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貴社の医薬品開発および製造プロジェクトのための高度なスキルを持つパートナーを見つけてください。

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Adragos Pharma | Livron
フランス

Adragos Pharma | Livron

Adragos Pharma

無菌の液体および座薬の製造。当社は 100 を超える分子、麻薬管理、分析および安定性サービスを扱います。

OEB (職業性暴露バンディング): 5 / HPAPI (PDE < 10 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day)

規制物質: 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

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

サービス: Logistics, Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

地域: ヨーロッパ

バッチサイズ: Large, Small, Medium

使用: Human

コンプライアンス: EMA (EU GMP), MFDS/KFDA (Republic of Korea GMP)

カテゴリ / 製品: FDF / 医薬品

Glatt Pharmaceutical Services GmbH Co. & KG
ドイツ

Glatt Pharmaceutical Services GmbH Co. & KG

Glatt Pharmaceutical Services GmbH Co. & KG

ドイツのビンゼンに拠点を置く、複雑な経口固形剤形分野におけるエンドツーエンドのサービスを提供する cGMP 準拠の CDMO。

規制物質: 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

市場: EMA (EU), FDA (USA)

地域: ヨーロッパ

コンプライアンス: FDA (cGMP), EMA (EU GMP)

バッチサイズ: Large, Small, Medium

使用: Human, Veterinary

BSL (生物学的安全性レベル): 1

サービス: Development services, Manufacturing services, Analytical / QC services

治療専門分野 (ATC): (C) Cardiovascular system, (H) Systemic hormonal preparations excl. sex hormones and insulins, (J) Antiinfectives for systemic use, (L) Antineoplastic and immunomodulating agents, (M) Musculoskeletal system, (N) Nervous system, (R) Respiratory system, (S) Sensory organs, (V06) Nutrients, (B) Blood and blood forming organs, (A) Digestive tract and metabolism

OEB (職業性暴露バンディング): 4 / HPAPI (PDE = 10 - 100 µg/day), 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day)

カテゴリ / 製品: FDF / 医薬品

Adare Pharma | US
アメリカ合衆国

Adare Pharma | US

Adare Pharma Solutions

Adare Pharma es un CDMO global con instalaciones en EE.UU. UE では、製品の開発と製造の中間体験を行っています。

市場: 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)

サービス: Logistics, Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

コンプライアンス: 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)

バッチサイズ: Large, Small, Medium

使用: Human, Veterinary

治療専門分野 (ATC): (C) Cardiovascular system, (A) Digestive tract and metabolism

OEB (職業性暴露バンディング): 4 / HPAPI (PDE = 10 - 100 µg/day), 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day)

地域: 北米

カテゴリ / 製品: サービス, FDF / 医薬品, 粒子工学

Adare Pharma | EU
イタリア

Adare Pharma | EU

Adare Pharma Solutions

グローバル CDMO は、経口剤形に焦点を当てた商業製造の専門知識を通じてターンキー製品開発を提供します。

治療専門分野 (ATC): (A) Digestive tract and metabolism, (C) Cardiovascular system, (J) Antiinfectives for systemic use, (M) Musculoskeletal system, (N) Nervous system, (R) Respiratory system, (V01) Allergens

市場: TGA (Australia), 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)

コンプライアンス: 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), 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

バッチサイズ: Small, Medium, Large

OEB (職業性暴露バンディング): 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day)

カテゴリ / 製品: サービス, FDF / 医薬品, 粒子工学

サービス: Logistics, Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

地域: ヨーロッパ

使用: Human, Veterinary

Green Phoenix Labs GmbH
ドイツ

Green Phoenix Labs GmbH

Green Phoenix Labs GmbH

過剰なクリーンルーム能力を持つ細胞治療会社。

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

規制物質: Lowest potential for abuse, Low potential for abuse, Lower potential for abuse

バッチサイズ: Small, Medium

OEB (職業性暴露バンディング): 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day)

コンプライアンス: EMA (EU GMP)

カテゴリ / 製品: 生物製剤, サービス, FDF / 医薬品

市場: EMA (EU)

サービス: Logistics, Development services, Manufacturing services, Quality Assurance services, Regulatory services, Packaging

地域: ヨーロッパ

使用: Human

BSL (生物学的安全性レベル): 1

Seda Pharma Development Services
イギリス

Seda Pharma Development Services

Seda Pharma Development Services Ltd

Seda 医薬品開発サービスは、統合された医薬品開発と臨床薬理学を専門としています。

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

市場: TGA (Australia), Rest of World, 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), Turkish Health Authorities, EDE (UAE), CDSCO (India)

バッチサイズ: Small, Medium

OEB (職業性暴露バンディング): 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day), 5 / HPAPI (PDE < 10 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day)

