
Adare Pharma Solutions
Adare Pharma es un CDMO global con instalaciones en EE.UU. y la UE, que ofrece desarrollo de productos llave en mano mediante experiencia en fabricación comerci
MÄRKTE: 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-GRÖSSE: Klein, Mittel, Groß
KATEGORIE/PRODUKT: FDF/DROGENPRODUKTE, DIENSTLEISTUNGEN, CHEMISCH-SYNTHETISCH
COMPLIANCE: EMA (EU-GMP), PMDA/MHLW (Japan GMP), UAE Ministry of Health & Prevention, ANVISA (Brazil B-GMP), Weltgesundheitsorganisation (GMP / HACCP), MHRA (UK GMP), Französischer Dienst - öffentlich (CIR), TGA (Australia GMP), FDA (cGMP), NMPA (China GMP), ECOVADIS, ISO, Halal-Forschungsrat, Gesundheit Kanada (Kanada GMP), TITCK (Turkish Health Authorities), MFDS/KFDA (Republik Korea GMP)
REGION: Europe, North America
VERWENDUNG: Menschlich, Veterinär
DIENSTLEISTUNGEN: 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/Tag), 4 / HPAPI (PDE = 10 - 100 µg/Tag), 1 / low-hazard (PDE > 5,000 µg/day), 3 (PDE = 100 - 1.000 µg/Tag)
THERAPEUTISCHE FACHGEBIETE (ATC): (C) Cardiovascular system, (A) Digestive tract and metabolism, (D) Dermatologicals

Adare Pharma Solutions
Global CDMO offering turnkey product development through commercial manufacturing expertise, focused on oral dosage forms.
MÄRKTE: 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-GRÖSSE: Klein, Mittel, Groß
THERAPEUTISCHE FACHGEBIETE (ATC): (R) Respiratory system, (V01) Allergens, (M) Musculoskeletal system, (J) Antiinfectives for systemic use, (C) Cardiovascular system, (A) Digestive tract and metabolism, (D) Dermatologicals, (N) Nervous system
KATEGORIE/PRODUKT: FDF/DROGENPRODUKTE, DIENSTLEISTUNGEN, PARTIKELTECHNIK, CHEMISCH-SYNTHETISCH
COMPLIANCE: EMA (EU-GMP), PMDA/MHLW (Japan GMP), UAE Ministry of Health & Prevention, ANVISA (Brazil B-GMP), Weltgesundheitsorganisation (GMP / HACCP), MHRA (UK GMP), Französischer Dienst - öffentlich (CIR), TGA (Australia GMP), FDA (cGMP), NMPA (China GMP), ECOVADIS, ISO, Halal-Forschungsrat, Gesundheit Kanada (Kanada GMP), TITCK (Turkish Health Authorities), MFDS/KFDA (Republik Korea GMP)
REGION: Europe
VERWENDUNG: Menschlich, Veterinär
DIENSTLEISTUNGEN: 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/Tag), 4 / HPAPI (PDE = 10 - 100 µg/Tag), 1 / low-hazard (PDE > 5,000 µg/day), 3 (PDE = 100 - 1.000 µg/Tag)

Aenova
Centro de competencia y ventanilla única para cápsulas de gelatina blanda y VegaGels.
BATCH-GRÖSSE: Klein, Mittel, Groß
KATEGORIE/PRODUKT: FDF/DROGENPRODUKTE, NUTRAZEUTIKA, CHEMISCH-SYNTHETISCH
COMPLIANCE: EMA (EU-GMP), TGA (Australia GMP), FDA (cGMP), ISO, Halal-Forschungsrat, Gesundheit Kanada (Kanada GMP)
REGION: Europe
VERWENDUNG: Menschlich
DIENSTLEISTUNGEN: Analytical / QC services, Manufacturing services, Development services, Packaging, Quality Assurance services
OEB (Occupational Exposure Banding): 2 (PDE = 1.000 - 5.000 µg/Tag), 1 / low-hazard (PDE > 5,000 µg/day), 3 (PDE = 100 - 1.000 µg/Tag)
MÄRKTE: FDA (USA), TGA (Australia), Health Canada (Canada)
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Desarrollador y fabricante de nuevos medicamentos con tecnologías de liberación controlada.
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