{"id":8743,"date":"2025-12-22T01:22:18","date_gmt":"2025-12-22T01:22:18","guid":{"rendered":"https:\/\/pharmamachinecn.com\/?p=8743"},"modified":"2026-02-05T02:48:49","modified_gmt":"2026-02-05T02:48:49","slug":"sop-for-capsule-counting-machine","status":"publish","type":"post","link":"https:\/\/pharmamachinecn.com\/tr\/sop-for-capsule-counting-machine\/","title":{"rendered":"Kaps\u00fcl Sayma Makinesinin Kurulumu, \u00c7al\u0131\u015ft\u0131r\u0131lmas\u0131 ve Kapat\u0131lmas\u0131 i\u00e7in Standart \u0130\u015flem Prosed\u00fcr\u00fc (SOP)."},"content":{"rendered":"
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Kaps\u00fcl say\u0131m prosed\u00fcr\u00fc (SOP) belgesi, bir ila\u00e7 \u00fcretim tesisinde kaps\u00fcl say\u0131m\u0131n\u0131n nas\u0131l yap\u0131lmas\u0131 gerekti\u011fini kontrol eden bir GMP gereklili\u011fidir. Standart bir i\u015fletim prosed\u00fcr\u00fc olmadan, say\u0131m \u00f6znel, tutars\u0131z ve riskli hale gelir.<\/p>

\"Kullan\u0131m
Kaps\u00fcl Sayma Makinesi i\u00e7in Standart \u00c7al\u0131\u015fma Prosed\u00fcr\u00fc (SOP)<\/strong><\/figcaption><\/figure>

A\u015fa\u011f\u0131da, ila\u00e7 end\u00fcstrisinde yayg\u0131n olarak kullan\u0131lan kaps\u00fcl say\u0131m prosed\u00fcrlerini (SOP) payla\u015faca\u011f\u0131z. Bunlar\u0131, tesisinizin s\u00fcre\u00e7lerine g\u00f6re uyarlanm\u0131\u015f kendi \u00f6zel SOP'nizi olu\u015fturmak i\u00e7in referans olarak kullanabilir veya kullan\u0131ma haz\u0131r belgemizi indirebilirsiniz.<\/p>

1.0 Ama\u00e7<\/b><\/strong><\/h2>

Bu tablet\/kaps\u00fcl say\u0131m makinesi prosed\u00fcr\u00fcn\u00fcn amac\u0131, kaps\u00fcl say\u0131m makinesinin haz\u0131rlanmas\u0131, \u00e7al\u0131\u015ft\u0131r\u0131lmas\u0131, do\u011frulanmas\u0131, belgelendirilmesi ve temizlenmesi i\u00e7in ad\u0131m ad\u0131m prosed\u00fcr\u00fc tan\u0131mlamakt\u0131r. Bu prosed\u00fcr, her \u015fi\u015fe, po\u015fet veya kab\u0131n, Parti \u00dcretim Kayd\u0131'na (BMR) g\u00f6re do\u011fru say\u0131da kaps\u00fcl almas\u0131n\u0131 sa\u011flar.<\/p>

Bu standart i\u015fletim prosed\u00fcr\u00fc (SOP), kaps\u00fcl say\u0131m i\u015flemleri s\u0131ras\u0131nda say\u0131m hatalar\u0131n\u0131, kar\u0131\u015f\u0131kl\u0131klar\u0131, \u00e7apraz kontaminasyonu ve sapmalar\u0131 \u00f6nlemeyi de ama\u00e7lamaktad\u0131r.<\/p>

2.0 Kapsam<\/b><\/strong><\/h2>

Bu standart i\u015fletim prosed\u00fcr\u00fc \u015funlar i\u00e7in ge\u00e7erlidir:<\/p>

2.0.1: \u00dcretim veya paketleme alan\u0131nda kaps\u00fcl sayma faaliyetlerine atanm\u0131\u015f t\u00fcm operat\u00f6rler.<\/p>

2.0.2: Kaps\u00fcl say\u0131m i\u015flemlerini denetleyen \u00fcretim sorumlular\u0131.<\/p>

