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Cenexi Hérouville Saint Clair
Frankreich

Cenexi Hérouville Saint Clair

Cenexi

Der Standort Hérouville-Saint-Clair in der Nähe von Caen in der Normandie ist auf die Herstellung und Abfüllung von injizierbaren und nicht injizierbaren steril

KONTROLLIERTE SUBSTANZEN: High potential for abuse & medical use, Lowest potential for abuse, Low potential for abuse, High potential for abuse & no medical use, Lower potential for abuse

MÄRKTE: EMA (EU), PMDA (Japan), NMPA (China), FDA (USA), ANVISA (Brazil), Russian Health Authorities, MHRA (UK), MFDS (South Korea), TGA (Australia)

REGION: Europe

COMPLIANCE: FDA (cGMP), PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), NMPA (China GMP), EMA (EU-GMP), MHRA (UK GMP), MFDS/KFDA (Republik Korea GMP)

VERWENDUNG: Menschlich

DIENSTLEISTUNGEN: Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

THERAPEUTISCHE FACHGEBIETE (ATC): (C) Cardiovascular system, (D) Dermatologicals, (H) Systemic hormonal preparations excl. sex hormones and insulins, (J) Antiinfectives for systemic use, (N) Nervous system, (A) Digestive tract and metabolism

OEB (Occupational Exposure Banding): 4 / HPAPI (PDE = 10 - 100 µg/Tag), 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1.000 µg/Tag), 1 / low-hazard (PDE > 10,000 µg/day)

BATCH-GRÖSSE: Klein, Mittel

KATEGORIE/PRODUKT: FDF / DRUG PRODUCTS

Cenexi Laboratoires Thissen
Belgien

Cenexi Laboratoires Thissen

Cenexi

Das 8.000 m² große Werk mit Gebäuden auf einem fast sieben Hektar großen Gelände liegt 20 km südlich von Brüssel und beschäftigt 340 Mitarbeiter*.

OEB (Occupational Exposure Banding): 5 / HPAPI (PDE < 10 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/Tag), 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1.000 µg/Tag), 1 / low-hazard (PDE > 10,000 µg/day)

BSL (Biologische Sicherheitsstufe): 3, 4, 1, 2

KONTROLLIERTE SUBSTANZEN: High potential for abuse & medical use, Lowest potential for abuse, Low potential for abuse, Lower potential for abuse

MÄRKTE: EMA (EU), PMDA (Japan), NMPA (China), FDA (USA), Health Canada (Canada), ANVISA (Brazil), MHRA (UK), MFDS (South Korea), TGA (Australia)

REGION: Europe

COMPLIANCE: FDA (cGMP), PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), TGA (Australia GMP), NMPA (China GMP), EMA (EU-GMP), Gesundheit Kanada (Kanada GMP), Weltgesundheitsorganisation (GMP / HACCP), MHRA (UK GMP), MFDS/KFDA (Republik Korea GMP)

BATCH-GRÖSSE: Groß, Klein, Mittel

VERWENDUNG: Menschlich, Veterinär

DIENSTLEISTUNGEN: Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

THERAPEUTISCHE FACHGEBIETE (ATC): (H) Systemic hormonal preparations excl. sex hormones and insulins, (L) Antineoplastic and immunomodulating agents, (G) Genito urinary system and sex hormones

KATEGORIE/PRODUKT: FDF / DRUG PRODUCTS

STE PRASFARMA
Spanien

STE PRASFARMA

STE PRASFARMA

CMO/CDMO-Zytostatika und hochwirksame Produkte.

OEB (Occupational Exposure Banding): 5 / HPAPI (PDE < 10 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/Tag)

BSL (Biologische Sicherheitsstufe): 3, 4

KONTROLLIERTE SUBSTANZEN: High potential for abuse & medical use

COMPLIANCE: ICH, ISO, ANVISA (Brazil B-GMP), TITCK (Turkish Health Authorities), SFDA (Saudi Food & Drug Authority), NMPA (China GMP), EMA (EU-GMP)

MÄRKTE: EMA (EU), NMPA (China), ANVISA (Brazil), MHRA (UK), SFDA (Saudi Arabia), Turkish Health Authorities

DIENSTLEISTUNGEN: Logistics, Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