コンプライアンス: MHRA (UK GMP), ECOVADIS

カテゴリ / 製品: FDF / 医薬品

地域: ヨーロッパ

使用: Human

サービス: Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

Sichuan Huiyu Pharmaceuticals Co., Ltd. - API Manufacturing Site
中国

Sichuan Huiyu Pharmaceuticals Co., Ltd. - API Manufacturing Site

Seacross Pharmaceutical Co Ltd

当社の API 製造施設は、研究開発センターおよび製剤工場と並ぶ 3 つの中核拠点の 1 つとして、統合されたサプライ チェーンにおいて重要な役割を果たしています。

規制物質: 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

市場: 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), Turkish Health Authorities, EDE (UAE), CDSCO (India), TGA (Australia), Rest of World

サービス: Logistics, Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

地域: アジア太平洋

コンプライアンス: DIGEMID, BRCGS, FDA (cGMP), ISO, PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), MSPAS, COFEPRIS, Roszdravnadzor (Russia GMP), IFS, Halal Research Council, ECOVADIS, TGA (Australia GMP), TITCK (Turkish Health Authorities), UAE Ministry of Health & Prevention, SFDA (Saudi Food & Drug Authority), INVIMA, ISP (Chile BPM), French Service-Public (CIR), NMPA (China GMP), ANMAT (Argentina nueva GMP), EMA (EU GMP), Health Canada (Canada GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), MFDS/KFDA (Republic of Korea GMP), SQF (Safe Quality Food), NSF

バッチサイズ: Large, Small, Medium

使用: Human

BSL (生物学的安全性レベル): 1, 2, 3, 4

カテゴリ / 製品: 化学合成品

治療専門分野 (ATC): (C) Cardiovascular system, (D) Dermatologicals, (H) Systemic hormonal preparations excl. sex hormones and insulins, (J) Antiinfectives for systemic use, (L) Antineoplastic and immunomodulating agents, (M) Musculoskeletal system, (N) Nervous system, (P) Antiparasitic products, insecticides and repellents, (R) Respiratory system, (S) Sensory organs, (V01) Allergens, (V06) Nutrients, (V09-10) Radiopharmaceuticals, (B) Blood and blood forming organs, (A) Digestive tract and metabolism, (G) Genito urinary system and sex hormones, (V04) Diagnostic agents

OEB (職業性暴露バンディング): 4 / HPAPI (PDE = 10 - 100 µg/day), 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day), 5 / HPAPI (PDE < 10 µg/day)

Sichuan Huiyu Pharmaceuticals Co., Ltd. - R&D Site
中国

Sichuan Huiyu Pharmaceuticals Co., Ltd. - R&D Site

Seacross Pharmaceutical Co Ltd

R&D センターは、API と最終剤形の両方の開発をサポートする上で基本的な役割を果たします。

コンプライアンス: MFDS/KFDA (Republic of Korea GMP), SQF (Safe Quality Food), NSF, DIGEMID, BRCGS, FDA (cGMP), ISO, PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), MSPAS, COFEPRIS, Roszdravnadzor (Russia GMP), IFS, Halal Research Council, ECOVADIS, TGA (Australia GMP), TITCK (Turkish Health Authorities), UAE Ministry of Health & Prevention, SFDA (Saudi Food & Drug Authority), INVIMA, ISP (Chile BPM), French Service-Public (CIR), NMPA (China GMP), ANMAT (Argentina nueva GMP), EMA (EU GMP), Health Canada (Canada GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP)

カテゴリ / 製品: FDF / 医薬品, 化学合成品

OEB (職業性暴露バンディング): 1 / low-hazard (PDE > 10,000 µg/day), 5 / HPAPI (PDE < 10 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)

治療専門分野 (ATC): (V04) Diagnostic agents, (C) Cardiovascular system, (D) Dermatologicals, (H) Systemic hormonal preparations excl. sex hormones and insulins, (J) Antiinfectives for systemic use, (L) Antineoplastic and immunomodulating agents, (M) Musculoskeletal system, (N) Nervous system, (P) Antiparasitic products, insecticides and repellents, (R) Respiratory system, (S) Sensory organs, (V01) Allergens, (V06) Nutrients, (V09-10) Radiopharmaceuticals, (B) Blood and blood forming organs, (A) Digestive tract and metabolism, (G) Genito urinary system and sex hormones

BSL (生物学的安全性レベル): 3, 4, 1, 2

規制物質: 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

市場: 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), Turkish Health Authorities, EDE (UAE), CDSCO (India), TGA (Australia), Rest of World

