Thông tư số 05/2010/TT-BYT do Bộ Y tế ban hành ngày 01 tháng 03 năm 2010 hướng dẫn chi tiết về việc bảo mật dữ liệu thử nghiệm lâm sàng và dữ liệu bí mật thương mại trong quá trình đăng ký lưu hành thuốc tại Việt Nam. Dưới đây là nội dung phân tích chi tiết các điều khoản đầu tiên (từ Điều 1 đến Điều 4) của Thông tư này:
- Phạm vi điều chỉnh (Điều 1)
Điều 1 quy định rõ phạm vi áp dụng của Thông tư, tập trung vào các nội dung cốt lõi sau:
- Hướng dẫn trình tự, thủ tục và các yêu cầu kỹ thuật đối với việc bảo mật dữ liệu thử nghiệm lâm sàng, dữ liệu tiền lâm sàng và các dữ liệu bí mật thương mại khác được nộp trong hồ sơ đăng ký thuốc.
- Áp dụng đối với các hồ sơ đăng ký thuốc mới, bao gồm cả thuốc hóa dược mới, sinh phẩm y tế mới nhằm bảo vệ quyền lợi hợp pháp của người nộp đơn trước các hành vi sử dụng thương mại không lành mạnh.
- Đối tượng áp dụng (Điều 2)
Thông tư xác định rõ các nhóm đối tượng chịu sự điều chỉnh trực tiếp bao gồm:
- Các tổ chức, cá nhân trong nước và nước ngoài thực hiện hoạt động đăng ký thuốc lưu hành tại Việt Nam.
- Các cơ quan quản lý nhà nước về dược, cụ thể là Cục Quản lý Dược thuộc Bộ Y tế và các đơn vị, cá nhân được giao nhiệm vụ tiếp nhận, thẩm định, quản lý hồ sơ đăng ký thuốc.
- Giải thích từ ngữ (Điều 3)
Để đảm bảo tính thống nhất trong việc áp dụng pháp luật, Điều 3 đưa ra định nghĩa cho các thuật ngữ chuyên ngành quan trọng:
- Dữ liệu thử nghiệm: Là toàn bộ các kết quả thử nghiệm lâm sàng, thử nghiệm tiền lâm sàng (bao gồm thử nghiệm dược lý, độc tính) và các dữ liệu kỹ thuật khác chứng minh tính an toàn, hiệu quả của thuốc.
- Thuốc mới: Là thuốc chứa dược chất mới, phối hợp mới của các dược chất đã lưu hành hoặc thuốc có chỉ định mới, đường dùng mới, dạng bào chế mới chưa từng được cấp phép lưu hành tại Việt Nam.
- Sử dụng thương mại không lành mạnh: Hành vi sử dụng dữ liệu thử nghiệm của người nộp đơn trước đó để cấp phép cho một sản phẩm khác mà không được sự đồng ý của người sở hữu dữ liệu, hoặc tiết lộ dữ liệu đó cho bên thứ ba vì mục đích thương mại.
- Nguyên tắc bảo mật dữ liệu thử nghiệm (Điều 4)
Đây là điều khoản nền tảng thiết lập cơ chế bảo hộ dữ liệu, bao gồm các nguyên tắc nghiêm ngặt sau:
- Trách nhiệm của cơ quan quản lý: Cục Quản lý Dược có trách nhiệm bảo mật các dữ liệu thử nghiệm có trong hồ sơ đăng ký thuốc, không được tiết lộ cho bất kỳ bên thứ ba nào, trừ trường hợp cần thiết để bảo vệ công chúng hoặc khi đã có biện pháp bảo đảm dữ liệu không bị sử dụng thương mại không lành mạnh.
- Thời hạn bảo hộ dữ liệu: Cơ quan quản lý không được sử dụng dữ liệu thử nghiệm của người nộp đơn trước để thẩm định và cấp số đăng ký cho người nộp đơn sau đối với thuốc tương tự, trừ khi có sự đồng ý của người nộp đơn trước hoặc thời hạn bảo hộ dữ liệu đã hết (thông thường là 05 năm kể từ ngày thuốc của người nộp đơn trước được cấp phép lưu hành).
