八戒体育(中国)有限公司官网

Partnering

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Internationalization

Globalization as one of the CF PharmTech strategies is being pursued to improve people's respiratory health. By working closely with global partners, the products are going to be registered in different countries or regions, for example in the US, EU, Middle East, South America and other areas.

01

Compliance with GMP requirements and other relevant regulations is not compromised to ensure product quality.
02

We focus on updating standards and regulations to ensure that the quality system and product remain consistently high quality.
03

CF's RA is able to support global registration, including the US, EU and other markets.

One-stop service

CF PHARMTECH dedicated to building a comprehensive and integrated R&D platform and offering partners a CDMO service for inhalation products.

01

Advanced Equipment

The Pharmaceutical Research Institute is located in the Wuxi Airport Industrial Park, and is equipped with nearly 100 instruments for inhalation product research and testing, including a multistage impactor (ACI, NGI), breathing simulators, high-flow vacuum pumps, automatic high-performance liquid chromatography, laser diffraction particle size analyzer, SprayVIEW spray pattern and plume geometry.
02

Production Capacity

The production facility is located in Xiangcheng Economic Development Zone, Suzhou, and is equipped with six advanced production lines for manufacturing various forms of inhalation dosage forms, including inhalation aerosols, nasal sprays, inhalation solutions and inhalation powders. The QC laboratory meets the requirements of China, the EU and the US. Our manufacturing expertise and technical solutions to overcome manufacturing challenges can contribute to your success.
03

Registration system

CF's RA is able to support worldwide registration, including the US, EU and other markets. We can also provide registration service if you are interested.

Provide what you want

R&D Services

Feasibility Study
Formulation Development
Analytical Method Development
Packaging Material/Device Screening
Process Development
CMO Services

Feasibility Study Batch
Preclinical Study Batch
Pilot Batch
Validation/Clinical Batch
Commercial Batch
Other Services

Method Development and Testing
In vitro Testing
Compatibility Study
Stability Study
Submission and Registration