April20-21,2017Day one morning-Global Industry trends
Day one afternoon to Day two
Stream A -Drug Substance
Stream B --Formulation Design and development
Stream C-- Analytical Development and Support
Stream D-- Regulatory Planning and BE Studies Session
The company has been engaged in GLP research of drugsince 2005, achieved a full set of GLP qualification of CFDA, and hassuccessfully passed the international AAALAC accreditation as well as mutualexam of toxicology lab with US EPA. The company has been devoted into supplyingdrug non-clinical evaluation complying with international standard includingpharmacodynamics, pharmacokinetics and drug safety evaluation professionally.