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FDA muPhilippine inotarisira kudzora e-fodya: zvigadzirwa zvehutano kwete zvigadzirwa zvevatengi

Musi waChikunguru 24, maererano nemishumo yekune dzimwe nyika, iyo Philippine FDA yakati kutariswa kwefodya yefodya, e-fodya uye zvimwe zvinopisa fodya zvigadzirwa (HTP) inofanira kunge iri basa rekudya neDrug Administration (FDA) uye haifanirwe kuve. kuendeswa kuPhilippine Dhipatimendi rekutengeserana neindasitiri (DTI), nekuti zvigadzirwa izvi zvinosanganisira hutano hweveruzhinji.

FDA yakajekesa chinzvimbo chayo mukutaura kwayo mukutsigira Ministry of Health (DOH) ichikumbira mutungamiri wenyika kuti asaite mutemo wefodya yemagetsi (Senate bill 2239 uye House bill 9007), iyo yakaendesa hwaro hwehutongi hwekutonga.

"DOH inoita mvumo yebumbiro kuburikidza neFDA, uye inochengetedza kodzero yehutano hwemunhu wese wemuPhilippines nekutanga hurongwa hwekutonga hunoshanda."Chirevo cheFDA chakadaro.

Kusiyana nematanho akarongwa, FDA yakati zvigadzirwa zvefodya zvemagetsi neHTP zvinofanirwa kutorwa sezvigadzirwa zvehutano, kwete zvinhu zvevatengi.

“Izvi zvinodaro nekuti indasitiri iri kushambadzira zvinhu zvakaita semidzanga yefodya yechinyakare, uye vamwe vanhu vanototaura kana kutaura kuti zvigadzirwa izvi hazvina njodzi kana kukuvadza zvishoma.FDA yakati.