-
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)