Shanghai Qiaosheng Chemical Co., Ltd. Tsamaiso ea Lijo le Lithethefatsi e na le boikarabello ba ho sireletsa bophelo ba sechaba ka ho netefatsa polokeho, ts'ebetso le ts'ireletso ea lithethefatsi tsa batho le tsa bongaka ba liphoofolo, lihlahisoa tsa baeloji le lisebelisoa tsa bongaka; le ka ho netefatsa polokeho ea phepelo ea lijo, litlolo, le lihlahisoa tsa naha ea rona tse ntšang mahlaseli. Ofisiri ea bona website ke FDA.com.
Lenane la libuka tsa basebelisi le litaelo tsa lihlahisoa tsa FDA li ka fumanoa ka tlase. Lihlahisoa tsa FDA li na le tokelo ea molao 'me li tšoailoe ka tlas'a brand Shanghai Qiaosheng Chemical Co., Ltd.
Ithute mokhoa oa ho fana ka katleho files le lifoldara tse sebelisang FDA Electronic Submission Gateway (ESG) NextGen API Guide. Fumana litaelo tse qaqileng mabapi le litlatsetso tsa API, lintho tse hlokahalang pele, le likarolo tsa mosebelisi bakeng sa kopanyo e se nang moeli. Ingolise bakeng sa akhaonto ea Unified Submission Portal (USP) ho fihlella sistimi ea ESG NextGen le ho iketsetsa lits'ebetso tsa hau tsa tlhahiso habonolo. Etsa bonnete ba ho latela melao ka ho sebelisa liakhaonto tsa lengolo-tsoibila tsa khoebo bakeng sa ho ingolisa le ho latela litataiso tsa mohato ka mohato ho qala ka tlhahiso ea API.
Ithute ho sebelisa AS2 Electronic Submission Gateway Next Gen ka tataiso e felletseng ea indasteri. Latela litaelo tsa mohato ka mohato ho fana ka tlhaiso-leseling ea taolo ho FDA ntle le tšitiso. Ntlafatsa tlhophiso ea AS2, ngola litlatsetso, 'me u fumane liteboho ka katleho. Tseba Ts'ebetso ea ho Romela ea AS2 ka Electronic Submission Gateway NextGen AS2 Tataiso ea Basebelisi ba Indasteri Version 2.0 March 2025.
Tlhaloso ea Meta: Hlahloba Mokhoa oa Tlatsetso oa V-8.F bakeng sa Whole Bay Leaves ho tsoa ho Macroanalytical Procedures Manual (MPM) V-8. Ithute mokhoa oa ho sekaseka makhasi a bay bakeng sa litšila tse joalo ka arthropods le hlobo ka mekhoa e felletseng ea tlhahlobo le litataiso tsa tlaleho.
Tlhaloso ea Meta:Fumana kamoo Setsi sa Tsamaiso ea Lijo le Lithethefatsi sa US se laolang Lisebelisoa tsa Bongaka tsa Generative AI-Enabled joalo ka dhac-112024. Ithute ka tumello ea FDA, litaelo tsa tšebeliso, tlhokomelo, le tse ling bukeng ena e rutang ea mosebedisi.
Ithute ka ho kenngwa tshebetsong ha lenaneo la NDA 215014-S-008 Empaveli REMS, tshebetso ya ho fana ka setifikeiti, boitsebiso ba tshebediso, le mehato ya ho obamelwa. Fumana hore na bafani ba tlhokomelo ea bophelo ba ka netefatsoa joang morerong ona oa tlhahlobo oa REMS o ntlafalitsoeng.
Basebelisi ba LearnED LMS ba ka ntlafatsa ts'ireletso ka Multi-factor Authentication (MFA) ba sebelisa smartphone le app ea virtual authenticator. Latela litaelo ho theha sesebelisoa sa hau sa MFA le ho hlahisa likhoutu tsa nako e le 'ngoe bakeng sa ho kena. Lekola tšebelisano le litlhaloso bakeng sa ts'ebetso ea netefatso e se nang moeli.
Fumana lintlha le litaelo tsa tšebeliso ea Super Retinol Cream bakeng sa Banna. Ithute ka motsoako o sebetsang oa Niacinamide, likhetho tsa ho paka, litemoso, le likhothaletso tsa polokelo. Fumana likarabo tsa lipotso tse mabapi le tšebeliso ea sehlahisoa le polokelo.
Fumana buka ea mosebelisi ea Mens Plain Face Cream e nang le litlhaloso tsa sehlahisoa, litaelo tsa tšebeliso, le lipotso tse FAQ. Setlolo sena sa sefahleho se amohetsoeng ke FDA se na le Salicylic acid 2% mme se na le likhetho tse fapaneng tsa ho paka. Ithute ho sebelisa tranelate ena ka katleho le mehato ea bohlokoa eo u lokelang ho e ela hloko. Ikopanye le mofani oa tlhokomelo ea bophelo bakeng sa maemo a itseng a bophelo bo botle kapa mathata.
Tlhaloso ea Meta: Fumana bukana e qaqileng ea mosebelisi ea Anti Aging Cream, e nang le litlhaloso tsa sehlahisoa, litaelo tsa tšebeliso, Lipotso, le tse ling. Ithute ka motsoako oa eona o sebetsang, likhetho tsa ho paka, le mokhoa oa ho o kenyelletsa ts'ebetsong ea hau ea tlhokomelo ea letlalo bakeng sa liphetho tse nepahetseng.
