跳到主要内容
联系我们

药筒灌装 CDMO 公司
注射筒制造服务

您值得信赖的注射盒制造和开发合作伙伴

显示中 21 设施
Lifecore Injectables CDMO
美国

Lifecore Injectables CDMO

Lifecore Biomedical

生产临床和商业无菌注射药品的 CDMO。

市场: DIGEMID (Peru), ANMAT (Argentina), Turkish Health Authorities, EDE (UAE), 世界其他地区, ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), CDSCO (India), 俄罗斯卫生当局, EMA (EU), COFEPRIS (Mexico), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)

批量大小: 小的, 中等的, 大的

类别/产品: FDF / 药品

遵守: EMA (EU GMP), ANVISA (Brazil B-GMP), TGA (Australia GMP), FDA (cGMP), ECOVADIS, ISO, Health Canada (Canada GMP), MFDS/KFDA (Republic of Korea GMP)

受控物质: 滥用可能性最低

BSL(生物安全等级): 3, 1, 2

使用: 人类, 兽医

服务: 分析/质量控制服务, 后勤, 制造服务, 监管服务, 开发服务, 包装, 质量保证服务

OEB(职业暴露带): 2(PDE = 1,000 - 10,000 微克/天), 4 / HPAPI(PDE = 10 - 100 微克/天), 1 / 低危害(PDE > 10,000 µg/天), 3(PDE = 100 - 1,000 微克/天)

地区: 北美

EVER Pharma Jena GmbH
德国

EVER Pharma Jena GmbH

EVER Neuro Pharma GmbH

用于开发和生产小分子注射剂的专业 CDMO。

市场: DIGEMID (Peru), ANMAT (Argentina), Turkish Health Authorities, EDE (UAE), 世界其他地区, ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), CDSCO (India), 俄罗斯卫生当局, EMA (EU), COFEPRIS (Mexico), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)

批量大小: 小的, 中等的, 大的

类别/产品: FDF / 药品

遵守: Roszdravnadzor (Russia GMP), EMA (EU GMP), PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), NMPA (China GMP), ISO, TITCK (Turkish Health Authorities), MFDS/KFDA (Republic of Korea GMP)

受控物质: 滥用可能性最低, 滥用和医疗用途的可能性很高, 降低滥用的可能性, 滥用可能性低

地区: 欧洲

使用: 人类

服务: 分析/质量控制服务, 后勤, 制造服务, 监管服务, 开发服务, 包装, 质量保证服务

专业治疗领域 (ATC): (H) 全身性激素制剂,不包括。性激素和胰岛素, (L) 抗肿瘤药和免疫调节剂, (N) 神经系统

OEB(职业暴露带): 2(PDE = 1,000 - 10,000 微克/天), 5 / HPAPI(PDE < 10 微克/天), 4 / HPAPI(PDE = 10 - 100 微克/天), 1 / 低危害(PDE > 10,000 µg/天), 3(PDE = 100 - 1,000 微克/天)

BSL(生物安全等级): 1, 2

Aenova Group - Location Latina, Italy
意大利

Aenova Group - Location Latina, Italy

Aenova

动物保健产品和无菌技术能力中心。

市场: Turkish Health Authorities, ANVISA (Brazil), FDA (USA), 俄罗斯卫生当局, EMA (EU), SFDA (Saudi Arabia)

批量大小: 小的, 中等的, 大的

类别/产品: FDF / 药品

遵守: Roszdravnadzor (Russia GMP), EMA (EU GMP), ANVISA (Brazil B-GMP), FDA (cGMP), SFDA (Saudi Food & Drug Authority), TITCK (Turkish Health Authorities)

地区: 欧洲

使用: 人类, 兽医

服务: 分析/质量控制服务, 后勤, 制造服务, 监管服务, 开发服务, 包装, 质量保证服务

OEB(职业暴露带): 2(PDE = 1,000 - 10,000 微克/天), 1 / 低危害(PDE > 10,000 µg/天), 3(PDE = 100 - 1,000 微克/天)

