News

1. Kushomeka kwemanucleic acid ekuona kits kuchava dambudziko repasi rose.

2. Chinese IVD mabhizinesi ane kugona kuenda kunze kwenyika uye kukwikwidza nenyika-mabhizinesi ekirasi.

3, yemusika yekuyedza reagent chaos, iyo drug regulatory official action!

Mazhinji mabhizinesi eIVD akawana yekutanga batch yezvitupa zvekunze kune zvigadzirwa zvavo zvitsva zve corona

Kusvika pari zvino, State Administration yeChikafu neDrug Administration yakabvumidza makumi maviri kubuda - e -
Sekureva kweThe West China Securities Research Report, nyika inodya zviuru mazana mashanu kusvika mazana manomwe emakumi manomwe ezviuru zvekuongorora makitsi zuva rega rega. Kushomeka kwema nucleic acid ekuyedza kits richava dambudziko repasi rose, ukuwo kudiwa kwepamusoro - hunyanzvi hwekiti hwakagadzirwa muChina hunotarisirwa kuramba hwakakwira.

Tsvagiridzo yeshumo data inoratidza kuti nyika dzinosvika makumi maviri nenhanhatu dzakaendesa maodha ekupa kuChina, nemakiti anodarika mamirioni gumi nemashanu akarairwa. "Kushomeka kwakanyanya kwemanovel Coronavirus yekuona kits uye ZVINHU zvekudzivirira zvinoramba zvisina kugadziriswa," iyo AMA yakadaro mukutaura neChipiri.

Munguva pfupi yapfuura, akati wandei eIVD bhizinesi nyowani zvigadzirwa zvekorona nekutanga certification yekunze pamusika. Pakati pemakambani akanyorwa, makambani mapfumbamwe akanyorwa, anosanganisira Meikang Biotechnology, Peoson Biotechnology, Cape Biotechnology, Anke Biotechnology, Daan Genomics, Wanfu Biotechnology, Mike Biotechnology neHangzhou Realytech, vanoti zvigadzirwa zvavo zvakawana THE EU CE certification.

AusDiagnostics inc., Roche Diagnostics Inc., Vivacheck Inc., Zhijiang Group LTD., CTK Group LTD. (TGA) uye Hollogier Group Inc. (TGA) musi weMugovera, March 22, maererano neAustralian Drug Administration (TGA). Hangzhou Otai, Vivacheck uye Shanghai Zhijiang mabhizinesi epamba IVD.

MuUnited States, maererano newebhusaiti yepamutemo yeFDA, chaiyo-nguva fluorescent RT-PCR kit inogadzirwa neBGI yekuonekwa kweSARS-2019-NCOV yakabvumidzwa neFDA uye inogona kuiswa zviri pamutemo mukudzivirira nekudzora denda muUnited States. Ichi ndicho chekutanga chigadzirwa cheChinese chakapfuura mvumo yeFDA yekukurumidzira.
Muchokwadi, maChinese IVD mabhizinesi ane kugona kuenda kunze kwenyika uye kukwikwidza nenyika - ekirasi mabhizinesi.

Hangzhou Realytech yakapfuura IYO FDA certification. Iyo novel Coronavirus yekuona mwero wakakwira. Ndapota inzwa wakasununguka kutibata nesu kana uchidatenga coronavirus inokurumidza kuona reagent yakawanda.


Nguva yekutumira: Jul-15-2020