中文
NAME

To be the most Reliable Supplier in the Global
Pharmaceutical Supply Chain

NAME

To be the most Reliable Supplier in the Global
Pharmaceutical Supply Chain

About Us ABOUT ENTERPRISES
Corporate Profile

Chongqing Sintaho Pharmaceutical Co., Ltd., founded in 2016, is a high-tech and international enterprise focusing on API R&D and manufacturing, located in Chongqing International Biological City and covering an area of 83 acres. Its holding company - Chongqing Taihao Pharmaceutical Co., Ltd., has been inspected successfully by National Medical Products Administration (NMPA), U.S. Food and Drug Administration (FDA), European Directorate for Quality Medicines (EDQM), Pharmaceuticals and Medical Devices Agency (PMDA) and etc.

Sintaho has built high standard production lines for highly active and toxic APIs in accordance with the international and domestic cGMPs, with a professional EHS and cGMP team covering R&D, production, quality management and regulatory registration, which comprehensively upgrades the management system in accordance with the cGMP regulations, ICH guidelines and EHS management standards, based on years of experience. Sintaho has been committed to building a high-end CDMO platform for oncology APIs with industry influence to produce high quality pharmaceuticals to improve human health.

Corporate Profile
Our Journey to Excellence
  • 2023

    Obtained Paclitaxel CEP Certificate

  • 2022

    Passed the Australian TGA Remote GMP Inspection

  • 2021

    Launched the 1st Product

  • 2018

    Successfully Passed the 4th USFDA On-site Inspection

  • 2017

    Successfully Passed France ANSM On-site Inspection and the GMP Certificate Granted Accordingly

  • 2016

    Sintaho Established

  • 2015

    Successfully Passed the 3rd USFDA On-site Inspection and CEP Certificate for Docetaxel Trihydrate Granted

  • 2014

    Successfully Passed the 2nd Japan PMDA On-site Inspection

  • 2013

    CEP Certificate for Docetaxel Granted

  • 2012

    Successfully Passed the 2nd USFDA On-site Inspection and CEP Certificates for Oxaliplatin and Paclitaxel (Natural) Granted

  • 2010

    Successfully Passed the 1st Japan PMDA On-site Inspection

  • 2008

    Successfully Passed the 1st USFDA On-site Inspection

  • 2004

    Taihao Established