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{
    "id": 1336292,
    "url": "https://info.mzalendo.com/api/v0.1/hansard/entries/1336292/?format=api",
    "text_counter": 449,
    "type": "speech",
    "speaker_name": "Endebess, UDA",
    "speaker_title": "Hon. (Dr) Robert Pukose",
    "speaker": null,
    "content": " Hon. Temporary Chairlady, I beg to move: THAT, Clause 12 of the Bill be amended by— (a) inserting the following paragraphs immediately after paragraph (e)— ―(ea) regulate the disposal of health products and technologies; (eb) monitor the market for the presence of unregistered and illegal health products and technologies; (ec) conduct analytical tests of health products and technologies; (b) deleting paragraph (f) and substituting therefor the following new paragraph (f) — (f) ensure continuous monitoring of the safety of health products and technologies regulated under this Act through analysis of reports on adverse reactions and events, including any other health product and technology use related issues and take appropriate regulatory actions when necessary‖; (c) deleting paragraph (g) and substituting therefor the following new paragraph (g)— (g) regulate clinical trials and ensure that clinical trial protocols of health products and technologies are being assessed according to the prescribed ethical and professional criteria and defined standards including mandatory bioequivalence studies‖;"
}