REGION: Europe

BATCH-GRÖSSE: Groß, Klein, Mittel

VERWENDUNG: Menschlich

THERAPEUTISCHE FACHGEBIETE (ATC): (L) Antineoplastic and immunomodulating agents

KATEGORIE/PRODUKT: FDF / DRUG PRODUCTS

Limited view

CHEMICAL-SYNTHETIC manufacturing site

MAI network supplier

Lösungen für nicht virale Lieferprogramme

Location available after registration

Limited view

FDF / DRUG PRODUCTS manufacturing site

MAI network supplier

End-to-End-Pharma-CDMO

Location available after registration

Limited view

SERVICES manufacturing site

MAI network supplier

Flüssige und lyophilisierte Fläschchen – Zwei Annex-I-konforme BSL-2-Reinraumsuiten.

Location available after registration

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Laboratorios Grifols | Murcia Plant
Spanien

Laboratorios Grifols | Murcia Plant

Grifols International

Sterile Herstellungslösungen (kleine Moleküle) in flexiblen Beuteln.

MÄRKTE: ANMAT (Argentina), ANVISA (Brazil), FDA (USA), EMA (EU), MFDS (South Korea), TGA (Australia)

BATCH-GRÖSSE: Klein, Mittel, Groß

KATEGORIE/PRODUKT: FDF / DRUG PRODUCTS

COMPLIANCE: ISP (Chile BPM), ANMAT (Argentinien neue GMP), EMA (EU-GMP), ANVISA (Brazil B-GMP), Weltgesundheitsorganisation (GMP / HACCP), MHRA (UK GMP), TGA (Australia GMP), FDA (cGMP), ECOVADIS, ISO, INVIMA, Gesundheit Kanada (Kanada GMP), MFDS/KFDA (Republik Korea GMP)

KONTROLLIERTE SUBSTANZEN: Lowest potential for abuse, Lower potential for abuse, Low potential for abuse

REGION: Europe

VERWENDUNG: Menschlich, Veterinär

DIENSTLEISTUNGEN: Analytical / QC services, Logistics, 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/Tag)

THERAPEUTISCHE FACHGEBIETE (ATC): (M) Musculoskeletal system, (J) Antiinfectives for systemic use, (C) Cardiovascular system, (A) Digestive tract and metabolism, (N) Nervous system

Adragos Pharma | Halden
Norwegen

Adragos Pharma | Halden

Adragos Pharma

Wir sind auf die Herstellung von Infusionsbeuteln, Kunststoffampullen und Fläschchen mit Blow-Fill-Seal (BFS)-Technologie und anderen Darreichungsformen spezial

MÄRKTE: Turkish Health Authorities, EDE (UAE), ANVISA (Brazil), PMDA (Japan), FDA (USA), EMA (EU), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), MHRA (UK)

BATCH-GRÖSSE: Klein, Mittel, Groß

KATEGORIE/PRODUKT: FDF / DRUG PRODUCTS

COMPLIANCE: EMA (EU-GMP), PMDA/MHLW (Japan GMP), UAE Ministry of Health & Prevention, ANVISA (Brazil B-GMP), Weltgesundheitsorganisation (GMP / HACCP), MHRA (UK GMP), TGA (Australia GMP), FDA (cGMP), NSF, NMPA (China GMP), ISO, TITCK (Turkish Health Authorities), MFDS/KFDA (Republik Korea GMP)

KONTROLLIERTE SUBSTANZEN: Lowest potential for abuse, High potential for abuse & medical use, Lower potential for abuse, Low potential for abuse

REGION: Europe

VERWENDUNG: Menschlich

DIENSTLEISTUNGEN: Analytical / QC services, Logistics, Manufacturing services, Regulatory 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/Tag)

THERAPEUTISCHE FACHGEBIETE (ATC): (A) Digestive tract and metabolism, (D) Dermatologicals, (V06) Nutrients

Adragos Pharma | Kawagoe
Japan

Adragos Pharma | Kawagoe

Adragos Pharma

Unsere Anlage bietet erstklassige Herstellung von Tabletten und Ampullen.