BSL(生物安全等级): 1, 2

GENSENTA ILAC SANAYI AS
土耳其

GENSENTA ILAC SANAYI AS

GENSENTA

CMO & CDMO & FDF 制造商

市场: Turkish Health Authorities, ANVISA (Brazil), PMDA (Japan), FDA (USA), 俄罗斯卫生当局, EMA (EU), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), Health Canada (Canada), MHRA (UK)

批量大小: 小的, 中等的, 大的

类别/产品: FDF / 药品, 服务

遵守: Roszdravnadzor (Russia GMP), EMA (EU GMP), PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), MHRA (UK GMP), TGA (Australia GMP), SFDA (Saudi Food & Drug Authority), Health Canada (Canada GMP), TITCK (Turkish Health Authorities), MFDS/KFDA (Republic of Korea GMP)

受控物质: 滥用可能性最低, 滥用和医疗用途的可能性很高, 降低滥用的可能性, 滥用可能性低

地区: 欧洲

使用: 人类

服务: 分析/质量控制服务, 制造服务, 开发服务, 包装, 质量保证服务

OEB(职业暴露带): 2(PDE = 1,000 - 10,000 微克/天), 4 / HPAPI(PDE = 10 - 100 微克/天), 1 / 低危害(PDE > 10,000 µg/天), 3(PDE = 100 - 1,000 微克/天)

专业治疗领域 (ATC): (M) 肌肉骨骼系统, (J) 全身使用的抗感染药, (三) 心血管系统, (A) 消化道和新陈代谢, (D) 皮肤科, (N) 神经系统, (P) 抗寄生虫产品、杀虫剂和驱虫剂

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

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

Seacross Pharmaceutical Co Ltd

研发中心在支持原料药和成品剂型的开发方面发挥着基础性作用。

市场: DIGEMID (Peru), ANMAT (Argentina), Turkish Health Authorities, EDE (UAE), 世界其他地区, ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), CDSCO (India), 俄罗斯卫生当局, EMA (EU), COFEPRIS (Mexico), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)

批量大小: 小的, 中等的, 大的

专业治疗领域 (ATC): (R) 呼吸系统, (V09-10)放射性药物, (H) 全身性激素制剂,不包括。性激素和胰岛素, (V01) 过敏原, (M) 肌肉骨骼系统, (L) 抗肿瘤药和免疫调节剂, (V04)诊断剂, (S) 感觉器官, (G) Genito泌尿系统和性激素, (J) 全身使用的抗感染药, (三) 心血管系统, (A) 消化道和新陈代谢, (D) 皮肤科, (N) 神经系统, (P) 抗寄生虫产品、杀虫剂和驱虫剂, (B) 血液和造血器官, (V06) 营养素

类别/产品: FDF / 药品, 化学合成

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

受控物质: 滥用可能性最低, 滥用可能性高且无医疗用途, 滥用和医疗用途的可能性很高, 降低滥用的可能性, 滥用可能性低

BSL(生物安全等级): 3, 4, 1, 2

使用: 人类

服务: 分析/质量控制服务, 后勤, 制造服务, 监管服务, 开发服务, 包装, 质量保证服务

地区: 亚太地区

OEB(职业暴露带): 2(PDE = 1,000 - 10,000 微克/天), 5 / HPAPI(PDE < 10 微克/天), 4 / HPAPI(PDE = 10 - 100 微克/天), 1 / 低危害(PDE > 10,000 µg/天), 3(PDE = 100 - 1,000 微克/天)

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

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

Seacross Pharmaceutical Co Ltd

制剂生产基地致力于复杂、高价值剂型的开发和生产。

市场: DIGEMID (Peru), ANMAT (Argentina), Turkish Health Authorities, EDE (UAE), 世界其他地区, ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), CDSCO (India), 俄罗斯卫生当局, EMA (EU), COFEPRIS (Mexico), MFDS (South Korea), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)

