Good Laboratory Practice


SNBL Japan is committed to the principles of Good Laboratory Practice and are able to conduct preclinical studies in compliance with US FDA GLP, OECD GLP, as well as our standard Japanese PMDA GLP, and other types of GLP. Our Drug Safety Laboratories and Pharmacokinetics and Bioanalysis Center are both GLP facilities. The Japanese Ministry of Health, Labour, and Welfare inspects our facilities every 3 years and we have received the highest grade available on every certificate issued since 1985.

Please contact us to discuss how we can meet your GLP study needs.

 

Japanese Pharmaceutical GLPA-level evaluation since 1985, Approved since 2016

Inspection period

Result

Pass date

2015-12-07 to 2015-12-11

Approved

2016-02-05

Japanese Medical Device GLPA-level evaluation since 2007, Approved since 2016  

Inspection period

Result

Pass date

2015-12-07 to 2015-12-11

Approved

2016-02-05

Japanese Regenerative Medicine GLPApproved since 2016  

Inspection period

Result

Pass date

2015-12-07 to 2015-12-11

Approved

2016-02-05

Japanese Chemical Substance GLPApproved since 1990

Period

Result

Pass date

Application for Confirmation of Compliance with the Chemical Substances Control Law  (2016)

Approved

2016-06-02