サービス: Logistics, Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

地域: アジア太平洋

バッチサイズ: Large, Small, Medium

使用: Human

Sichuan Huiyu Pharmaceuticals Co., Ltd. - Formulation Manufacturing Site
中国

Sichuan Huiyu Pharmaceuticals Co., Ltd. - Formulation Manufacturing Site

Seacross Pharmaceutical Co Ltd

製剤製造サイトは、複雑で高価値の剤形の開発と生産に特化しています。

治療専門分野 (ATC): (V04) Diagnostic agents, (C) Cardiovascular system, (D) Dermatologicals, (H) Systemic hormonal preparations excl. sex hormones and insulins, (J) Antiinfectives for systemic use, (L) Antineoplastic and immunomodulating agents, (M) Musculoskeletal system, (N) Nervous system, (P) Antiparasitic products, insecticides and repellents, (R) Respiratory system, (S) Sensory organs, (V01) Allergens, (V06) Nutrients, (B) Blood and blood forming organs, (A) Digestive tract and metabolism, (G) Genito urinary system and sex hormones

OEB (職業性暴露バンディング): 5 / HPAPI (PDE < 10 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day)

BSL (生物学的安全性レベル): 3, 4, 1, 2

規制物質: 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

市場: 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), Turkish Health Authorities, EDE (UAE), CDSCO (India), TGA (Australia), Rest of World

サービス: Logistics, Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

地域: アジア太平洋

コンプライアンス: DIGEMID, BRCGS, FDA (cGMP), ISO, PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), MSPAS, COFEPRIS, Roszdravnadzor (Russia GMP), IFS, Halal Research Council, ECOVADIS, TGA (Australia GMP), TITCK (Turkish Health Authorities), UAE Ministry of Health & Prevention, SFDA (Saudi Food & Drug Authority), INVIMA, ISP (Chile BPM), French Service-Public (CIR), NMPA (China GMP), ANMAT (Argentina nueva GMP), EMA (EU GMP), Health Canada (Canada GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), MFDS/KFDA (Republic of Korea GMP), SQF (Safe Quality Food), NSF

バッチサイズ: Large, Small, Medium

使用: Human

カテゴリ / 製品: サービス, FDF / 医薬品

PHARMALOOP S.L. - a Salvat Company
スペイン

PHARMALOOP S.L. - a Salvat Company

Laboratorios Salvat

ブローフィルシール (BFS)、滅菌複数回投与、非滅菌複数回投与、サシェ、カプセル、錠剤用の完全に統合された CDMO ソリューション。

市場: EMA (EU), FDA (USA)

地域: ヨーロッパ

コンプライアンス: FDA (cGMP), ISO, EMA (EU GMP)

バッチサイズ: Large, Small, Medium

使用: Human

BSL (生物学的安全性レベル): 1

サービス: Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

治療専門分野 (ATC): (S) Sensory organs, (V01) Allergens

カテゴリ / 製品: FDF / 医薬品, 粒子工学

OEB (職業性暴露バンディング): 1 / low-hazard (PDE > 10,000 µg/day)

Ophtapharm, a Sentiss Company
スイス

Ophtapharm, a Sentiss Company

Ophtapharm, a Sentiss Company

眼科および耳科 - 溶液、懸濁液、乳濁液、軟膏およびゲル - FDA 承認施設。

市場: EMA (EU), FDA (USA)

地域: ヨーロッパ

コンプライアンス: FDA (cGMP), ISO, EMA (EU GMP), World Health Organization (GMP / HACCP)

バッチサイズ: Large, Small, Medium

使用: Human, Veterinary

サービス: Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

カテゴリ / 製品: FDF / 医薬品

Cenexi SAS
フランス

Cenexi SAS

Cenexi

Accueil Sites オスニー。 2011 年に買収された Osny の施設は、高活性固形医薬品の開発と生産を専門としています。

OEB (職業性暴露バンディング): 5 / HPAPI (PDE < 10 µg/day), 4 / HPAPI (PDE = 10 - 100 µg/day), 2 (PDE = 1,000 - 10,000 µg/day), 3 (PDE = 100 - 1,000 µg/day), 1 / low-hazard (PDE > 10,000 µg/day)

市場: EMA (EU), PMDA (Japan), NMPA (China), FDA (USA), ANVISA (Brazil), MHRA (UK), MFDS (South Korea)

地域: ヨーロッパ

コンプライアンス: FDA (cGMP), PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), EMA (EU GMP), MFDS/KFDA (Republic of Korea GMP)

使用: Human

サービス: Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Regulatory services, Packaging

治療専門分野 (ATC): (H) Systemic hormonal preparations excl. sex hormones and insulins, (V01) Allergens, (G) Genito urinary system and sex hormones

バッチサイズ: Small, Medium

カテゴリ / 製品: FDF / 医薬品

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