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CDMO Business Model

Pre-IND/

Development

Phase I clinical trials/Pilot
Phase II clinical trials/Process
Phase III clinical trials/Validation
Launch
Our recently opened state of the art R&D facility is home to over 150 R&D chemists who utilize the latest techniques in organic chemistry and purification technologies.
Our innovative chemists develop cost effective, safe, novel routes to intermediates enabling a smooth transition when processes are transferred to our FDA inspected manufacturing facility. We support customers intermediates in Pre-IND, Phase I, Phase II, Phase III and Launch stages.
Regular communication is maintained throughout the duration of the project to allow customers to follow the progress, and stay up to date with developments.
Finally, upon completion of each project a comprehensive campaign report is provided.
Service

Customized service

Efficient production / project management

Positive communication and updates

Quotation

Quality & cost-driven process innovation​

Established technology platforms

Efficient evaluation, costing and quotation system​

Delivery

On time and full delivery of in-specification products​

Active after-sale service

EHS

Effective safety management system​s

Green production concept

Sustainability / Social responsibility​

Enquiry to project rate is >70%.

More than 5,000 enquiries received.

Projects with top 20 global pharmaceutical companies.

Providing commercialized product to >50% of them.​

CDMO Project Experience

40% of revenue from CDMO business.

In FY 2022, revenue increased by 50% compared with 2021.

More than 95% of projects successfully delivered, with >90% delivered on time and in full.  Low rate of customer complaints.

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Commercial products

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Products enter Phase III drug

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 Products enter Phase I/II drugs

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Products enter Preclinical drugs

CDMO Project Experience
Project Management
Customer Support
Procedure
Resources Management
Cost Management 
Production Management
1. Evaluation, project establishment and closure
2. Project follow-up / update / communication
3. Support with related documents
4. Coordinate related departments
1. Develop project procedure
2. Assign project task
3. Project Timeline Control
1. Collect project requirements
2. Equipment procurement
3. Coordinate / allocate resources
1. Cost assessment
2. Cost control
1.Coordinate R&D / plant
2.Coordinate production plan
3.Control production progress
Our Advantages

Broad technology platforms with

​intellectual property protection.

More than 15 years’ experience in

​CDMO business, 

cost-efficient synthetic route design.

Manufacturing site with first class quality systems, 

integrated supply chain, continuous production capacity​.

Commercial production of a wide range of chiral alcohols, α- and β-amino acids, chiral amines and heterocyclic compounds.

Evaluation from a US based customer: 

"​One of the best advanced intermediate

​manufacturing sites in China".

Striving for superior quality and EHS, 

excellent customer service and communication