2.0.3: Belgeleri incelemek ve onaylamakla sorumlu Kalite G\u00fcvence (KG) personeli.<\/p>

2.0.4: A\u011f\u0131zdan al\u0131nan kat\u0131 dozaj formlar\u0131 i\u00e7in kullan\u0131lan, yar\u0131 otomatik veya otomatik her t\u00fcrl\u00fc kaps\u00fcl sayma makinesi.<\/p>

3.0 Sorumluluk<\/b><\/strong><\/h2>

3.0.1: Bu madde, standart i\u015fletim prosed\u00fcrlerine (SOP'lere) uyuldu\u011fundan emin olmaktan sorumlu \u00e7al\u0131\u015fanlar\u0131 i\u00e7erir.<\/p>

3.1 Operat\u00f6r<\/b><\/strong><\/h3>

3.1.1: \u00c7al\u0131\u015ft\u0131rmadan \u00f6nce makineyi ve malzemeleri haz\u0131rlay\u0131n.<\/p>

3.1.2: Kaps\u00fcl veya tablet sayma makinesini bu prosed\u00fcre uygun olarak \u00e7al\u0131\u015ft\u0131r\u0131n.<\/p>

3.1.3: Kaps\u00fcl boyutu, miktar\u0131, h\u0131z\u0131 ve parti ayr\u0131nt\u0131lar\u0131 i\u00e7in do\u011fru ayarlar\u0131n yap\u0131ld\u0131\u011f\u0131ndan emin olun.<\/p>

3.1.4: Gerekti\u011finde i\u015flem i\u00e7i kontrolleri, makine ayarlamalar\u0131n\u0131 ve durdurmalar\u0131 ger\u00e7ekle\u015ftirin.<\/p>

3.1.5: T\u00fcm verileri ger\u00e7ek zamanl\u0131 olarak BMR'ye ve ilgili kay\u0131tlara kaydedin.<\/p>

3.1.6: Herhangi bir tutars\u0131zl\u0131k veya anormalli\u011fi derhal \u00dcretim Sorumlusuna bildirin.<\/p>

3.2 \u00dcretim Sorumlusu<\/b><\/strong><\/h3>

3.2.1: \u00c7al\u0131\u015ft\u0131rmadan \u00f6nce makinenin do\u011fru \u015fekilde kuruldu\u011fundan emin olun.<\/p>

3.2.2: Say\u0131m i\u015fleminin onaylanm\u0131\u015f BMR'ye uygun olarak ger\u00e7ekle\u015ftirildi\u011finden emin olun.<\/p>

3.2.3: \u0130\u015flem \u00f6ncesinde ve sonras\u0131nda hat temizli\u011finin sa\u011fland\u0131\u011f\u0131ndan emin olun.<\/p>

3.2.4: Operat\u00f6r taraf\u0131ndan bildirilen tutars\u0131zl\u0131klar\u0131 veya anormallikleri ara\u015ft\u0131r\u0131n.<\/p>

3.2.5: Operat\u00f6rlerin GMP, g\u00fcvenlik ve dok\u00fcmantasyon standartlar\u0131na uymas\u0131n\u0131 sa\u011flay\u0131n.<\/p>

3.3 Kalite G\u00fcvencesi (KG)<\/b><\/strong><\/h3>

3.3.1: Tamamlanm\u0131\u015f BMR giri\u015flerini, devam eden kontrolleri ve kay\u0131tlar\u0131 inceleyin.<\/p>

3.3.2: SOP, GMP ve d\u00fczenleyici gerekliliklere uygunlu\u011fu do\u011frulay\u0131n.<\/p>

3.3.3: Temizlik ve dok\u00fcmantasyon incelemesinin ard\u0131ndan, bir sonraki parti i\u00e7in ekipman\u0131n kullan\u0131ma sunulmadan \u00f6nce onaylanmas\u0131.<\/p>

4.0 Gerekli Ekipman ve Malzemeler<\/b><\/strong><\/h2>

Operat\u00f6rler, faaliyete ba\u015flamadan \u00f6nce a\u015fa\u011f\u0131da listelenen t\u00fcm gerekli malzemelerin mevcut oldu\u011fundan emin olmal\u0131d\u0131r.<\/p>