KATEGORIE/PRODUKT: FDF / DRUG PRODUCTS, SERVICES

MÄRKTE: EDE (UAE), PMDA (Japan), FDA (USA), CDSCO (India), EMA (EU), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), Health Canada (Canada), MHRA (UK)

COMPLIANCE: EMA (EU-GMP), PMDA/MHLW (Japan GMP), FDA (cGMP)

BATCH-GRÖSSE: Groß

KONTROLLIERTE SUBSTANZEN: Lowest potential for abuse, High potential for abuse & medical use, Lower potential for abuse, Low potential for abuse

VERWENDUNG: Menschlich

DIENSTLEISTUNGEN: Analytical / QC services, Logistics, Manufacturing services, Regulatory services, Packaging, Quality Assurance services

REGION: APAC

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/Tag)

Adragos Pharma | Livron
Frankreich

Adragos Pharma | Livron

Adragos Pharma

Herstellung von sterilen Flüssigkeiten und Zäpfchen. Wir kümmern uns um mehr als 100 Moleküle, das Betäubungsmittelmanagement sowie Analyse- und Stabilitätsdien

BATCH-GRÖSSE: Klein, Mittel, Groß

KATEGORIE/PRODUKT: FDF / DRUG PRODUCTS

COMPLIANCE: EMA (EU-GMP), MFDS/KFDA (Republik Korea GMP)

KONTROLLIERTE SUBSTANZEN: Lowest potential for abuse, High potential for abuse & no medical use, High potential for abuse & medical use, Lower potential for abuse, Low potential for abuse

REGION: Europe

VERWENDUNG: Menschlich

DIENSTLEISTUNGEN: Analytical / QC services, Logistics, Manufacturing services, Regulatory services, Packaging, Quality Assurance services

MÄRKTE: PMDA (Japan), CDSCO (India), EMA (EU), MFDS (South Korea), TGA (Australia), NMPA (China), MHRA (UK)

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 5 / HPAPI (PDE < 10 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/Tag), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1.000 µg/Tag)

Green Phoenix Labs GmbH
Deutschland

Green Phoenix Labs GmbH

Green Phoenix Labs GmbH

Zelltherapieunternehmen mit überschüssiger Reinraumkapazität.

BATCH-GRÖSSE: Klein, Mittel

THERAPEUTISCHE FACHGEBIETE (ATC): (R) Respiratory system, (M) Musculoskeletal system, (G) Genito urinary system and sex hormones, (C) Cardiovascular system, (A) Digestive tract and metabolism, (D) Dermatologicals, (N) Nervous system, (B) Blood and blood forming organs

KATEGORIE/PRODUKT: FDF / DRUG PRODUCTS, SERVICES, BIOLOGIEN

COMPLIANCE: EMA (EU-GMP)

KONTROLLIERTE SUBSTANZEN: Lowest potential for abuse, Lower potential for abuse, Low potential for abuse

REGION: Europe

VERWENDUNG: Menschlich

DIENSTLEISTUNGEN: Logistics, Manufacturing services, Regulatory 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/Tag)

BSL (Biologische Sicherheitsstufe): 1

MÄRKTE: EMA (EU)

Seda Pharma Development Services
Vereinigtes Königreich

Seda Pharma Development Services

Seda Pharma Development Services Ltd

Seda Pharmaceutical Development Services ist auf integrierte pharmazeutische Entwicklung und klinische Pharmakologie spezialisiert.

MÄRKTE: DIGEMID (Peru), ANMAT (Argentina), Turkish Health Authorities, EDE (UAE), Rest of World, ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), CDSCO (India), 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

KATEGORIE/PRODUKT: FDF / DRUG PRODUCTS

REGION: Europe

VERWENDUNG: Menschlich

COMPLIANCE: MHRA (UK GMP), ECOVADIS

DIENSTLEISTUNGEN: Analytical / QC services, Manufacturing services, Regulatory services, Development services, Packaging, Quality Assurance services

OEB (Occupational Exposure Banding): 2 (PDE = 1,000 - 10,000 µg/day), 5 / HPAPI (PDE < 10 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/Tag), 1 / low-hazard (PDE > 10,000 µg/day), 3 (PDE = 100 - 1.000 µg/Tag)

THERAPEUTISCHE FACHGEBIETE (ATC): (M) Musculoskeletal system, (G) Genito urinary system and sex hormones, (C) Cardiovascular system, (A) Digestive tract and metabolism, (D) Dermatologicals, (N) Nervous system, (B) Blood and blood forming organs

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