- Yêu cầu đối với người nộp đơn: Người nộp đơn muốn được bảo mật dữ liệu phải có văn bản yêu cầu bảo mật kèm theo hồ sơ đăng ký thuốc, trong đó chỉ rõ các tài liệu, dữ liệu cần được bảo mật theo quy định.
Để sử dụng toàn bộ tiện ích nâng cao của Hệ Thống Pháp Luật vui lòng lựa chọn và đăng ký gói cước.
| THE MINISTRY OF HEALTH | SOCIALIST REPUBLIC OF VIET NAM |
| No. 05/2010/TT-BYT | Hanoi, March 01, 2010 |
CIRCULAR
GUIDING THE KEEPING OF CONFIDENTIALITY OF TRIAL DATA IN MEDICINE REGISTRATION
THE MINISTRY OF HEALTH
Pursuant to June 14, 2005 Law No. 34/2005/ QH11 on Pharmacy;
Pursuant to November 29, 2005 Law No. 50/2005/QH11 on Intellectual Property, which was amended and supplemented by June 19, 2009 Law No. 36/2009/QH12 Amending and Supplementing a Number of Articles of the Law on Intellectual Property;
Pursuant to the Government's Decree No. 188/2007/ND-CP of December 27, 2007, defining the functions, tasks, powers and organizational structure of the Ministry of Health;
Pursuant to the Government's Decree No. 103/2006/ND-CP of September 22, 2006, detailing and guiding the implementation of a number of articles of the Law on Intellectual Property on industrial property;
The Ministry of Health guides the keeping of confidentiality of trial data in medicine registration as follows:
Chapter I
GENERAL PROVISIONS
Article 1. Scope of regulation
1. This Circular guides the request and procedures for keeping confidentiality of trial data in medicine registration.
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Article 2. Subjects of application
This Circular is applicable to Vietnamese and foreign organizations and individuals that conduct medicine registration related activities in Vietnam.
Article 3. Interpretation of terms
In this Circular, the following terms and expressions are construed as follows:
1. Medicine means a substance or mixture of substances for human use for disease prevention, treatment or diagnosis or adjustment of physiological functions of human body, including finished medicine products, medicine materials, vaccines and medical biologicals other than functional foods.
2. Active ingredient (also pharmaceutical active ingredient or pharmakon) means a substance or mixture of substance of substances having a therapeutic activity and used in medicine manufacture.
3. New active ingredient means an active ingredient which has never been permitted for circulation in Vietnam and not yet permitted for circulation in anywhere else in the world for 12 months counting back from the date of filing the application for registration of a medicine containing such ingredient in Vietnam.
4. Keeping confidentiality of data and trial data (below collectively referred to as keeping data confidentiality) means keeping confidentiality of pharmaceutical trial data in the process of medicine registration specified in Article 128 of the Law on Intellectual Property and Article 20 of the Government's Decree No. 103/2006/ND-CP of September 22, 2006, detailing and guiding the implementation of a number of articles of the Law on Intellectual Property on industrial property.
5. Circular on medicine registration means the Minister of Health's Circular No. 22/2009/ TT-BYT of November 24, 2009, on medicine registration.
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The Vietnam Drug Administration is the agency responsible for keeping data confidentiality in medicine registration under this Circular.
Chapter II
CONDITIONS ON KEEPING DATA CONFIDENTIALITY
Article 5. Data to be kept confidential
Data to be kept confidential include data of clinical trials of medicines containing new active ingredients provided by medicine-registering establishments in medicine registration dossiers (for use in proving the safety and desired effects of medicines under the Circular on medicine registration) and satisfying the conditions specified in Article 6 of this Circular.
Article 6. Conditions for data to be kept confidential
Data will be kept confidential when fully satisfying the following conditions:
1. They constitute a business secret which satisfies the protection conditions specified in Clause 23. Article 4, and Article 84 of the Law on Intellectual Property.
2. They are an outcome of a substantial investment of labor;
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Chapter III
CONDITIONS FOR AND ORDER OF RECEIVING MEDICINE REGISTRATION DOSSIERS SUBJECT TO DATA CONFIDENTIALITY KEEPING REQUESTS
Article 7. Conditions for receiving medicine registration dossiers subject to data confidentiality keeping requests
1. Apart from satisfying the general requirements on dossiers specified in the Circular on medicine registration, a medicine registration dossier subject to a data confidentiality keeping request must also contain at least the following documents:
a/ An application for medicine registration, made according to a set form provided in the Circular on medicine registration (not printed herein), in which the medicine-registering establishment shall express its data confidentiality keeping request by ticking in an appropriate box for such request and enumerate documents showing data requested to be kept confidential;
b/ Documents showing data requested to be kept confidential, which must be presented as clinical reports as prescribed in the Circular on medicine registration.