4.0.1: Do\u011fru kaps\u00fcl boyutuna ula\u015fmak i\u00e7in t\u00fcm par\u00e7alar\u0131 monte edilmi\u015f tablet\/kaps\u00fcl sayma makinesi.<\/p>

4.0.2: BMR'de belirtildi\u011fi gibi bo\u015f \u015fi\u015feler, po\u015fetler veya kaplar.<\/p>

4.0.3: Parti \u00dcretim Kayd\u0131 (BMR).<\/p>

4.0.4: Barkod veya bas\u0131l\u0131 etiketler (varsa).<\/p>

4.0.5: Temizlik ara\u00e7lar\u0131: f\u0131r\u00e7alar, onayl\u0131 temizlik maddeleri ve t\u00fcy b\u0131rakmayan mendiller.<\/p>

4.0.6: Eldivenler ve koruyucu giysiler.<\/p>

4.0.7: Kalibrasyon a\u011f\u0131rl\u0131klar\u0131 (a\u011f\u0131rl\u0131k bazl\u0131 do\u011frulama kullan\u0131l\u0131yorsa).<\/p>

5.0 Prosed\u00fcr<\/b><\/strong><\/h2>

\u0130\u015fte herkesin izlemesi gereken prosed\u00fcr:<\/p>

5.1 Standart \u0130\u015flem Prosed\u00fcr\u00fc Amac\u0131n\u0131n Do\u011frulanmas\u0131<\/b><\/strong><\/h3>

5.1.1: Ba\u015flamadan \u00f6nce BMR'yi ve bu SOP'yi okuyun ve anlay\u0131n.<\/p>

5.1.2: \u00dcr\u00fcn ad\u0131n\u0131, g\u00fcc\u00fcn\u00fc, kaps\u00fcl boyutunu, parti numaras\u0131n\u0131 ve dolum miktar\u0131n\u0131 onaylay\u0131n.<\/p>

5.2 Operasyon \u00d6ncesi Haz\u0131rl\u0131k<\/b><\/strong><\/h3>

5.2.1: Makinenin temiz oldu\u011fundan ve ekipman durum etiketinde \u201cTemizlendi\u201d ibaresinin bulundu\u011fundan emin olun.<\/p>

5.2.2: Kaps\u00fcl sayac\u0131n\u0131 'A\u00c7IK' konuma getirin.<\/p>

5.2.3: Se\u00e7iniz:<\/p>

5.2.3.1: Do\u011fru kaps\u00fcl boyutu<\/p>

5.2.3.2: \u015ei\u015fe ba\u015f\u0131na gerekli miktar<\/p>

5.2.3.3: \u00dcretim h\u0131z\u0131 veya titre\u015fim seviyesi<\/p>

5.2.3.4: Parti detaylar\u0131 (makine giri\u015f gerektiriyorsa)<\/p>

5.2.4: Az say\u0131da tablet veya kaps\u00fclle k\u0131sa bir test yap\u0131n.<\/p>

5.2.5: Hazne ve oluktan ge\u00e7i\u015fin sorunsuz olup olmad\u0131\u011f\u0131n\u0131 kontrol edin.<\/p>

5.2.6: Fotoelektrik veya mekanik sens\u00f6rlerin do\u011fru okuma yapt\u0131\u011f\u0131n\u0131 do\u011frulay\u0131n.<\/p>

5.2.7: Kaps\u00fcller s\u0131k\u0131\u015f\u0131rsa veya t\u0131kan\u0131rsa titre\u015fimi veya ak\u0131\u015f a\u00e7\u0131s\u0131n\u0131 ayarlay\u0131n.<\/p>

5.2.8: \u00c7al\u0131\u015ft\u0131rma \u00f6ncesi onay i\u00e7in \u00dcretim Sorumlusunu aray\u0131n.<\/p>

5.3 Kaps\u00fcl Sayma \u0130\u015flemi<\/b><\/strong><\/h3>

5.3.1: Tabletleri veya kaps\u00fclleri hazneye yava\u015f\u00e7a d\u00f6k\u00fcn. A\u015f\u0131r\u0131 doldurmaktan ka\u00e7\u0131n\u0131n.<\/p>

