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TCI's GMP

Three advantages of TCI’s GMP

1) More than 20 years of FDA Approved, GMP manufacturing experience

2) Our experiences of many reagents allows us to handle a wide variety of compounds

    We can propose process development for scale-up
    We can research and develop to meet your target timelines and price.


3) Our experts will proactively discuss your project with you.
 

GMP corresponding range

From research and discovery to ingredients of clinical trial for human

Discovery Select candidates Preclinical Clinical Trial for Human Approved and Marketed New Drugs Expired Patent
P1 P2a P2b P3
TCI’s Availability
We can comply with your requests from research and discovery to synthesis of candidate compounds and scale-up of ingredients for pre-clinical development and clinical trials.
 

GMP facility

GMP Facility (Opened in 2017), GMP Kilolab (Opened in 2016)

GMP Factory

Exclusive manufacturing facility for custom synthesis of ingredients for clinical trials

 
Size 1,034 m2 (height 25 m)
Floor levels 4
Bay series 2 + (+1 more in the future)
Reactors 200 L × 2 (GL)
500L × 1 (GL)
800L × 1 (GL)
Crystallization Apparatus 500 L × 1 (SUS)
1,000L × 1 (GL)
Corresponding Temperature -15~120℃
(Cold・Hot Water, Brine, Steam)
Centrifuge 2 (Teflon・SUS)
Conical Dryer 2 (GL)
Purification Water Apparatus Production Capacity 800 L/h

GMP Kilolab (Operation has started in October, 2016)

GMP Kilolab

- Clean Room (Class 100k) 2 rooms
- Draft Chambers in each room
- Multi Kilolab Unit 25L 1 unit introduced
- Air Shower Apparatus

Exclusive manufacturing facility for pharmaceutical ingredient

- Clean room of "class 100,000"    - Booth of "class 100,000"    - Repacking room

  
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