GMP consultancy and execution services
Company provides specialized technical and regulatory services... 
Drug registration support service
Provide registration service of target market as required by ...
Audit services
Audit services include compliance audit, supplier audit and ....
Foshan RuiTong Consulting Co.,Ltd. is a specialized technical services company for providing services on drug GMP... >>MORE
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Congratulate Henan Topfond Sci-Tech Co.,Ltd. on passing US FDA on-site inspection in November, 2024
Foshan RuiTong Consulting Co.,Ltd. (afterwar…
Warmly congratulate Henan Topfond Sci-Tech Co., Ltd. on passing the FDA on-site inspection with “zero” deficiency and obtaining the EIR issued by FDA!
Foshan RuiTong Consulting Co., Ltd. (afterwa…
TOP TEN DEFICIENCIES IN NEW APPLICATIONS FOR CERTIFICATES OF SUITABILITY FOR CHEMICAL PURITY
This document is a summary of the top te…
Warmly congratulate Anhui Xingzhou Pharma Co.,Ltd. on obtaining drug manufacturing license
Foshan RuiTong Consulting Co.,Ltd. (afterwar…
Warmly congratulate Henan Topfond Sci-Tech Co.,Ltd. on passing US FDA on-site inspection with zero deficiency
Foshan RuiTong Consulting Co.,Ltd. (afterwar…
Review of Drug Project for One US Company
US company Shaanxi Co.,Ltd.（afterwards abbre…
Summary of Correction for FDA483 and DMF Deficiencies of Luohe Nanjiecun Pharmaceutical Group Pharmacy Co., Ltd.
Luohe Nanjiecun Pharmaceutical Group Pha…
Status Update of European and American Certification Project of Luohe Chief Pharmaceutical Co.,Ltd.
Luohe Chief Pharmaceutical Co., Ltd. (afterw…
Review and Prospect on European and American Certification Project of Luohe Chief Pharmaceutical Co., Ltd.
Luohe Chief Pharmaceutical Co., Ltd. (af…
Congratulations to Hubei Nokete Pharmaceutical Co.,Ltd. for obtaining CEP granted by EDQM
Hubei Nokete Pharmaceutical Co.,Ltd., lo…
Typical Mistake & Deficiencies During Construction of New Pharmaceutical Facilities
Foshan RuiTong Consulting Co.,Ltd. (Abbrevia…
Submitting DMF using electronic common technical documents (eCTD)
Since May 5, 2018, Master files must be submi…
2017 Drug Inspection Report Issued by CFDA
CFDA已于2018年06月08日颁发了《2017年度药品检查报告》。 《2017年…
Top Ten deficiencies – New Applications for Certificates of Suitability for chemical purity(2015-2016)
EDQM has published the document 《Top ten def…
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