5.3.2: S\u00fcrekli ve istikrarl\u0131 bir ak\u0131\u015f sa\u011flay\u0131n.<\/p>

5.3.3: Onaylanan ayarlara g\u00f6re sayma i\u015flemine ba\u015flay\u0131n.<\/p>

5.3.4: G\u00f6zlemleyin:<\/p>

5.3.4.1: Kaps\u00fcllerin ak\u0131\u015f\u0131<\/p>

5.3.4.2: Sens\u00f6r performans\u0131<\/p>

5.3.4.3: \u015ei\u015fe hizalamas\u0131<\/p>

5.3.4.4: Say\u0131m tutarl\u0131l\u0131\u011f\u0131<\/p>

5.3.5: A\u015fa\u011f\u0131daki durumlarda makineyi derhal durdurun:<\/p>

5.3.5.1: S\u0131k\u0131\u015fma meydana geliyor<\/p>

5.3.5.2: Kaps\u00fcller veya tabletler yerinden oynuyor veya \u00e7ift say\u0131l\u0131yor<\/p>

5.3.5.3: Hizalama hatas\u0131 g\u00f6r\u00fcl\u00fcyor<\/p>

5.3.6: Devam etmeden \u00f6nce sorunu d\u00fczeltin.<\/p>

5.3.7: T\u00fcm parti tamamlanana kadar i\u015fleme devam edin.<\/p>

5.4 S\u00fcre\u00e7 \u0130\u00e7i Do\u011frulama<\/b><\/strong><\/h3>

5.4.1: D\u00fczenli aral\u0131klarla (BMR'ye g\u00f6re) saya\u00e7 do\u011frulamas\u0131 ger\u00e7ekle\u015ftirin.<\/p>

5.4.2: Dolu kaplar\u0131 rastgele se\u00e7in.<\/p>

5.4.3: Say\u0131mlar\u0131 a\u015fa\u011f\u0131daki y\u00f6ntemlerden biriyle do\u011frulay\u0131n:<\/p>

5.4.3.1: Manuel say\u0131m<\/p>

5.4.3.2: Ortalama kaps\u00fcl a\u011f\u0131rl\u0131\u011f\u0131 kullan\u0131larak a\u011f\u0131rl\u0131k kontrol\u00fc<\/p>

5.4.4: Uyumsuzluk bulunursa:<\/p>

5.4.4.1: Makineyi durdurun<\/p>

5.4.4.2: Etkilenen kaplar\u0131 izole edin<\/p>

5.4.4.3: Say\u0131m\u0131 tekrarlay\u0131n ve sorunu d\u00fczeltin<\/p>

5.4.5: Sonu\u00e7lar\u0131 hemen BMR'ye kaydedin.<\/p>

5.4.6: K\u00fc\u00e7\u00fck bir de\u011fi\u015fikli\u011fi bile g\u00f6z ard\u0131 etmeyin.<\/p>

5.5 Belgeleme Gereksinimleri<\/b><\/strong><\/h3>

5.5.1: T\u00fcm makine parametrelerini, kontrolleri, d\u00fczeltmeleri ve say\u0131mlar\u0131 \u015furaya kaydedin:<\/p>

5.5.1.1: BMR<\/p>

5.5.1.2: Ekipman kay\u0131t defteri<\/p>

5.5.1.3: Proses i\u00e7i kontrol formu<\/p>

5.5.2: Belgeleme, faaliyetin yap\u0131ld\u0131\u011f\u0131 anda yap\u0131lmal\u0131d\u0131r, daha sonra de\u011fil.<\/p>

5.5.3: Kay\u0131t:<\/p>

5.5.3.1: Makine ayarlar\u0131<\/p>

5.5.3.2: Toplam kaps\u00fcl say\u0131s\u0131<\/p>

5.5.3.3: Reddedilenler<\/p>

5.5.3.4: Yap\u0131lan herhangi bir ayarlama<\/p>

5.5.3.5: Operat\u00f6r\u00fcn ba\u015f harfleri, tarih ve saat<\/p>

5.5.4: \u201cYaz\u0131l\u0131 olmayan, yap\u0131lmam\u0131\u015f say\u0131l\u0131r.\u201d<\/p>