批量大小: 小的, 中等的, 大的

专业治疗领域 (ATC): (R) 呼吸系统, (H) 全身性激素制剂,不包括。性激素和胰岛素, (V01) 过敏原, (M) 肌肉骨骼系统, (L) 抗肿瘤药和免疫调节剂, (V04)诊断剂, (S) 感觉器官, (G) Genito泌尿系统和性激素, (J) 全身使用的抗感染药, (三) 心血管系统, (A) 消化道和新陈代谢, (D) 皮肤科, (N) 神经系统, (P) 抗寄生虫产品、杀虫剂和驱虫剂, (B) 血液和造血器官, (V06) 营养素

类别/产品: FDF / 药品, 服务

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

受控物质: 滥用可能性最低, 滥用可能性高且无医疗用途, 滥用和医疗用途的可能性很高, 降低滥用的可能性, 滥用可能性低

BSL(生物安全等级): 3, 4, 1, 2

使用: 人类

服务: 分析/质量控制服务, 后勤, 制造服务, 监管服务, 开发服务, 包装, 质量保证服务

地区: 亚太地区

OEB(职业暴露带): 2(PDE = 1,000 - 10,000 微克/天), 5 / HPAPI(PDE < 10 微克/天), 4 / HPAPI(PDE = 10 - 100 微克/天), 1 / 低危害(PDE > 10,000 µg/天), 3(PDE = 100 - 1,000 微克/天)

Cenexi Laboratoires Thissen
比利时

Cenexi Laboratoires Thissen

Cenexi

这家工厂占地 8,000 平方米,占地近 7 公顷,建筑物星罗棋布,位于布鲁塞尔以南 20 公里处,拥有 340 名员工*。

批量大小: 小的, 中等的, 大的

类别/产品: FDF / 药品

遵守: EMA (EU GMP), PMDA/MHLW (Japan GMP), ANVISA (Brazil B-GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), TGA (Australia GMP), FDA (cGMP), NMPA (China GMP), Health Canada (Canada GMP), MFDS/KFDA (Republic of Korea GMP)

受控物质: 滥用可能性最低, 滥用和医疗用途的可能性很高, 降低滥用的可能性, 滥用可能性低

地区: 欧洲

BSL(生物安全等级): 3, 4, 1, 2

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

使用: 人类, 兽医

服务: 分析/质量控制服务, 制造服务, 监管服务, 开发服务, 包装, 质量保证服务

专业治疗领域 (ATC): (H) 全身性激素制剂,不包括。性激素和胰岛素, (L) 抗肿瘤药和免疫调节剂, (G) Genito泌尿系统和性激素

OEB(职业暴露带): 2(PDE = 1,000 - 10,000 微克/天), 5 / HPAPI(PDE < 10 微克/天), 4 / HPAPI(PDE = 10 - 100 微克/天), 1 / 低危害(PDE > 10,000 µg/天), 3(PDE = 100 - 1,000 微克/天)

视野有限

FDF / 药品 manufacturing site

MAI network supplier

全球生物综合服务 CDMO

注册后可用位置

视野有限

FDF / 药品 manufacturing site

MAI network supplier

专门用于 GMP 配方和无菌液体注射剂无菌灌装的灌装和加工场地。

注册后可用位置

视野有限

FDF / 药品 manufacturing site

MAI network supplier

端到端制药 CDMO

注册后可用位置

建议结果

这些设施符合您的主要标准,但不符合所有可选过滤器。

HIPRA BIOTECH SERVICES | Amer
西班牙

HIPRA BIOTECH SERVICES | Amer

HIPRA Biotech Services

从细胞系开发到商业制造的端到端内部能力。

市场: DIGEMID (Peru), ANMAT (Argentina), ANVISA (Brazil), ISP (Chile), PMDA (Japan), FDA (USA), MSPAS (Guatemala), EMA (EU), COFEPRIS (Mexico), Health Canada (Canada), INVIMA (Colombia), MHRA (UK)