2. All the above documents must be appended with a "confidential" stamp, enveloped in a separate package, which is sealed and appended with a "confidential" stamp.
Article 8. Order of receiving medicine registration dossiers subject to data confidentiality keeping requests
A medicine registration dossier subject to a data confidentiality keeping request shall be received by the Vietnam Drug Administration in the following order:
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2. Checking the appearance of the confidential document package before breaking the seal and checking the format of documents contained therein under Point b. Clause 1, Article 7 of this Circular.
3. Comparing documents contained in the confidential document package against documents listed in the data confidentiality keeping request.
4. Recording the data confidentiality keeping request in the register of received dossiers and dossier receipts, and at the same time re-sealing the confidential document package, for dossiers satisfying the conditions specified in Article 7 of this Circular. If medicine registration dossiers subject to data confidentiality keeping requests fail to satisfy the conditions specified in Article 7 of this Circular, the Vietnam Drug Administration shall receive only medicine registration dossiers of registering establishments that withdraw their data confidentiality keeping requests.
Chapter IV
KEEPING OF DATA CONFIDENTIALITY
Article 9. Acceptance of data confidentiality keeping requests
1. For accepted medicine registration dossiers subject to data confidentiality keeping requests (except for those specified in Article 10 of this Circular), the Vietnam Drug Administration shall also accept data confidentiality keeping requests and take confidentiality-keeping measures specified in Article 12 of this Circular.
2. Decisions on acceptance of data confidentiality keeping requests shall be notified by the Vietnam Drug Administration to medicine-registering establishments and published on the Vietnam Drug Administration's website together with notices of decisions on grant of medicine circulation registration numbers.
Article 10. Refusal to keep data confidentiality
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a/ Data requested to be kept confidential are not those specified in Article 5 of this Circular;
b/ Medicine in the medicine registration dossier subject to data confidentiality keeping request is not permitted for circulation in Vietnam:
c/ There is a ground to believe that the data requested to be kept confidential fail to satisfy at least one of the confidentiality keeping conditions specified in Article 6 of this Circular;
d/ Keeping data confidentiality might cause serious impacts on human health.
2. Notices of refusal to keep data confidentiality shall be sent by the Vietnam Drug Administration to medicine-registering establishments together with notices of decisions to grant or on refusal to grant medicine circulation registration numbers, clearly stating the reasons for refusal.
Article 11. Opinions of a third party on keeping data confidentiality
1. From the date a decision on acceptance of a data confidentiality keeping request is announced, all organizations and individuals may request the Vietnam Drug Administration to terminate the keeping of data confidentiality under Article 14 of this Circular.
2. A request for termination of the keeping of data confidentiality must be made in writing, according to a set form provided in this Circular (not printed herein), and enclosed with documents or quotations of information sources to support the request.
3. Within 15 working days after receiving a request for termination of the keeping of data confidentiality, the Vietnam Drug Administration shall notify such in writing to the medicine-registering establishment whose data are kept confidential. Within 3 working months after the Vietnam Drug Administration signs a written notice, the medicine-registering establishment shall send a written reply to explain the reason(s) for keeping, and supply necessary documents and evidence as requested in the notice.
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Article 12. Data confidentiality keeping measures
In case a request for data confidentiality is accepted, the Vietnam Drug Administration shall take the following measures:
1. Archiving and managing documents showing data requested to be kept confidential under regulations on management of secret documents.
2. Preventing any third party from accessing confidential data unless the access to these data by a competent management agency aims to verify results of a clinical trial, safety and effect of a medicine or to meet requirements of public health care.
3. Abstaining from disclosing data, unless the disclosure is necessary to protect the public.
4. Temporarily refusing to consider and grant permits to medicine-registering establishments that file their registration dossiers later than a dossier with confidential data, in case dossiers of establishments with later application dates refer to data currently kept confidential without the consent of the medicine-registering establishment whose data is kept confidential and establishments with later application dates cannot prove that data referred to in their dossiers are created independently from confidential data.
