ComplianceOnline

Expert Profile


Dr. Afsaneh Motamed Khorasani
Vice President of Medical Affairs, Easy Global Training

Dr. Afsaneh Motamed Khorasani, PhD, is a Medical and scientific Affairs expert and a Senior Scientist with a strong background in biomedical science and clinical trial/research. She has a tenured and diverse range of experience in medical affairs, basic and industrial clinical research and development, clinical trials, Medical and regulatory writing and intellectual property. She is currently the Vice President of Medical Affairs at Easy Global Training, which is a US-based firm providing global regulatory, quality and medical affairs training backed by consulting. Before joining this company, Dr. Motamed Khorasani has served as an independent consultant, director of medical affairs, senior medical sciences liaison, senior scientist and senior medical analyst at Merck (MDS), Johnson & Johnson, United States Pharmacopeia Convention (USP), Amgen, Baxter International, Covidien (eV3), Radient Pharmaceuticals, AMDL Diagnostics, Microbix Biosystems, Neometrix Consulting, Mount Sinai Hospital, Princess Margaret Hospital, and Vancouver General Hospital.

She has more than 20 years of experience and many National and international certificates in GLP, GMP, ICH-GCP and global regulatory compliance for clinical trials and is a member in a number of professional associations, including: American Association of Cancer Research (AACR), American Medical Writers Association (AMWA), Regulatory Affairs Professional Society (RAPS), American Society of Quality (ASQ), Project Management Institute (PMI), and Intellectual Property Institute of Canada (IPIC). Dr. Motamed Khorasani's research has focused on high throughput approaches in the context of cancer informatics with a particular interest in the use of comparative analysis for the mining of integrated oncology datasets that include protein-protein interaction and gene expression profiling. She has published and presented more than 50 papers, abstracts and articles in highly regarded scientific journals and high profile conferences and scientific meetings.

Trainings by Expert

Good Documentation Guideline (Chapter <1029> USP)
Category: Drugs and Chemicals (Pharma) , Medical Devices , Clinical Research , Biotechnology , Laboratory Compliance , All FDA Regulated Industry , FDA Audit and Inspection , GXP Pharmaceutical , GXP Medical Devices , Documentation and IT , Quality and Safety , Audits & Inspections , QMS, ISO 13485, CAPA , Laboratory , Quality & Safety , Food & Dietary Supplements , Manufacturing & Contamination control , Drugs Regulations , Clinical Trial Regulations , Biotech Regulations , Audit & Inspection-Role , All FDA Reg. based Audit , Food Safety & Quality , Life sciences QA/QC , Research & Development , Drug R & D , Device R & D , Regulations & Guidances , Life Sciences , Regulatory Affairs , Common FDA Regulations , QA/QC

How to Prepare a Standard Operating Procedure (SOP)?
Category: Drugs and Chemicals (Pharma) , Medical Devices , Clinical Research , Biotechnology , Laboratory Compliance , Risk Management , Packaging and Labeling , All FDA Regulated Industry , Food Safety Compliance , FDA Audit and Inspection , FDA Validation , Testing and Validation , Documentation and IT , Quality and Safety , Audits & Inspections , Sterilization , Supply Chain and Manufacturing , R & D , Laboratory , GLP & Other Best practices , Microbiology Laboratory , Clinical Laboratory , Analytical Laboratory , Drug Development , GCP & Other Best Practices , Trial Design and Management , Quality & Safety , Food & Dietary Supplements , Storage and Distribution , Manufacturing & Contamination control , Drugs Regulations , Clinical Trial Regulations , Biotech Regulations , Audit & Inspection-Role , Quality Audit , Food Safety Audit , All FDA Reg. based Audit , Medical Device Inspection , Lab Audit , Drugs Inspections , Clinical Research Audit , Documentation and Policy Management , Lifescience process & Procedures , Food Safety & Quality , Life sciences QA/QC , Research & Development , Drug R & D , Device R & D , Regulations & Guidances , Life Sciences , Regulatory Affairs , Documentation and Data Management , Common FDA Regulations , ISO 22000 , HACCP , QA/QC

Good Documentation Practice and Record Keeping Regulations (FDA & EMA)
Category: All FDA Regulated Industry , Documentation and Policy Management , Life Sciences , Regulatory Affairs , QA/QC

Coronavirus and a New Member of This Family (COVID-19) - What You Need to Know
Category: All FDA Regulated Industry

Pack of 3 Trending Courses on USP Standards
Category: Drugs and Chemicals (Pharma)