批量大小: 小的, 中等的, 大的

类别/产品: FDF / 药品, 生物制剂

遵守: ISP (Chile BPM), ANMAT (Argentina nueva GMP), EMA (EU GMP), PMDA/MHLW (Japan GMP), DIGEMID, ANVISA (Brazil B-GMP), World Health Organization (GMP / HACCP), MHRA (UK GMP), FDA (cGMP), ISO, INVIMA, Health Canada (Canada GMP), MSPAS, COFEPRIS

地区: 欧洲

使用: 人类, 兽医

服务: 分析/质量控制服务, 后勤, 制造服务, 监管服务, 开发服务, 包装, 质量保证服务

OEB(职业暴露带): 2(PDE = 1,000 - 10,000 微克/天), 1 / 低危害(PDE > 10,000 µg/天), 3(PDE = 100 - 1,000 微克/天)

BSL(生物安全等级): 1, 2

HBM Pharma
斯洛伐克

HBM Pharma

Hbm Pharma

经欧盟 GMP 认证的 CMO,总部位于斯洛伐克马丁。该公司为无菌药品提供制造和包装服务。产品和固体口服剂型

市场: Turkish Health Authorities, ANVISA (Brazil), 俄罗斯卫生当局, EMA (EU), COFEPRIS (Mexico), SFDA (Saudi Arabia), TGA (Australia), NMPA (China), Health Canada (Canada), MHRA (UK)

批量大小: 小的, 中等的, 大的

类别/产品: FDF / 药品, 服务

遵守: Roszdravnadzor (Russia GMP), EMA (EU GMP), UAE Ministry of Health & Prevention, ANVISA (Brazil), TGA (Australia GMP), NMPA (China GMP), ECOVADIS, ISO, Health Canada (Canada GMP)

地区: 欧洲

使用: 人类

服务: 分析/质量控制服务, 制造服务, 包装, 质量保证服务

OEB(职业暴露带): 2(PDE = 1,000 - 10,000 微克/天), 1 / 低危害(PDE > 10,000 µg/天), 3(PDE = 100 - 1,000 微克/天)

受控物质: 滥用和医疗用途的可能性很高

网络上有更多设施

注册即可解锁完整目录,其中包含联系方式和地点。

+11 更多设施

创建免费帐户

Cartridges are a key format for injectable drug delivery — especially in combination products like insulin pens, autoinjectors, and multi-dose delivery systems. Their precision, user convenience, and compatibility with self-administration devices make them ideal for chronic therapies. To meet strict quality and regulatory standards, pharma and biotech innovators rely on specialized cartridge filling CDMO companies.

With full-service injectable cartridge manufacturing, these CDMOs offer formulation, aseptic filling, device integration, and packaging support under global GMP conditions.

How to Choose Cartridge Filling CDMO Companies

When selecting among cartridge filling CDMO companies, important factors include:

  • Sterile fill-finish capabilities in ISO 5 environments (RABS/isolators)
  • Device compatibility with 1.5 mL, 3 mL, and custom cartridge sizes
  • Handling of high-viscosity or sensitive biologics
  • Support for dual-chamber and lyophilized formats
  • Cold chain and high-containment infrastructure, if needed
  • Track record with combination products and regulatory support for DMF, NDA, and CE filings
  • Integrated labeling, serialization, and packaging

A qualified CDMO ensures your cartridge product meets clinical, technical, and commercial goals.

Key Services Offered by Injectable Cartridge Manufacturing Partners

Top-tier providers of injectable cartridge manufacturing services typically include:

  • Formulation development tailored to cartridge systems
  • GMP aseptic filling of glass or polymer cartridges
  • Stopper insertion, plunger assembly, and crimping
  • Labeling, visual inspection, and serialization
  • Container closure integrity testing (CCIT)
  • Lyophilization and dual-chamber filling, if applicable
  • Stability studies under ICH guidelines
  • Regulatory support for combination product and drug filings

These services are critical for therapies in diabetes, hormone replacement, ophthalmology, and rare diseases.

