GLP Consulting & Training

NSF Pharmalytica offers expert consultation and study monitoring for toxicology and pharmacokinetic studies. NSF Pharmalytica also functions as a third-party CRO, interacting directly with your toxicology CRO for analytical testing. Confidentiality agreements between NSF Pharmalytica and the major toxicology CROs allows for direct communication of our staff with the study directors at the CROs. This ensures that any issues are communicated to the study director in a timely manner and also allows NSF Pharmalytica to submit our entire QA file for review to the study director at your CRO.

Study monitoring is performed on a consultancy contract basis. GLP studies are routinely monitored for formulation, analytical chemistry, dosing, TK/PK, clinical observations, necropsy, report and data review. Written status reports are provided to the client on a monthly basis or more frequently, upon request.

In addition, we offer in-company GLP training courses. Please contact us today to set up a course that is tailored to your specific needs.