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귀하의 약물 개발 및 제조 프로젝트를 위한 고도로 숙련된 파트너를 찾아보세요.

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Adare Pharma | EU
이탈리아

Adare Pharma | EU

Adare Pharma Solutions

경구용 제형에 초점을 맞춘 상업적 제조 전문 지식을 통해 턴키 제품 개발을 제공하는 글로벌 CDMO입니다.

서비스: 개발 서비스, 기호 논리학, 분석/QC 서비스, 포장, 규제 서비스, 품질 보증 서비스, 제조 서비스

시장: EMA (EU), PMDA (Japan), NMPA (China), FDA (USA), Health Canada (Canada), ANVISA (Brazil), ISP (Chile), MSPAS (Guatemala), COFEPRIS (Mexico), DIGEMID (Peru), 러시아 보건 당국, MHRA (UK), ANMAT (Argentina), INVIMA (Colombia), SFDA (Saudi Arabia), MFDS (South Korea), EDE (UAE), TGA (Australia)

규정 준수: 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)

사용: 인간, 수의사

배치 크기: 크기가 큰, 작은, 중간

치료 전문 분야(ATC): (N) 신경계, (J) 전신용 항감염제, (V01) 알레르기 유발물질, (R) 호흡기계, (M) 근골격계, (C) 심혈관계, (A) 소화관 및 대사

OEB(직업 노출 밴딩): 3(PDE = 100 - 1,000μg/일), 1 / 저위험(PDE > 10,000μg/일), 4 / HPAPI(PDE = 10~100μg/일), 2(PDE = 1,000 - 10,000μg/일)

카테고리 / 제품: FDF/의약품, 입자공학, 서비스

지역: 유럽

Adare Pharma | US
미국

Adare Pharma | US

Adare Pharma Solutions

Adare Pharma es un CDMO 글로벌 설치는 EE.UU에 있습니다. y la UE, que ofrece desarrollo de productos llave en mano mediante experiencia en fabricación camerci

서비스: 개발 서비스, 기호 논리학, 분석/QC 서비스, 포장, 규제 서비스, 품질 보증 서비스, 제조 서비스

시장: EMA (EU), PMDA (Japan), NMPA (China), FDA (USA), Health Canada (Canada), ANVISA (Brazil), ISP (Chile), MSPAS (Guatemala), COFEPRIS (Mexico), DIGEMID (Peru), 러시아 보건 당국, MHRA (UK), ANMAT (Argentina), INVIMA (Colombia), SFDA (Saudi Arabia), MFDS (South Korea), EDE (UAE), TGA (Australia)

규정 준수: 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)

사용: 인간, 수의사

배치 크기: 크기가 큰, 작은, 중간

OEB(직업 노출 밴딩): 3(PDE = 100 - 1,000μg/일), 1 / 저위험(PDE > 10,000μg/일), 4 / HPAPI(PDE = 10~100μg/일), 2(PDE = 1,000 - 10,000μg/일)

카테고리 / 제품: FDF/의약품, 입자공학, 서비스

치료 전문 분야(ATC): (C) 심혈관계, (A) 소화관 및 대사

지역: 북아메리카

Aenova Group - Location Cornu, Romania
루마니아

Aenova Group - Location Cornu, Romania

Aenova

연질 젤라틴 캡슐과 VegaGels®에 대한 역량 센터 및 원스톱 매장입니다.

지역: 유럽

시장: FDA (USA), Health Canada (Canada), TGA (Australia)

규정 준수: FDA (cGMP), ISO, Halal Research Council, TGA (Australia GMP), EMA (EU GMP), Health Canada (Canada GMP)

배치 크기: 크기가 큰, 작은, 중간

카테고리 / 제품: 영양식품, FDF/의약품

사용: 인간

서비스: 개발 서비스, 제조 서비스, 분석/QC 서비스, 품질 보증 서비스, 포장

OEB(직업 노출 밴딩): 2(PDE = 1,000 - 10,000μg/일), 3(PDE = 100 - 1,000μg/일), 1 / 저위험(PDE > 10,000μg/일)

제한된 보기

화장품 manufacturing site

MAI network supplier

제어실현 기술을 갖춘 신약 개발 및 제조 업체입니다.

등록 후 이용 가능 위치

제한된 보기

화장품 manufacturing site

MAI network supplier

APl 및 Key 중간체를 위한 원스톱 CDMO 솔루션입니다.

등록 후 이용 가능 위치

제한된 보기

FDF/의약품 manufacturing site

MAI network supplier

제약 및 바이오 산업에 서비스를 제공하는 의약품 개발 및 구강 기술 전달 분야의 프랑스 CDMO 핵심 업체입니다.

등록 후 이용 가능 위치

Are you a pharmaceutical company seeking a reliable CMO or CDMO partner to accelerate your drug development process? Look no further than MAI CDMO Network. Our advanced search platform connects you with a vast network of qualified contract manufacturers and development organizations worldwide.

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  • Create a Free Account: Sign up for a free account to access our extensive database of CMOs and CDMOs.
  • Refine Your Search: Use our advanced search filters to identify providers that meet your exact requirements.
  • Request Quotes: Contact selected providers directly to request quotes and learn more about their services.
  • Make Informed Decisions: Compare quotes, review company profiles, and select the best partner for your project.

Key Benefits of Partnering with a CMO/CDMO

  • Accelerated Time-to-Market: Leverage the expertise and resources of a CMO/CDMO to expedite your drug development process.
  • Reduced Costs: Benefit from economies of scale and specialized equipment to reduce manufacturing costs.
  • Improved Quality: Ensure product quality and compliance with regulatory standards through rigorous quality management systems.
  • Increased Flexibility: Scale up or down production as needed to meet changing market demands.
  • Focus on Core Competencies: Outsource non-core activities to free up internal resources for innovation and strategic initiatives.

Featured Services

  • API Manufacturing: Source high-quality active pharmaceutical ingredients from experienced manufacturers.
  • Clinical Trial Supplies: Secure reliable and compliant supplies for your clinical trials.
  • Fill-Finish and Packaging: Partner with experts in sterile filling, lyophilization, and packaging to ensure product stability and patient safety.
  • Analytical Testing: Access a wide range of analytical services to support your drug development program.

Ready to Find Your Ideal CMO/CDMO Partner? Register Now

Explore our platform today and discover how MAI CDMO Network can help you achieve your drug development goals.