• In 1954
    In order to meet the new demanding of drugs package in Taiwan, “East Chemical Co.” started to develop the technique of manufacturing the Empty Hard Gelatin Capsules.
  • In 1971
    Established SHING YUANG FONG Enterprise Co., Ltd.
  • In 1977
    Manufacturing capacity expansion. Factory facility moved to Wu Feng District, Taichung City.
    Additional company “SHING LIH FANG Enterprise Co., Ltd.” was set up.
    Meanwhile, beginning with 100% automatic production.
  • In 1987
    The plant structure was improved to comply with GMP Status. Shing Lih Fang was the first capsule manufacturer who obtained it in Taiwan.
  • In 1999
    Obtained ISO 9001 Certification. (And continuously achieved the most updated qualification).
  • In 2000
    We obtained the HALAL Certificate.
  • In 2003
    We finished and achieved the full steps of cGMP standard.
  • In 2006
    We purchased two “Capsules Appearance Inspection Machines” from Japan.
  • In 2007
    Certification approved in Drug Mater File granted by the U.S. Food and Drug Administration. (DMF NO.: 20588)
    We had been audited by Wyeth Global Compliance Auditing Group, and obtained the qualified supplier qualifications. (“Wyeth” is belong to the“Pfizer Pharmaceutical Co.” now)
  • In 2011
    Now, we are lasting to achieve the new regulation standard, which is defined by our authority TFDA (Taiwan Food and Drug Administration).
  • In 2012
    We had been audited by Pfizer Global Compliance Auditing Group, and obtained the qualified supplier qualifications.
  • In 2013
    Importing two sets of Capsule Appearance Inspection Machine from France.
  • In 2015
    Importing three sets of Capsule Appearance Inspection Machine from China.
  • In 2015
    We obtained the PIC/S GMP-Certificate.
  • In 2018
    We continuously audited by Pfizer Global Compliance Auditing Group, and keep the qualified supplier qualifications.
  • In 2019
    We obtained the PIC/S GDP-Certificate.
  • In 2020
    Certification approved in Drug Mater File granted by National Medical Products Administration. (NMPA NO.20180001281)