I. | Registration, testing and development of proprietary Chinese medicines ("pCms") and introduction of Good Manufacturing Practice requirements to pCms(10:45 am – 1:10 pm) Meeting with deputations and the Administration
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LC Paper No. CB(2)322/14-15(01)
(issued vide LC Paper No. CB(2)331/14-15 on 24 November 2014) | - | Administration's paper on "Registration and testing of proprietary Chinese medicines"
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LC Paper No. CB(2)322/14-15(02)
(issued on 21 November 2014) | - | Background brief on "Development of Chinese Medicine" prepared by the Legislative Council ("LegCo") Secretariat
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LC Paper No. CB(2)322/14-15(03)
(issued vide LC Paper No. CB(2)331/14-15 on 24 November 2014) | - | Administration's paper on "Introduction of GMP requirement in respect of proprietary Chinese medicines"
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LC Paper No. CB(2)322/14-15(04)
(issued on 21 November 2014) | - | Background brief on "Introduction of GMP requirement in respect of proprietary Chinese medicines" prepared by the LegCo Secretariat
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LC Paper No. CB(2)453/14-15(02)
(issued vide LC Paper No. CB(2)466/14-15 on 15 December 2014) | - | Administration's responses on issues raised at the meeting held on 25 November 2014
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(A list of relevant papers previously issued is available on the Legislative Council website at http://www.legco.gov.hk/yr15-16/english/panels/hs/hs_dcm/papers/dcm_ppr.htm)
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II. | Any other business(1:10 pm – 1:15 pm) Item(s) for discussion at the next meeting |