CN / EN

Huayi Pharmaceuticals (Anhui) Co., Ltd.is the first company passing European certification in Anhui. As a contract development and manufacturing organization (CDMO) dedicated to providing various dosage forms for Chinese and European markets, the company has been granted with EU GMP certificate in August 2010 after passing the GMP inspection by Medicines and Healthcare Products Regulatory Agency (MHRA). The certificate has been updated three times after re-inspections by MHRA. The company also has passed the quality inspections by more than 200 companies at home and abroad including Teva, KrKa and Novartis etc. and has passed several GMP compliance inspections by Chinese authorities (NMPA).


Since its establishment, the company has been providing joint venture cooperation, multiple dosage forms pharmaceutical development, commercial production on a contract basis, chemical synthesis research, and drug clinical testing services for research institutions and pharmaceutical sales enterprises etc. at home and abroad and has gradually built an open CDMO platform for international markets, which is dedicated in R&D of multiple dosage forms and focused on manufacturing of oral preparations, providing chemical synthesis as supplementary service.

Adhering to the corporate value of “create value and benefit for the world” and corporate spirit of “keep pragmatic and innovative all the time”, Huayi is fully engaged in providing customers with pharmaceutical development and production services of high efficiency, high quality and controllable cost and making high quality drugs at affordable cost. Huayi sincerely looks forward to cooperating with partners from all over the world on the pharmaceutical development, contract manufacture, MA application in both China and Europe and joint venture cooperation and developing both the international and domestic markets.


  • 3 billion

    tablets/capsules manufactured per year on a contract basis

  • 300 ?

    products successfully developed and commercialized

  • 200 ?

    quality audits from well-known pharmaceutical companies at home and abroad

Milestone

  • 2024

    ? Passed the fifth EU inspection in November 2024

    ? Synthesis laboratory constructed

    ? Phase I Preparation Building in the New Site
      (Shenyang Road Site) Put Into Use 

    ? High potent solid preparation workshop under 
      construction


  • 2023

    ? The Fourth Council Member Unit of the All-China
       Federation of Industry and Commerce Association
       of Pharmaceutical Commerce

    ? Top 20 Chinese Pharmaceutical CDMO Enterprises
       in 2023

    ? Main Structure Construction for Phase I Preparation
       Building in the New Site (Shenyang Road Site)
       completed

    ? Construction of synthesis laboratory started

    ? Construction of highly potent solid preparation
       workshop started

    ? Exports to EU reached 2.5 billion tablets

    ? First domestic product commercialized

  • 2022

    ? On September 13, 2022, the company was elected
       as the Chairman Unit of Anhui Preparation CDMO
       Industry Alliance

    ? Top 20 Chinese Pharmaceutical CDMO Enterprises
       in 2022

    ? 2022 (Industry) Leading Enterprise

  • 2021

    ? On October 8, 2021, Huayi’s Technical Center was
       established.

    ? In June 2021, the company passed the remote
       re-inspection by MHRA.


  • 2020

    ? On July 14, 2020, Huayi produced the first bottle of
       oral liquids preparation with the Oral Liquid
       Preparation Workshop put into operation.

  • 2019

    In 2019, we were named as one of the Top 50 Growing
      Enterprise of the Chinese Pharmaceutical Industry.


  • 2018

    In 2018, contract manufacturing output reached
       1.6 billion units and we began construction of our
       oral liquid preparation workshop and high-potency
       workshop.


  • 2016

    ? In 2016, the company passed re-inspection by MHRA
       without any major deficiencies. The workshop
       extension passed MHRA certification and the
       company’s annual capacity was increased to 3 billion
       units.


  • 2012

    In 2012, the company passed re-inspection by MHRA.


  • 2010

    ? In 2010, we passed the on-site inspection by MHRA and
       received EU GMP certification. We became the 12th
       solid dose pharmaceutical plant to pass EU GMP
       accreditation in China. We started manufacture for the
       EU market.


  • 2006

    ? In 2006, Huayi Pharmaceutical (Anhui) Co., Ltd., a
       Sino-British joint venture, was established. Land
       was purchased and the factory designed.