Mondaq All Regions - China: Food, Drugs, Healthcare, Life Sciences
Ropes & Gray LLP
In response to the central government's calling for a data protection mechanism,1 the China Drug Administration (the "CDA") ...
Ropes & Gray LLP
On March 17, China's highest legislative body, the National People's Congress, approved a sweeping government restructuring plan.
Ropes & Gray LLP
China's Government will launch several incentives to enhance accessibility of innovative drugs, especially imported oncology drugs.
Ropes & Gray LLP
On March 17, China's highest legislative body, the National People's Congress, approved a sweeping government restructuring plan.
Ropes & Gray LLP
On January 10, 2018, the China Food and Drug Administration announced the implementation of the Technical Guidelines Governing Acceptance of Medical Device Clinical Data from Foreign Studies.
CMS Cameron McKenna Nabarro Olswang LLP
The draft is open for public comments until 25 November 2017.
CMS Cameron McKenna Nabarro Olswang LLP
On 8 October 2017, the General Office of the State Council issued the Opinions on Deepening the Reform of the Evaluation and Approval System and Encouraging the Innovation of Drugs and Medical Devices.
CMS Cameron McKenna Nabarro Olswang LLP
Circular (2014) No.15 provides for the specific deadlines for different domestic medical devices manufacturing companies to gradually meet the Medical Devices Manufacturing Quality Management Standards
HFG Law & Intellectual Property
O Parbleu! Thunderclap for the cheese gourmet! Recently China undertakes strengthened regulatory measures which have directly affected the long-term importation of certain types of European cheese...
CMS Cameron McKenna Nabarro Olswang LLP
The China Food and Drug Administration ("CFDA") promulgated a new circular (2017) No.68 related to the promotion of a drug market authorization holder regime ("MAH Regime") work on 21 August 2017...
Jincheng Tongda & Neal
China has been endeavoring to make comprehensive and fundamental regulatory reform of drug and medical device, in particular in the drug and medical device registration system.
Ropes & Gray LLP
The CFDA is soliciting public comments for these drafts until mid-January 2018.
MyLink Law Office
On 6 June 2016, China Food and Drug Administration ("CFDA") published Administrative Measures on Product Formula Registration of Infant Formula Milk Powder ("Measures") for purpose...
A&Z Law Firm
On September 24th, Ding Jianhua, director of the China Food and Drug Administration (CFDA) Supervision Department, stated at the 2017 Chinese Pharmaceutical Entrepreneurs, Scientists...
CMS Cameron McKenna Nabarro Olswang LLP
After receiving comments on the draft of the Decision of the State Administration of Food and Drug Administration on Adjusting the Relevant Issues Concerning the Registration and Administration...
A&Z Law Firm
Lately many restaurants in Shanghai have been broadcasting the work environment in the kitchen at their entrance (in real-time). What is that about?
Zhong Lun Law Firm
On October 23, 2017, the China Food and Drug Administration ("CFDA") released the revised Administrative Measures for Drug Registration ("Draft for Comment") for public comment.
CMS Cameron McKenna Nabarro Olswang LLP
After the State Council issued the Opinions on Deepening the Reform of Examination and Approval System and Encouraging Innovation of Drugs and Medical Devices ("Opinions") on 8 October 2017, ...
Ropes & Gray LLP
The opinions will create a level playground for R&D-focused drug and device companies, at home and abroad.
Ropes & Gray LLP
The China Food and Drug Administration (CFDA) has published its proposed amendment of the Medical Device Regulations (MDR), previously known as the State Council Order # 650, for public comments.
Most Popular Recent Articles
Ropes & Gray LLP
On March 17, China's highest legislative body, the National People's Congress, approved a sweeping government restructuring plan.
Jincheng Tongda & Neal
China has been endeavoring to make comprehensive and fundamental regulatory reform of drug and medical device, in particular in the drug and medical device registration system.
Ropes & Gray LLP
In response to the central government's calling for a data protection mechanism,1 the China Drug Administration (the "CDA") ...
McDermott Will & Emery
The purchasing power of the Chinese middle class is reshaping the world's market for luxury brands, tourism, real estate, and private investments.
A&Z Law Firm
On September 24th, Ding Jianhua, director of the China Food and Drug Administration (CFDA) Supervision Department, stated at the 2017 Chinese Pharmaceutical Entrepreneurs, Scientists...
Jun He Law Office
Last year ushered in an abundance of new laws and regulations for the pharmaceutical industry in China. Various pharmaceutical policies, including national laws and regulations as well as local supporting policies such as the dual-invoice system, . . .
Ropes & Gray LLP
China's Government will launch several incentives to enhance accessibility of innovative drugs, especially imported oncology drugs.
MyLink Law Office
On 6 June 2016, China Food and Drug Administration ("CFDA") published Administrative Measures on Product Formula Registration of Infant Formula Milk Powder ("Measures") for purpose...
CMS Cameron McKenna Nabarro Olswang LLP
Circular (2014) No.15 provides for the specific deadlines for different domestic medical devices manufacturing companies to gradually meet the Medical Devices Manufacturing Quality Management Standards
Han Kun Law Offices
With the continuous development of cloud computing and internet of things technology, the internet is further reshaping the healthcare industry.
Ropes & Gray LLP
On March 17, China's highest legislative body, the National People's Congress, approved a sweeping government restructuring plan.
Ropes & Gray LLP
On January 10, 2018, the China Food and Drug Administration announced the implementation of the Technical Guidelines Governing Acceptance of Medical Device Clinical Data from Foreign Studies.
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