Product Informations
Name: Cabazitaxel
CAS number: 183133-96-2
Chemical formula: C45H57NO14
Specifications: 99%
Color: white or off-white powder
Source: Semi-synthesized with 10-DAB
Type: APIs
The History of Hande GMP
1. In 1996, the quality system was established and obtained DMF.
2. In 2004, FDA on-site inspection obtained CGMP certificate.
3. In 2009, semi-synthetic paclitaxel DMF and natural paclitaxel CEP were obtained.
4. In 2011, semi-synthetic paclitaxel CEP was obtained.
5. In 2012, passed the TGA on-site inspection, obtained GMP certification, and passed the FDA on-site inspection.
6. In 2013, passed the CGMP site.
7. In 2015, India was registered and Japan was registered.
Hande production capacity
Production cycle: 30-45 days.
Production batch: one batch can produce about 15kg.
Hande production capacity: there is inventory and can be mass produced.
Hande Strength
Hande Company has a research and development team for many years. The team has applied for a number of patented inventions and achieved seamless process connection from laboratory to commercial mass production. The self built GMP production base has successively passed the regulatory review of the US FDA, EU EDQM, China GMP, Japan PMDA, Australia TGA, South Korea, India, Taiwan, China, Türkiye, Russia, SGS, Dun&Bradstreet, etc. At the same time, the company is equipped with a research and development team and has successively obtained a number of patents. QC testing room, highly realizing product project testing.
Our Services
1.Products:Provide high-quality,high-purity plant extracts,pharmaceutical raw materials,and pharmaceutical intermediates.
2.Technical services:Customized extracts with special specifications according to customer requirements.
Be the best supplier of raw materials and enterprises with integrity!
Welcome to contact me by sending email to marketing@handebio.com