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{
    "id": 1492390,
    "url": "https://info.mzalendo.com/api/v0.1/hansard/entries/1492390/?format=api",
    "text_counter": 249,
    "type": "speech",
    "speaker_name": "Endebess, UDA",
    "speaker_title": "Hon. (Dr) Robert Pukose",
    "speaker": null,
    "content": " Part (a) of the amendment seeks to enable the country to comply with the World Health Organisation (WHO) standards of manufacturing. This Clause is the most recent WHO organisation prescribed guidelines on good manufacturing practice. Part (b) of the amendment, which is insertion of a new sub-clause immediately after sub-clause 2, seeks to allow the authority to consult and receive advice from the Kenya Nuclear Regulatory Authority that exercises regulatory control over nuclear and radioactive materials and facilities under Section 6(c)(1) of the Nuclear Regulatory Act, No.29 of 2019. This is to require importers, distributors or dealers to keep records of medical devices submitted to the authority."
}