Ming Ji
MingJi,SeniorMedicalDirector,ClinicalSafetyEvaluateatABBOTTLABORATORIES.MDwithover18yearspharmaceuticalindustryexperienceinnewdrugdevelopmentandsafety.Overseeingdrugsafetyandpharmacovigillanceorganizationsandactivities,IND/NDA/BLAsubmissions,regulatoryagencyinteractions(FDA,EMEAandothers),developmentofglobalstrategiesforsmallmoleculesandbiologicals,phase1-4clinicaltrials,benefit/riskassessment,newdrugsafetyprofiling,riskmanagement,safetysignaldetection,workedonpartnershipswithmultiplecompanies.Extensivemanagementexperience.
Ming Ji,Senior Medical Director, Clinical Safety Evaluate at ABBOTT LABORATORIES.MD with over 18 years pharmaceutical industry experience in new drug development and safety. Overseeing drug safety and pharmacovigillance organizations and activities, IND/NDA/BLA submissions, regulatory agency interactions (FDA, EMEA and others), development of global strategies for small molecules and biologicals, phase 1-4 clinical trials, benefit/risk assessment, new drug safety profiling, risk management, safety signal detection, worked on partnerships with multiple companies. Extensive management experience.
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Ming Ji
Ming Ji  MingJi,SeniorMedicalDirector,ClinicalSafetyEvaluateatABBOTTLABORATORIES.MDwithover18yearspharmaceuticalindustryexperienceinnewdrugdevelopmentandsafety.Overseeingdrugsafetyandpharmacovigillanceorganizationsandactivities,IND/NDA/BLAsubmissions,regulatoryagencyinteractions(FDA,EMEAandothers),developmentofglobalstrategiesforsmallmoleculesandbiologicals,phase1-4clinicaltrials,benefit/riskassessment,newdrugsafetyprofiling,riskmanagement,safetysignaldetection,workedonpartnershipswithmultiplecompanies.Extensivemanagementexperience.
MingJi,SeniorMedicalDirector,ClinicalSafetyEvaluateatABBOTTLABORATORIES.MDwithover18yearspharmaceuticalindustryexperienceinnewdrugdevelopmentandsafety.Overseeingdrugsafetyandpharmacovigillanceorganiza...
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Ming Ji,Senior Medical Director, Clinical Safety Evaluate at ABBOTT LABORATORIES.MD with over 18 years pharmaceutical industry experience in new drug development and safety. Overseeing drug safety and pharmacovigillance organizations and activities, IND/NDA/BLA submissions, regulatory agency interactions (FDA, EMEA and others), development of global strategies for small molecules and biologicals, phase 1-4 clinical trials, benefit/risk assessment, new drug safety profiling, risk management, safety signal detection, worked on partnerships with multiple companies. Extensive management experience.

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