Personal Information
Organization / Workplace
Greater Boston Area United States
Occupation
Graduate Student at Northeastern University,Regulatory Affairs in Drugs & Medical Devices, Seeking for Full-time positio
Industry
Medical / Health Care / Pharmaceuticals
About
More than two years of working experience in Regulatory Affairs for drugs and medical devices. Experienced in documentation, assistance in troubleshooting market complaints and audits for various markets ( US, Canada, EU, Brazil, etc.) for both drugs and medical devices, and compilation of technical dossier (for devices) or drug master file (DMF).
Skills: Regulatory submissions and documentation, QMS, cGMP and CMC compliance, change controls and quality management systems, new product development, clinical research, IND, NDA, ANDA, IDE, 510(k), PMA, IVD, MDD (Medical device Directives), CAPs (conformity assessment procedures), BLA, EU filing, other international filing and registrations,...
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business model
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(1)Personal Information
Organization / Workplace
Greater Boston Area United States
Occupation
Graduate Student at Northeastern University,Regulatory Affairs in Drugs & Medical Devices, Seeking for Full-time positio
Industry
Medical / Health Care / Pharmaceuticals
About
More than two years of working experience in Regulatory Affairs for drugs and medical devices. Experienced in documentation, assistance in troubleshooting market complaints and audits for various markets ( US, Canada, EU, Brazil, etc.) for both drugs and medical devices, and compilation of technical dossier (for devices) or drug master file (DMF).
Skills: Regulatory submissions and documentation, QMS, cGMP and CMC compliance, change controls and quality management systems, new product development, clinical research, IND, NDA, ANDA, IDE, 510(k), PMA, IVD, MDD (Medical device Directives), CAPs (conformity assessment procedures), BLA, EU filing, other international filing and registrations,...
Tags
business model
See more