Article 13. Duration of keeping data confidentiality
1. The data confidentiality keeping measures specified in Clauses 1,2 and 3 of Article 12 shall be applied from the date the data are filed to the date the data are disclosed. However, the duration of keeping data confidentiality must not exceed the duration of management of secret documents prescribed in current regulations.
2. The data confidentiality keeping measure specified in Clause 4, Article 12 shall be applied from the date the data are filed to the date of expiration of the 5-year validity of a medicine circulation permit granted to a medicine-registering establishment having confidential data.
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Mọi chi tiết xin liên hệ: ĐT: (028) 3930 3279 DĐ: 0906 22 99 66
The keeping of data confidentiality shall be partially or wholly terminated in the following cases:
1. Data no longer satisfy the confidentiality keeping conditions specified in Article 6 of this Circular.
2. A competent agency has grounds to believe that the medicine-registering establishment having data currently kept confidential has no lawful right to use these data.
3. A decision to grant a circulation permit for a medicine with confidential data is no longer valid or the medicine registration number is revoked or the medicine-registering establishment voluntarily requests revocation of the registration number.
4. A competent agency issues a decision to compel the licensing of a patent on the medicine with confidential data.
5. An agency competent to settle complaints issues a decision to invalidate a decision on acceptance of a data confidentiality keeping request.
6. Termination of the keeping of data confidentiality is needed to protect public health and meet the society's urgent needs.
Chapter V
RIGHTS AND OBLIGATIONS OF ESTABLISHMENTS HAVING CONFIDENTIAL DATA
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A medicine-registering establishment having confidential data has the following rights:
1. To prevent other medicine-registering establishments from using confidential data for unhealthy commercial purposes, including illegal use of data for filing medicine registration applications.
2. To lodge a complaint with the Vietnam Drug Administration on suspicion of a disclosure or illegal use of confidential data for filing a medicine registration application.
Article 16. Obligations of medicine-registering establishments having confidential data
A medicine-registering establishment having confidential data has the following obligations:
1. To prove its holding of the right to the data and that the data fully satisfy the conditions to be kept confidential at the request of the Vietnam Drug Administration in the case specified in Clause 3. Article 11 of this Circular.
2. To evidence the disclosure and/or illegal use of confidential data for unhealthy commercial purposes in case it exercises its rights provided in Article 15 of this Circular.
Chapter VI
ORGANIZATION OF IMPLEMENTATION
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1. This Circular takes effect 45 days from the date of its signing.
2. This Circular replaces the Minister of Health's Decision No. 30/2006/QD-BYT of September 30, 2006, promulgating the Regulation on keeping confidentiality of data in medicine registration dossiers. Dossiers subject to data confidentiality keeping requests filed with the Vietnam Drug Administration before the effective date of this Circular shall be examined and examination results shall be notified under the said Regulation.
3. Any problems arising in the course of implementation should be promptly reported to the Ministry of Health (the Vietnam Drug Administration) for consideration and settlement.-
FOR THE MINISTER OF HEALTH
DEPUTY MINISTER
Cao Minh Quang
- 1Circular No. 22/2009/TT-BYT of November 24, 2009, on registration of drugs
- 2Law No. 36/2009/QH12 of June 19, 2009, amending and supplementing a number of articles of the Law on intellectual property
- 3Decree No. 188/2007/ND-CP of December 27, 2007, defining the functions, tasks, powers and organizational structure of the Ministry of Health.
- 4Decree of Government No. 103/2006/ND-CP of September 22, 2006 detailing and guiding the implementation of a number of articles of The Law on Intellectual Property regarding industrial property
- 5Law No. 50/2005/QH11 of November 29, 2005, on Intellectual property.
- 6Law No. 34/2005/QH11 of June 14, 2005, on pharmacy
Circular No. 05/2010/TT-BYT of March 01, 2010, guiding the keeping of confidentiality of trial data in medicine registration
- Số hiệu: 05/2010/TT-BYT
- Loại văn bản: Thông tư
- Ngày ban hành: 01/03/2010
- Nơi ban hành: Bộ Y tế
- Người ký: Cao Minh Quang
- Ngày công báo: Đang cập nhật
- Số công báo: Đang cập nhật
- Ngày hiệu lực: 15/04/2010
- Tình trạng hiệu lực: Kiểm tra
