and 2 of the preceding paragraph, the medical device dealers shall submitted an application form to the central competent authority after paying the application fee, along with the photocopy of the Distribution License and updated the medical device business permits, within thirty (30) days from the date of the occurrence of the change.
The expiration date of the License will not be extended for any change described in the preceding paragraph.
If there is any change to the matters about Subparagraph 3 and 4 of Paragraph 1 of this Article, its application and inspection procedures shall be subject to the requirements specified in the preceding two articles.
Article 5
The Distribution License is valid for a period of three (3) years. If an extension thereof is required, an application shall be submitted six (6) to twelve (12) months before the expiration date of the current license. The validity period can be extended for up to three (3) years for each application. The application for an extension of the license and its inspection procedures shall be subject to the requirements specified in Article 2 and Article 3.
If an extension application is submitted within the period prescribed in the preceding paragraph, but the central competent authority fails to make a decision of approval/disapproval there of before the expiration date of the current Distribution License, and such failure is not attributable to the fault of the applicant of medical device dealer. The period of validity of the original license shall be extended to the date on which a decision of approval/disapproval regarding the extension application is made.
If an extension application is submitted within the period prescribed in the preceding paragraph, but the central competent authority fails to make a decision of approval/disapproval there of before the expiration date of the current Distribution License, and such failure is not attributable to the fault of the applicant of medical device dealer. The period of validity of the original license shall be extended to the date on which a decision of approval/disapproval regarding the extension application is made.
Article 6
The central competent authority may conduct an inspection on the operating locations of the medical device dealer irregularly without any notification.
Article 7
The central competent authority may notify the respective municipal or city/county competent authority to assign personnel to participate in the inspection conducted under these Regulations.
When conducting an inspection, the inspectors shall present the proof of their identity and describe the purpose of the inspection. The inspectors shall have the right to take any actions in order to secure evidences of any violation found under the Act or Medical Devices Good Distribution Practice Regulations.
When conducting an inspection, the inspectors shall present the proof of their identity and describe the purpose of the inspection. The inspectors shall have the right to take any actions in order to secure evidences of any violation found under the Act or Medical Devices Good Distribution Practice Regulations.
Article 8
Upon receipt of the Distribution License, the medical device dealer may fill out a completed application form, with the photocopy of the Distribution License and business permit of the medical device dealer, and pay the application fee for medical devices distribution license certificate (the “Distribution License Certificate”) to the central competent authority
Article 9
As a medical device business permit was cancelled or revoked, its Distribution Licenses, if obtained, will be revoked or withdrawn together by the central competent authority.
For medical device dealers has the Distribution License Certificate, the Certificate shall be returned within fifteen (15) days from the date on which the revocation or withdrawn is imposed; Certificates failed to be returned within the prescribed period shall be cancelled by the central competent authority.
For medical device dealers has the Distribution License Certificate, the Certificate shall be returned within fifteen (15) days from the date on which the revocation or withdrawn is imposed; Certificates failed to be returned within the prescribed period shall be cancelled by the central competent authority.
Article 10
Other than those specified under the preceding article, for medical device dealers whose Distribution License is revoked or withdrawn in accordance of the Act, either in whole or in part, by the central competent authority, its Distribution License Certificate, if obtained, shall be returned within fifteen (15) days from the date on which the revocation or withdrawn is imposed; Certificates failed to be returned within the prescribed period shall be cancelled by the central competent authority.
Article 11
When the medical device dealer is required to hand in its medical device business permit and medical device product licenses pursuant to Paragraph 1, Article 16 of the Act, its Distribution License and Distribution License Certificate shall also be handed in the respective municipal or city/county competent authority for custody, which will be returned upon resumption of the dealer’s business.
When the medical device dealer is required to hand in its medical device business permits and medical device product licenses for cancellation pursuant to Paragraph 3, Article 16 of the Act, its Distribution License and Distribution License Certificate shall also be handed in for cancellation; those failed to be handed in for cancellation shall be cancelled by the central competent authority.
When the medical device dealer is required to hand in its medical device business permits and medical device product licenses for cancellation pursuant to Paragraph 3, Article 16 of the Act, its Distribution License and Distribution License Certificate shall also be handed in for cancellation; those failed to be handed in for cancellation shall be cancelled by the central competent authority.
Article 12
These Regulations shall come into force on the date the Act is implemented.