
Batch Size: Small, Medium
Region: North America

Lifecore Biomedical
CDMO que fabrica medicamentos injetáveis estéreis clínicos e comerciais.
Batch Size: Large, Small, Medium
Use: Human, Veterinary
BSL (Biological Safety Level): 1, 2, 3
Compliance: ISO, FDA (cGMP), ANVISA (Brazil B-GMP), TGA (Australia GMP), ECOVADIS, EMA (EU GMP), Health Canada (Canada GMP), MFDS/KFDA (Republic of Korea GMP)
Markets: FDA (USA), EMA (EU), PMDA (Japan), NMPA (China), Health Canada (Canada), ANVISA (Brazil), ISP (Chile), MSPAS (Guatemala), COFEPRIS (Mexico), DIGEMID (Peru), MHRA (UK), Russian Health Authorities, CDSCO (India), MFDS (South Korea), Turkish Health Authorities, EDE (UAE), SFDA (Saudi Arabia), ANMAT (Argentina), INVIMA (Colombia), TGA (Australia), Resto do mundo
Services: Development services, Logistics, Analytical / QC services, Manufacturing services, Quality Assurance services, Regulatory services, Packaging
Controlled Substances: Lowest potential for abuse
OEB (Occupational Exposure Banding): 3 (PDE = 100 - 1,000 µg/day), 1 / low-hazard (PDE > 5,000 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 2 (PDE = 1,000 - 5,000 µg/day)
Category / Product: FDF / DRUG PRODUCTS
Region: North America

Adare Pharma Solutions
Adare Pharma é um CDMO global com instalações em EE.UU. e na UE, que oferece desenvolvimento de produtos manualmente com base na experiência de fabricação comer
Services: Development services, Logistics, Analytical / QC services, Packaging, Regulatory services, Quality Assurance services, Manufacturing services
Markets: EMA (EU), PMDA (Japan), NMPA (China), FDA (USA), Health Canada (Canada), ANVISA (Brazil), ISP (Chile), MSPAS (Guatemala), COFEPRIS (Mexico), DIGEMID (Peru), Russian Health Authorities, MHRA (UK), ANMAT (Argentina), INVIMA (Colombia), SFDA (Saudi Arabia), MFDS (South Korea), EDE (UAE), TGA (Australia)
Compliance: FDA (cGMP), ISO, PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), Halal Research Council, ECOVADIS, TGA (Australia GMP), TITCK (Turkish Health Authorities), UAE Ministry of Health & Prevention, French Service-Public (CIR), NMPA (China GMP), EMA (EU GMP), Health Canada (Canada GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), MFDS/KFDA (Republic of Korea GMP)
Use: Human, Veterinary
Batch Size: Large, Small, Medium
OEB (Occupational Exposure Banding): 3 (PDE = 100 - 1,000 µg/day), 1 / low-hazard (PDE > 5,000 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 2 (PDE = 1,000 - 5,000 µg/day)
Category / Product: FDF / DRUG PRODUCTS, PARTICLE ENGINEERING, SERVICES
Therapeutic Areas of Expertise (ATC): (C) Cardiovascular system, (A) Digestive tract and metabolism
Region: North America

Aenova
Centro de Competência Embalagens de Sólidos.
Services: Logistics, Manufacturing services, Packaging
Markets: FDA (USA), Health Canada (Canada)
Compliance: FDA (cGMP), Halal Research Council, Health Canada (Canada GMP), NSF
Batch Size: Large, Small, Medium
Category / Product: NUTRACEUTICALS
Use: Human
Region: North America
MAI network supplier
Organização de Desenvolvimento e Fabricação de Contrato (CDMO) com foco em proteínas recombinantes e anticorpos monoclonais (mAbs).
Localização disponível após o registo
MAI network supplier
Sterile injectables: formulation development, clinical and commercial manufacturing. Approvals: USFDA, PMDA.
Localização disponível após o registo
MAI network supplier
Oral solids, creams, liquids and ointments: formulation development, clinical and commercial manufacturing. Approvals: USFDA, EMA.
Localização disponível após o registo
Estas instalações correspondem aos seus critérios principais, mas nem todos os filtros opcionais.
MAI network supplier
CRO/CMO farmacêutico
Localização disponível após o registo
MAI network supplier
Desenvolvimento de API, fabricação clínica e comercial. Aprovações: USFDA, PMDA.
Localização disponível após o registo
MAI network supplier
Plataforma CDMO avançada para APIs de pequenas moléculas altamente complexas, Guayama, Porto Rico. VISÃO GERAL Skalar Pharma opera um dos fabricantes de API mai
Localização disponível após o registo
MAI network supplier
QUALIDADE E EXCELÊNCIA REGULATÓRIA • Alinhado com FDA cGMP (21 CFR Partes 210 e 211) • Operações em conformidade com ICH Q7 • Sistema abrangente de gerenciament
Localização disponível após o registo
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