FDF / DRUG PRODUCTS in APAC

Our facility provides best-in-class manufacturing of tablets and ampoules, English and Japanese outstanding customer service, and has more than 330 high skilled...

Japan APAC

FDF / DRUG PRODUCTS in APAC

Our facility provides best-in-class manufacturing of tablets and ampoules, English and Japanese outstanding customer service, and has more than 330 high skilled...

FDF / DRUG PRODUCTS  in APAC

About the plant

Adragos Kawagoe is our cutting-edge manufacturing and end-to-end production facility located at the north west of Tokyo with a strategic location that aligns with the heartbeat of pharmaceutical innovation in Japan. 

Oral Solids: Tablets

Technology:

Granulation and compression of tablets

Uncoated / Film-coated /Orally Dissolving Tablets (ODT) / Double-Layer Tablets

Capacity:

Tableting: 2 billion per year

Packaging: 2 billion per year

Sterile Liquids: Ampoules

Technology:

Terminal sterilization

1 fully automatic filling line

Capacity:

Batch size up to 900 liters

30 million per year

From 1ml to 30ml


Certifications
  • EMA (EU GMP)
  • FDA (cGMP)
  • PMDA/MHLW (Japan GMP)

Activity
  • Oral solids / OSD, Injectables, Tablets, Terminal sterilization, Glass ampoules, FDF / DRUG PRODUCTS manufacturing

Features
  • Uses: Commercial (Phase IV), Human
  • Toxicity (OEB classification): 1 / low-hazard (PDE > 5,000 µg/day), 2 (PDE = 1,000 - 5,000 µg/day), 3 (PDE = 100 - 1,000 µg/day)
  • DEA: Schedule II (high potential for abuse / medical use), Schedule III (lower potential for abuse), Schedule IV (low potential for abuse), Schedule V (lowest potential for abuse)
  • BSL:
  • Therapeutic areas: N/A
  • Markets: FDA (USA), EMA (EU), PMDA (Japan), CDSCO (India), Health Canada (Canada), MHRA (UK), TGA (Australia), NMPA (China), EDE (UAE), ANVISA (Brazil), ANMAT (Argentina), MFDS (South Korea), SFDA (Saudi Arabia)

Batch Size / Reactor
  • Large

Services
  • Regulatory services, Development services, Manufacturing services, Analytical / QC services, Quality Assurance services, Packaging, Logistics, Stability studies design, Stability studies execution, ICH Stability studies, Batch records, Analytical methods development, Analytical methods validation, Release testing of raw materials, Release testing of product, Bioanalysis, Analytical methods transfer, Batch certification / release, GMP documentation, Primary packaging, Secondary packaging, Storage, Distribution, CMC regulatory support

Contact us

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