Cerca e trova il CMO / CDMO di cui hai bisogno
Discover highly skilled partners for your drug development and manufacturing project.
Stati Uniti
Adare Pharma | US
Adare Pharma Solutions
Adare Pharma è un CDMO globale con installazioni in EE.UU. e l'UE, che offre lo sviluppo di prodotti da lasciare in mano grazie all'esperienza nella fabbricazio
MERCATI: 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)
DIMENSIONE DEL LOTTO: Piccolo, Medio, Grande
CATEGORIA / PRODOTTO: FDF / DRUG PRODUCTS, SERVICES, PARTICLE ENGINEERING
COMPLIANCE: EMA (GMP UE), PMDA/MHLW (Japan GMP), UAE Ministry of Health & Prevention, ANVISA (Brazil B-GMP), Organizzazione Mondiale della Sanità (GMP / HACCP), MHRA (UK GMP), Servizio pubblico francese (CIR), TGA (Australia GMP), FDA (cGMP), NMPA (Cina GMP), ECOVADIS, ISO, Consiglio di ricerca halal, Health Canada (Canada GMP), TITCK (Turkish Health Authorities), MFDS/KFDA (Repubblica di Corea GMP)
USO: Umano, Veterinario
SERVIZI: Analytical / QC services, Logistics, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services
OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/giorno), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1.000 µg/giorno)
REGIONE: North America
AREE TERAPEUTICHE DI COMPETENZA (ATC): (C) Cardiovascular system, (A) Digestive tract and metabolism
Italia
Adare Pharma | EU
Adare Pharma Solutions
CDMO globale offre sviluppo di prodotti chiavi in mano attraverso competenze di produzione commerciale, focalizzate su forme di dosaggio orali.
MERCATI: 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)
DIMENSIONE DEL LOTTO: Piccolo, Medio, Grande
AREE TERAPEUTICHE DI COMPETENZA (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
CATEGORIA / PRODOTTO: FDF / DRUG PRODUCTS, SERVICES, PARTICLE ENGINEERING
COMPLIANCE: EMA (GMP UE), PMDA/MHLW (Japan GMP), UAE Ministry of Health & Prevention, ANVISA (Brazil B-GMP), Organizzazione Mondiale della Sanità (GMP / HACCP), MHRA (UK GMP), Servizio pubblico francese (CIR), TGA (Australia GMP), FDA (cGMP), NMPA (Cina GMP), ECOVADIS, ISO, Consiglio di ricerca halal, Health Canada (Canada GMP), TITCK (Turkish Health Authorities), MFDS/KFDA (Repubblica di Corea GMP)
REGIONE: Europe
USO: Umano, Veterinario
SERVIZI: Analytical / QC services, Logistics, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services
OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/giorno), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1.000 µg/giorno)
Spagna
PHARMALOOP S.L. - a Salvat Company
Laboratorios Salvat
Soluzioni CDMO completamente integrate per Blow-Fill-Seal (BFS), multidose sterile, multidose non sterile, bustine, capsule e compresse.
DIMENSIONE DEL LOTTO: Piccolo, Medio, Grande
CATEGORIA / PRODOTTO: FDF / DRUG PRODUCTS, PARTICLE ENGINEERING
COMPLIANCE: EMA (GMP UE), FDA (cGMP), ISO
REGIONE: Europe
USO: Umano
SERVIZI: Analytical / QC services, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services
MERCATI: FDA (USA), EMA (EU)
AREE TERAPEUTICHE DI COMPETENZA (ATC): (V01) Allergens, (S) Sensory organs
BSL (Livello di sicurezza biologica): 1
OEB (Occupational Exposure Banding): 1 / low-hazard (PDE > 10,000 µg/day)
Limited view
FDF / DRUG PRODUCTS manufacturing site
MAI network supplier
Il tuo CDMO GMP di fiducia per la produzione avanzata di prodotti farmaceutici asettici e non asettici, lo sviluppo di formulazioni e test analitici.
Location available after registration
Suggested Results
These facilities match your main criteria but not all optional filters.
