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Application for registration of proprietary Chinese medicines ends on June 30


The following is issued on behalf of the Chinese Medicine Council of Hong Kong:

The Chinese Medicine Council of Hong Kong (CMCHK) today (June 25) reminded manufacturers or wholesalers of propriety Chinese medicines to submit their applications for the transitional registration of propriety Chinese medicines. The deadline for registration ends on next Wednesday (June 30).

Under the registration system for proprietary Chinese medicines, all proprietary Chinese medicines manufactured, imported, or being possessed in Hong Kong should apply for registration with the CMCHK's Chinese Medicines Board (CMB).

"The registration system for proprietary Chinese medicines is an important milestone in the regulation of Chinese medicines. Through the registration system, the safety, quality and efficacy of proprietary Chinese medicines can be assured, and the health of the citizens can be protected," a CMCHK spokesman said.

Under the registration system, proprietary Chinese medicines which were manufactured or sold in Hong Kong on March 1, 1999 will get transitional registration, provided that the concerned manufacturers or wholesalers of proprietary Chinese medicines submit an application during the application period for transitional registration from December 19, 2003 to June 30, 2004. Late applications will not be accepted.

Proprietary Chinese medicines not eligible for transitional registration should also submit application during the same application period, to allow the CMB to process the applications and issue the certificates of registration as soon as possible.

When the first round of registration work is completed, nobody shall sell, import or possess any unregistered proprietary Chinese medicines in Hong Kong. All registered proprietary Chinese medicines are required to print their registration number on the outer-most package for identification by the public.

In determining an application for registration, the CMB shall take into account the factors of safety, quality and efficacy in respect of the product. The registration requirements include compliance with the standard on limits of heavy metals and toxic elements, pesticides remains and microbes. Besides, the product should not be adulterated with western medicines and it should comply with the law on protection of endangered species.

The details are described in the "Registration of Proprietary Chinese Medicines Application Handbook" for reference by the applicants. The CMB has also developed the "Guidelines for Recall of Chinese Medicine Products", the technical guidelines on testing of proprietary Chinese medicines, and 'Good Clinical Practice for Proprietary Chinese Medicines", to provide guidance for the Chinese medicines traders and pertinent organizations on relevant matters.

The Department of Health shall sample-check the proprietary Chinese medicines sold on the market on a regular basis. When a registered proprietary Chinese medicine is found to be hazardous to health, the CMB will de-register the medicine, and the trader concerned has to recall it from the market.

The "Registration of Proprietary Chinese Medicines Application Handbook" and the application forms are available at Chinese Medicine Division of Department of Health at 32/F, Wu Chung House, 213 Queen's Road East and Chinese Medicines Section at 2/F Public Health Laboratory Centre, 382 Nam Cheong Street, Kowloon. For more details, please telephone 2574 9999 or visit the website of the CMCHK (

Ends/Friday, June 25, 2004


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