Back to Results
First PageMeta Content
Pharmacology / Food safety / Pharmaceuticals policy / Good Laboratory Practice / Organisation for Economic Co-operation and Development / Good manufacturing practice / Verification and validation / Clinical trial / Food and Drug Administration / Pharmaceutical industry / Pharmaceutical sciences / Health


Questions and Answers (Guidance Document Non-Clinical Laboratory Study Data Supporting Drug Product Applications and Submissions: Adherence to Good Laboratory Practice)
Add to Reading List

Document Date: 2013-06-24 11:49:35


Open Document

File Size: 58,08 KB

Share Result on Facebook

Company

GLP Working Group / Will Health Canada / /

Country

Germany / United States / Netherlands / Canada / United Kingdom / /

Facility

Good laboratory Practice / /

IndustryTerm

facility/site / pharmaceuticals / outside monograph applications / exempt nonprescription products / pest control products / drug product / recognition audit / nonprescription products / requirements products / natural health products / combination products / food additives / /

Organization

Health Products and Food Branch / Advisory Council on Conformity Assessment / Organisation for Economic Co-operation and Development / Canadian Monitoring Authority / Pest Management Regulatory Agency / SCC’s GLP monitoring authority / Standards Council of Canada / Canadian Government Agency / European Commission / Monitoring Authority / Bureau of Policy / Science and International Programs / Medicines and Healthcare products Regulatory Agency / office of the Auditor General / GLP Monitoring Authority / United States Food and Drug Administration / /

Position

principal investigator in the United Kingdom / study director / /

Technology

radiopharmaceuticals / /

SocialTag