Limited view
PARTICLE ENGINEERING manufacturing site
MAI network supplier
Un produttore API e intermedio con certificazioni globali.
Location available after registration
Limited view
FDF / DRUG PRODUCTS manufacturing site
MAI network supplier
Impianto per inalazione di polvere secca.
Location available after registration
Limited view
FDF / DRUG PRODUCTS manufacturing site
MAI network supplier
Impianto Chimico-Farmaceutico
Location available after registration
Limited view
FDF / DRUG PRODUCTS manufacturing site
MAI network supplier
Una struttura API e produzione intermedia approvata dalla USFDA.
Location available after registration
Stati Uniti
Avara Pharmaceutical Services | Arecibo Site
AVARA
Impianto di produzione di dosaggi solidi orali (OSD) su scala commerciale con una forte esperienza nelle sostanze controllate (DEA II V).
DIMENSIONE DEL LOTTO: Medio, Grande
AREE TERAPEUTICHE DI COMPETENZA (ATC): (R) Respiratory system, (H) Systemic hormonal preparations excl. sex hormones and insulins, (M) Musculoskeletal system, (L) Antineoplastic and immunomodulating agents, (S) Sensory organs, (G) Genito urinary system and sex hormones, (J) Antiinfectives for systemic use, (C) Cardiovascular system, (A) Digestive tract and metabolism, (N) Nervous system, (B) Blood and blood forming organs
CATEGORIA / PRODOTTO: FDF / DRUG PRODUCTS, SERVICES, PARTICLE ENGINEERING, CHEMICAL-SYNTHETIC
COMPLIANCE: Roszdravnadzor (Russia GMP), EMA (GMP UE), PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), FDA (cGMP), Health Canada (Canada GMP), MFDS/KFDA (Repubblica di Corea GMP), ICH
SOSTANZE CONTROLLATE: Lowest potential for abuse, High potential for abuse & medical use, Lower potential for abuse, Low potential for abuse
MERCATI: ANVISA (Brazil), PMDA (Japan), FDA (USA), Russian Health Authorities, EMA (EU), MFDS (South Korea), TGA (Australia), Health Canada (Canada)
USO: Umano
SERVIZI: Analytical / QC services, Manufacturing services, Packaging, Quality Assurance services
OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1.000 µg/giorno)
REGIONE: North America
Stati Uniti
Avara Pharmaceutical Services | Norman Site
AVARA
Impianto di produzione a contratto specializzato nel dosaggio solido orale (OSD) per la fornitura clinica e commerciale.
DIMENSIONE DEL LOTTO: Piccolo, Medio, Grande
AREE TERAPEUTICHE DI COMPETENZA (ATC): (R) Respiratory system, (H) Systemic hormonal preparations excl. sex hormones and insulins, (M) Musculoskeletal system, (L) Antineoplastic and immunomodulating agents, (S) Sensory organs, (G) Genito urinary system and sex hormones, (J) Antiinfectives for systemic use, (C) Cardiovascular system, (A) Digestive tract and metabolism, (N) Nervous system, (B) Blood and blood forming organs
CATEGORIA / PRODOTTO: FDF / DRUG PRODUCTS, SERVICES, PARTICLE ENGINEERING, CHEMICAL-SYNTHETIC
COMPLIANCE: Roszdravnadzor (Russia GMP), EMA (GMP UE), PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), MHRA (UK GMP), TGA (Australia GMP), FDA (cGMP), Health Canada (Canada GMP), MFDS/KFDA (Repubblica di Corea GMP), ICH
SOSTANZE CONTROLLATE: Lowest potential for abuse, High potential for abuse & medical use, Lower potential for abuse, Low potential for abuse
MERCATI: ANVISA (Brazil), PMDA (Japan), FDA (USA), Russian Health Authorities, EMA (EU), MFDS (South Korea), TGA (Australia), Health Canada (Canada), MHRA (UK)
USO: Umano
SERVIZI: Analytical / QC services, Manufacturing services, Development services, Packaging, Quality Assurance services
OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1.000 µg/giorno)
REGIONE: North America