عرض 5 مرافق
إيطاليا
Adare Pharma | EU
Adare Pharma Solutions
تقدم شركة CDMO العالمية تطوير المنتجات الجاهزة من خلال خبرة التصنيع التجارية، مع التركيز على أشكال الجرعات عن طريق الفم.
Markets: DIGEMID (Peru), ANMAT (Argentina), EDE (UAE), ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), Russian Health Authorities, EMA (EU), COFEPRIS (Mexico), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)
Batch Size: Small, Medium, Large
Therapeutic Areas of Expertise (ATC): (R) Respiratory system, (V01) Allergens, (M) Musculoskeletal system, (J) Antiinfectives for systemic use, (C) Cardiovascular system, (A) Digestive tract and metabolism, (N) Nervous system
Category / Product: FDF / DRUG PRODUCTS, SERVICES, PARTICLE ENGINEERING
Compliance: EMA (EU GMP), PMDA/MHLW (Japan GMP), UAE Ministry of Health & Prevention, ANVISA (Brazil B-GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), French Service-Public (CIR), TGA (Australia GMP), FDA (cGMP), NMPA (China GMP), ECOVADIS, ISO, Halal Research Council, Health Canada (Canada GMP), TITCK (Turkish Health Authorities), MFDS/KFDA (Republic of Korea GMP)
Region: Europe
Use: Human, Veterinary
Services: Analytical / QC services, Logistics, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services
OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 5,000 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 1 / low-hazard (PDE > 5,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)
الولايات المتحدة
Adare Pharma | US
Adare Pharma Solutions
Adare Pharma هي شركة CDMO عالمية يتم تركيبها على EE.UU. والاتحاد الأوروبي، الذي يوفر تطوير المنتجات يدويًا عبر الخبرة في مجال التصنيع التجاري
Markets: DIGEMID (Peru), ANMAT (Argentina), EDE (UAE), ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), Russian Health Authorities, EMA (EU), COFEPRIS (Mexico), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)
Batch Size: Small, Medium, Large
Category / Product: FDF / DRUG PRODUCTS, SERVICES, PARTICLE ENGINEERING
Compliance: EMA (EU GMP), PMDA/MHLW (Japan GMP), UAE Ministry of Health & Prevention, ANVISA (Brazil B-GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), French Service-Public (CIR), TGA (Australia GMP), FDA (cGMP), NMPA (China GMP), ECOVADIS, ISO, Halal Research Council, Health Canada (Canada GMP), TITCK (Turkish Health Authorities), MFDS/KFDA (Republic of Korea GMP)
Use: Human, Veterinary
Services: Analytical / QC services, Logistics, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services
OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 5,000 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 1 / low-hazard (PDE > 5,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)
Region: North America
Therapeutic Areas of Expertise (ATC): (C) Cardiovascular system, (A) Digestive tract and metabolism
أيرلندا
Aenova Group - Location Killorglin, Ireland
Aenova
مركز مختص لتجفيف الرش وكريات الإطلاق المعدلة.
Batch Size: Small, Medium, Large
Category / Product: FDF / DRUG PRODUCTS, PARTICLE ENGINEERING, NUTRACEUTICALS
Compliance: EMA (EU GMP), PMDA/MHLW (Japan GMP), SFDA (Saudi Food & Drug Authority), ISO, MFDS/KFDA (Republic of Korea GMP)
Region: Europe
Use: Human, Veterinary
Services: Analytical / QC services, Manufacturing services, Development services, Packaging, Quality Assurance services
Markets: PMDA (Japan), EMA (EU), MFDS (South Korea), SFDA (Saudi Arabia)
OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 5,000 µg/day), 1 / low-hazard (PDE > 5,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)
إسبانيا
PHARMALOOP S.L. - a Salvat Company
Laboratorios Salvat
حلول CDMO متكاملة تمامًا للتعبئة بالنفخ (BFS)، والجرعات المتعددة المعقمة، والجرعات المتعددة غير المعقمة، والأكياس، والكبسولات والأقراص.
Batch Size: Small, Medium, Large
Category / Product: FDF / DRUG PRODUCTS, PARTICLE ENGINEERING
Compliance: EMA (EU GMP), FDA (cGMP), ISO
Region: Europe
Use: Human
Services: Analytical / QC services, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services
Markets: FDA (USA), EMA (EU)
Therapeutic Areas of Expertise (ATC): (V01) Allergens, (S) Sensory organs
BSL (Biological Safety Level): 1
OEB (Occupational Exposure Banding): 1 / low-hazard (PDE > 5,000 µg/day)
عرض محدود
FDF / DRUG PRODUCTS manufacturing site
MAI network supplier
GMP CDMO الموثوق به لتصنيع منتجات الأدوية الصيدلانية المعقمة وغير المعقمة المتقدمة، وتطوير التركيبات، والاختبارات التحليلية.
الموقع متاح بعد التسجيل
النتائج المقترحة
تتوافق هذه المرافق مع معاييرك الرئيسية ولكن ليس جميع المرشحات الاختيارية.
عرض محدود
FDF / DRUG PRODUCTS manufacturing site
MAI network supplier
منشأة تصنيع وسيطة وواجهة برمجة التطبيقات (API) معتمدة من إدارة الغذاء والدواء الأمريكية (USFDA).
الموقع متاح بعد التسجيل
عرض محدود
PARTICLE ENGINEERING manufacturing site
MAI network supplier
واجهة برمجة التطبيقات (API) والشركة المصنعة المتوسطة الحاصلة على شهادات عالمية.
الموقع متاح بعد التسجيل
عرض محدود
FDF / DRUG PRODUCTS manufacturing site
MAI network supplier
منشأة كيميائية وصيدلانية
الموقع متاح بعد التسجيل
عرض محدود
FDF / DRUG PRODUCTS manufacturing site
MAI network supplier
محطة استنشاق المسحوق الجاف.
الموقع متاح بعد التسجيل
عرض محدود
FDF / DRUG PRODUCTS manufacturing site
MAI network supplier
منشأة لتصنيع الجرعات الصلبة عن طريق الفم (OSD) على نطاق تجاري تتمتع بخبرة قوية في المواد الخاضعة للرقابة (DEA II V).
الموقع متاح بعد التسجيل
عرض محدود
FDF / DRUG PRODUCTS manufacturing site
MAI network supplier
منشأة تصنيع تعاقدية متخصصة في الجرعات الصلبة عن طريق الفم (OSD) للإمدادات السريرية والتجارية.
الموقع متاح بعد التسجيل
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