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Afsaneh Motamed Khorasani

Dr. Motamed Khorasani is keynote speaker at Compliance Key and She is a Medical Affairs expert and a Senior Scientist with a strong background in biomedical science and clinical trials. 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, Medtronic (Covidien), 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.

Education:
2008 - Post-Doctoral Fellowship, Microbix Biosystems Inc., Mississauga, Canada
2006 - PhD, Molecular Biology/Cancer informatics, University of Toronto, Canada
1999 - MSc, Molecular Biology/Infertility/In vitro Fertilization, University of British Columbia, Canada
1992 - BSC, Medicine (Obstetrics), University of Shahid Beheshti, Iran

Area of expertise:
Medical Affairs
Regulatory affairs
Clinical Trials (design & execution)
Regulatory Writing/Submission (global)
Therapeutic areas (Molecular Biology, Biology, Biochemistry, Bioinformatics, Oncology, Hematology, Atherosclerosis, Blood, Immunology, Infectious Disease, Neuroscience, Nutrition, Bone metabolism, Rheumatology, Skin, Diabetes and Metabolic Disorders, Endocrinology, Pharmacology, Physiology, and rare diseases)

 Webinar Id: LSHCAM002
10:00 AM PT | 01:00 PM ET
 11/14/2018
 Duration 60 mins

Good Documentation Guideline (Chapter <1029> USP)

Good Documentation Practices (GDP) is a critical and essential part of a regulated environment (pharmaceutical and medical device manufacturing, R&D, laboratories and clinical trials). Compliance with GDP ensures an auditable account of work. It ensures integrity and control of documents and is a key requirement for a developed quality system. This training session will cover the US Pharmacopeia General Chapter <1029> and all aspects of........


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                $179
       Single Attendee
(Only for one Participant)
          $368
Multiple Attendee
( 2 - 5 Participants)
          $741
Corporate Attendee
( 6 - 10 Participants)
                   $167
         Recorded
(6 months unlimited access)



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