Fumana buka ea mosebelisi bakeng sa Meta Quest 3 Mixed Reality Headset 128 GB, e fanang ka lintlha tse qaqileng, litaelo tsa ho seta, le Lipotso tsa lipotso bakeng sa boiphihlelo bo nepahetseng ba VR. Ithute ka litlhoko tsa hardware, ho seta software, le malebela a ho ntlafatsa boiphihlelo ba hau ba LilypadTM VR.
Tataiso e felletseng ea ho ingolisa, ho kenya tšebetsong, le ho tsamaisa ak'haonte ea hau ho CDER NextGen Portal, ho kenyeletsoa netefatso ea lintlha tse ngata le mekhoa ea ho lokisa password.
Tokomane ena e qaqisa litebello tsa tlhahlobo tsa FDA bakeng sa MedisourceRx, setsi sa ho fana ka litšebeletso kantle ho naha, se entsoeng ho tloha ka la 12-27 Loetse, 2018. E hlalosa mefokolo ea taolo ea boleng, koetliso ea basebetsi, tlhoekiso ea lits'ebeletso, litokomane le lits'ebetso tsa netefatso.
Tataiso ea semmuso bakeng sa basebelisi ba indasteri mabapi le ho fana ka data ka AS2 ho sistimi ea FDA's Electronic Submission Gateway (ESG) NextGen. E kenyelletsa tlhophiso, mokhoa oa ho fana, le ho rarolla mathata.
Litlhaloso tse felletseng le tlhaiso-leseling ea ho odara bakeng sa Pauluhn Meridian FDA luminaire fluorescent, e etselitsoeng lisebelisoa tsa siling tsa mapolanka tse sa feleng tse 300 libakeng tsa leoatle. Likarolo li kenyelletsa multi-voltage elektroniki ballast, tse fapa-fapaneng lamp dikgetho, le disetifikeiti joaloka IP52 le UL1598A.
Tseba ka Murrplastik's KDL/H-VA-FDA le KDP FDA Cablequick Series ea litsamaiso tsa ho kenya likhoele. Liforeimi tsena tsa tšepe tse sa hloekang tse nang le li-grommets tsa TPE tse lumellanang le FDA li fana ka lithapo tse phahameng tsa motlakase, ho kenya habonolo, le ts'ireletso ea tikoloho bakeng sa indasteri ea lijo le meriana. Ho fanoe ka lintlha tse mabapi le boholo ba foreimi, ho tsamaellana le bophara ba cable, le likarolo tsa linomoro.
Bukana ea semolao e hlalosang maano le mekhoa ea Setsi sa Tlhahlobo le Lipatlisiso tsa Lithethefatsi (CDER) Interdisciplinary Review Sehlopha (IRT) mabapi le lithuto tsa Thorough QT (TQT), ho kenyeletsoa tataiso mabapi le tlhahlobo ea lefu la pelo bakeng sa nts'etsopele ea lithethefatsi.
Qala ka k'hamera ea hau ea Sony Alpha 1 (ILCE-1M2) e se nang seipone. Tataiso ena e akaretsa ho seta, lisebelisoa, ho tjhaja, sehokelo sa lense, tlhophiso ea mantlha, le litaelo tsa mantlha tsa ho thunya.
Tokomane ena e hlahisa FDA's Compliance Programme for Postmarketing Adverse Drug Experience (PADE) Reporting Inspections, e qaqisa mekhoa, litlhoko, le boikarabello ba ho netefatsa boits'oaro ba tšireletso ea lithethefatsi.
Tataiso e felletseng ho tsoa ho Tsamaiso ea Lijo le Lithethefatsi ea US (FDA) e hlalosang litekanyetso tsa taolo ea boleng, mekhoa ea tlhahlobo, le ho latela melaoana bakeng sa letsatsi.amp lihlahisoa le ultraviolet lamps. E hatisitsoe ka March 1988.
FDA Foromo ea 483 e hlalosang maikutlo a tlhahlobo ho Central Admixture Pharmacy Services Inc., moetsi oa lihlahisoa tsa lithethefatsi tse sa hloekang, tse koahelang tlhokomelo ea lisebelisoa, netefatso ea ho thibela likokoana-hloko, mekhoa ea tokollo ea sehlahisoa, liaparo tsa basebetsi le bohloeki ba ts'ebetso ea aseptic.
Lekola karolo e felletseng ea Tsamaiso ea Lijo le Lithethefatsi ea US (FDA) ho laola li-cannabis le lihlahisoa tse nkiloeng ho cannabis. Tokomane ena e qaqisa lithahasello tsa leano la FDA, melao ea molao tlasa FDCA le CSA, phello ea Bili ea Temo, lits'ebetso tsa nts'etsopele ea lithethefatsi, le melaoana e ikhethileng ea lihlahisoa tsa lijo, li-supplement le litlolo.
Ho fedileview ea Pharmaceutical Quality System (PQS) e hlahisitsoeng ke FDA, e shebane le CGMPs, ICH Q10, le maano a tlhahlobo ea FDA. Ithute ka litebello tsa boleng le litlhokahalo tsa taolo bakeng sa tlhahiso ea meriana.