5.6 Operasyon Sonras\u0131 Temizlik ve Kapatma<\/b><\/strong><\/h3>

5.6.1: Makineyi kapat\u0131n.<\/p>

5.6.2: Hazneden, oluktan ve tepsilerden kalan t\u00fcm kaps\u00fclleri \u00e7\u0131kar\u0131n.<\/p>

5.6.3: Temas eden par\u00e7alar\u0131 dikkatlice s\u00f6k\u00fcn.<\/p>

5.6.4: Her par\u00e7ay\u0131 onaylanm\u0131\u015f temizlik malzemeleri kullanarak temizleyin.<\/p>

5.6.5: T\u00fcm toz, kal\u0131nt\u0131 ve kal\u0131nt\u0131lar\u0131 temizleyin.<\/p>

5.6.6: Makine y\u00fczeylerini t\u00fcy b\u0131rakmayan bir bezle silin.<\/p>

5.6.7: D\u00f6k\u00fclen kaps\u00fclleri veya kal\u0131nt\u0131lar\u0131 temizlemek i\u00e7in \u00e7evreyi temizleyin.<\/p>

5.6.8: Hat temizleme i\u015flemini ger\u00e7ekle\u015ftirin ve belgeleyin.<\/p>

5.6.9: Ekipman temizleme kay\u0131t defterini imzalay\u0131n, a\u015fa\u011f\u0131dakiler dahil:<\/p>

5.6.9.1: Parti numaras\u0131<\/p>

5.6.9.2: \u00dcr\u00fcn ad\u0131<\/p>

5.6.9.3: Temizlik tarihi ve saati<\/p>

5.6.9.4: Operat\u00f6r\u00fcn ba\u015f harfleri<\/p>

5.6.10: Makineyi teslim etmeden \u00f6nce, denet\u00e7i ve kalite kontrol sorumlusu temizli\u011fi do\u011frulamal\u0131d\u0131r.<\/p>

6.0 Kabul Kriterleri<\/b><\/strong><\/h2>

6.0.1: T\u00fcm kaplar, BMR'ye g\u00f6re tam olarak belirtilen say\u0131da kaps\u00fcl i\u00e7ermelidir.<\/p>

6.0.2: \u00c7apraz bula\u015fma veya kar\u0131\u015f\u0131kl\u0131k yok.<\/p>

6.0.3: Eksiksiz, do\u011fru ve ger\u00e7ek zamanl\u0131 dok\u00fcmantasyon.<\/p>

6.0.4: Serbest b\u0131rakmadan \u00f6nce makineyi kal\u0131nt\u0131 kalmayacak \u015fekilde temizleyin.<\/p>

7.0 Tan\u0131mlar<\/b><\/strong><\/h2>

7.0.1: BMR<\/b><\/strong>Partiye \u00f6zel talimatlar\u0131 i\u00e7eren Parti \u00dcretim Kayd\u0131.<\/p>

7.0.2: Kaps\u00fcl Sayac\u0131<\/b><\/strong>Kaps\u00fclleri say\u0131p kaplara yerle\u015ftirmek i\u00e7in kullan\u0131lan bir makine.<\/p>

7.0.3:\u00a0Hat Temizli\u011fi<\/b><\/strong>\u00d6nceki partiden kalan hi\u00e7bir malzemenin alanda kalmamas\u0131n\u0131 sa\u011flama s\u00fcreci.<\/p>

7.0.4:\u00a0\u0130\u015flemdeki \u00c7ek<\/b><\/strong>\u0130\u015flem s\u0131ras\u0131nda do\u011fruluk ve uyumlulu\u011fu sa\u011flamak i\u00e7in do\u011frulama yap\u0131l\u0131r.<\/p>

Kaps\u00fcl Say\u0131m Prosed\u00fcr\u00fc (SOP) PDF dosyas\u0131n\u0131 \u00fccretsiz indirin.<\/b><\/strong><\/h2>

Kaps\u00fcl Sayac\u0131 Standart \u0130\u015flem Prosed\u00fcr\u00fc (SOP) PDF dosyas\u0131n\u0131 indirin.<\/i><\/b><\/u><\/em><\/strong><\/a><\/p>