Advantages of Partnering with Cartridge Filling CDMO Companies

Working with expert cartridge filling CDMO companies offers several benefits:

  • Device-ready output for autoinjectors, pens, and reusable systems
  • Reduced time to market with integrated fill-finish workflows
  • Improved patient compliance via convenient formats
  • Regulatory alignment with combination product experience
  • Consistent quality in aseptic filling and device assembly

A capable CDMO helps streamline your injectable program from formulation through final device integration.

Cartridge Filling CDMO Companies

Some of the most trusted cartridge filling CDMO companies include:

  • EVER Neuro Pharma GmbH: Specialized CDMO for the development and production of small-molecule injectables. [See CDMO profile]
  • GENSENTA: CMO, CDMO and FDF manufacturer. [See CDMO profile]
  • HIPRA Biotech Services: End-to-end internal capabilities from cell line development to commercial manufacturing. [See CDMO profile]
  • Hbm Pharma: Manufacturing and packaging services for sterile pharmaceutical products and solid oral dosage forms. [See CDMO profile]
  • BAG Health Care GmbH: Parenteral fill & finish provider for vials in small to mid-sized batches. [See CDMO profile]
  • CZ Vaccines: Commercial-scale manufacturing facility. [See CDMO profile]
  • Green Phoenix Labs GmbH: GMP manufacturing and QP batch release for cell and tissue therapies. [See CDMO profile]
  • LABORATORIO REIG JOFRE SA: State-of-the-art facilities for the development and manufacturing of betalactam antibiotics (FDF). [See CDMO profile]
  • Grifols International: Sterile manufacturing solutions for small molecules in flexible bags and vials. [See CDMO profile]
  • Adragos Pharma: Aseptic fill & finish manufacturing of lyophilized or liquid sterile (bio)pharmaceutical drug products. [See CDMO profile]
  • Seda Pharma Development Services Ltd: Specializes in integrated pharmaceutical development and clinical pharmacology. [See CDMO profile]
  • STE PRASFARMA: CMO/CDMO specializing in cytostatics and high-potency products. [See CDMO profile]
  • Sichuan Huiyu Pharmaceuticals: Specialized in CMO/CDMO services for APIs and complex injectables, including cartridge manufacturing. [See CDMO profile]
  • Cenexi: Injectables manufacturing. [See CDMO profile]
  • ASCIL Biopharm: A GMP facility fully equipped for R&D and pharmaceutical development. Includes laboratories and a pilot plant for technical and clinical batches of sterile products. [See CDMO profile]
  • White Raven: Fill & finish site dedicated to GMP formulation and aseptic filling of sterile liquid injectables, including cartridge manufacturing. [See CDMO profile]
  • Ascendia Pharmaceutical Solutions: GMP-certified CDMO providing advanced sterile and non-sterile pharmaceutical manufacturing, formulation development, and analytical testing services. [See CDMO profile]
  • Aenova Group: Competence center specializing in conventional solid dosage forms and clinical services, as well as semisolids and liquid pharmaceutical products. [See CDMO profile]
  • Lifecore Injectables CDMO: Clinical and commercial manufacturing of sterile injectable drug products. [See CDMO profile]

Related Information

Let MAI CDMO Help You Find the Right Cartridge Filling CDMO Partner

At MAI CDMO, we connect pharma and biotech companies with top-tier cartridge filling CDMO companies offering full-service injectable cartridge manufacturing solutions. Whether you’re developing a new combination product or scaling an approved injectable, our network ensures you find the right partner to meet your technical and commercial needs.

Looking to outsource sterile cartridge production? Contact us today and let’s match you with the ideal CDMO.