Haz\u0131rlad\u0131\u011f\u0131m\u0131z Kaps\u00fcl Say\u0131m Prosed\u00fcr\u00fc (SOP) PDF'si, \u00fcretim sahas\u0131ndaki operat\u00f6rler i\u00e7in tasarlanm\u0131\u015f, kullan\u0131ma haz\u0131r bir formdur. Bu, operat\u00f6rlerin her ad\u0131m\u0131n GMP standartlar\u0131na tam olarak uygun \u015fekilde y\u00fcr\u00fct\u00fcld\u00fc\u011f\u00fcn\u00fc h\u0131zl\u0131 bir \u015fekilde do\u011frulayabilece\u011fi anlam\u0131na gelir.<\/p>

Do\u011fru Standart \u0130\u015flem Prosed\u00fcr\u00fc (SOP), Do\u011fru Makineyle \u00c7al\u0131\u015f\u0131r<\/b><\/strong><\/h2>

Kaps\u00fcl say\u0131m cihaz\u0131 i\u00e7in bir standart i\u015fletim prosed\u00fcr\u00fc (SOP), yap\u0131 sa\u011flar, hatalar\u0131 azalt\u0131r ve tesisinizden \u00e7\u0131kan her birimin uyumlu olmas\u0131n\u0131 garanti eder. Bununla birlikte, sahip oldu\u011funuz makinenin do\u011fru \u00e7al\u0131\u015fmas\u0131 ve tutarl\u0131 performans sa\u011flamas\u0131 son derece \u00f6nemlidir.<\/p>

Bu ancak Finetech gibi do\u011fru orta\u011f\u0131 se\u00e7ti\u011finizde m\u00fcmk\u00fcn olur. 30 y\u0131l\u0131 a\u015fk\u0131n s\u00fcredir ila\u00e7 end\u00fcstrisine y\u00fcksek kaliteli ekipman tedarik ediyoruz.<\/p>

Bizim kaps\u00fcl sayma makineleri<\/u><\/a>\u00a0Finetech, \u00f6zellikle say\u0131m do\u011frulu\u011fu, sorunsuz kaps\u00fcl ak\u0131\u015f\u0131 ve partiler aras\u0131nda h\u0131zl\u0131 ge\u00e7i\u015fler i\u00e7in tasarlanm\u0131\u015ft\u0131r. Finetech ile, say\u0131m i\u015fleminizi her zaman basit ve do\u011fru tutan ekipmanlara sahip olursunuz.<\/p>

An\u0131nda fiyat teklifi al\u0131n<\/i><\/u><\/em><\/a>\u00a0hemen!<\/i><\/em><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>","protected":false},"excerpt":{"rendered":"

A capsule counter SOP document is a GMP requirement that controls how capsule counting must be performed in a pharmaceutical […]<\/p>\n","protected":false},"author":1,"featured_media":8745,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[88],"tags":[],"class_list":["post-8743","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-pills-counting-machine-resources"],"acf":[],"_links":{"self":[{"href":"https:\/\/pharmamachinecn.com\/tr\/wp-json\/wp\/v2\/posts\/8743","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pharmamachinecn.com\/tr\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/pharmamachinecn.com\/tr\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/pharmamachinecn.com\/tr\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/pharmamachinecn.com\/tr\/wp-json\/wp\/v2\/comments?post=8743"}],"version-history":[{"count":10,"href":"https:\/\/pharmamachinecn.com\/tr\/wp-json\/wp\/v2\/posts\/8743\/revisions"}],"predecessor-version":[{"id":8759,"href":"https:\/\/pharmamachinecn.com\/tr\/wp-json\/wp\/v2\/posts\/8743\/revisions\/8759"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/pharmamachinecn.com\/tr\/wp-json\/wp\/v2\/media\/8745"}],"wp:attachment":[{"href":"https:\/\/pharmamachinecn.com\/tr\/wp-json\/wp\/v2\/media?parent=8743"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/pharmamachinecn.com\/tr\/wp-json\/wp\/v2\/categories?post=8743"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/pharmamachinecn.com\/tr\/wp-json\/wp\/v2\/tags?post=8743"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}