Pr. Peivand Pirouzi, Ph.D. in Physiology and Biophysics, MBA, CCPE, Tenured Professor, Seneca College of Applied Arts and Sciences, a Polytechnique institute in Canada
Tenured Professor, Academic Program Coordinator, and Clinical Research Director, teaching at the Faculty of Applied Arts and Health Sciences at Seneca. Professor and consultant, Canadian Food and Drugs Act and International Guidelines (GCP, GMP, GVP) related to Medical Research, Pharmaceutical Sciences and Product Registration, inspections and audits including Prescription drugs, Medical devices, Natural Health Products, Cosmetics, Food and Medical Marihuana. Twenty eight (28) years of experience in Academic teaching and Curriculum development, Medical and Pharmaceutical Research, Corporate Training, Career development and supervised training and consulting in France and Canada. Corporate consultant offering continuing education programs to Governmental Agencies, Universities, Colleges, Pharmaceutical Companies in Health Sciences fields including Medicine, Nursing, Occupational Health and Safety, Mental Health, Addiction, Clinical Research, Drug Safety and Pharmacovigilance, Regulatory Affairs, Quality Assurance, Medical Marijuana Regulations, Audits and Regulatory Inspections, Good Pharmaceutical Industry Practices (GxPs) and various International laws, regulations and guidelines.
Pr. Guita Akbari Azad, D.V.M., Ph.D., Post Graduate College certificate in Regulatory Affairs and Submission Management
To be posted soon!
Pr. Saeed Karamzadeh, Ph.D. in Plant Ecophysiology, Post Graduate College certificate in ACMPR
R&D director of Ruyesh Agro Company, Science&Technology Park, Tehran University, More than 15 years of experience as a research scientist in: Agronomy, Crop Environmental Stresses, Plant Tissue culture, Domestication and adaptation of Medicinal plants, More than 10 years of experience in teaching: Crop physiology, Crop production, Medicinal plants, Official Inspector, Adviser, and Certification of Hybrid Corn Seed production in national scale, PhD in Plant Eco-physiology (UCD,Ireland), MSc in Agronomy, and a College Post Graduate Certificate in ACMPR from the Crown Medical Research and Pharmaceutical Sciences College of Canada.
Dr. Ati Safarii, M.D., Post Graduate College certificate in Pharmacovigilance and Drug Safety
M.D., with a Post Graduate College Certificate in Pharmacovigilance and Drug Safety from the Crown Medical Research and Pharmaceutical Sciences College of Canada with medical and educational experience in multinational pharmaceutical companies, Healthcare Organizations and medical research college, Ati has outstanding experience in developing medical affairs and marketing strategies merged with in depth understanding of business opportunities and analysis of the market and return on investment. She is skillful in medical training, scientific presentation and educational event planning including CMEs and KOL relationship management and has advanced scientific expertise in different disease areas i.e. like Neurology and Psychiatry.
Dr. Sanaz Manteghi, M.Sc., Ph.D. Biochemistry, Post Graduate College certificate in Regulatory Affairs
Dr. Manteghi is a researcher and a Biochemist with ten years of professional experience in teaching and mentoring undergraduate and graduate students, as well as laboratory technicians in academic and clinical laboratory settings. Sanaz holds a Ph.D. in Biochemistry from department of biochemistry, McGill University, Montreal, Canada, and a post graduate certificate in Pharmaceutical Regulatory Affairs and Submissions from Crown Medical Research and Pharmaceutical Sciences College of Canada, Toronto, Canada. She obtained her M.Sc. in Cell and Molecular Biology and her B.Sc. in Biology from Iran. She has extensive experience in planning, coordinating and executing pre-clinical and clinical projects, conducting literature review, developing assays, preparing manuscripts, grant applications, and monitoring study compliance. In addition, she received several awards and successfully published several articles in peer reviewed journal. Sanaz has the experience in generating and reviewing variety of regulatory documents, reports, forms and applications such as NDS, SOPs, product Monographs, and QA/ QC reports based on regulatory guidelines and requirements.
Dr. Amani Salama, M.D., Post Graduate College certificate in Clinical Research, Pharmacovigilance, Quality Assurance and ICH-GMP
Dr. Amanai is a fully bilingual (English/French) medical practitioner and research scientist with eight years of experience in Pharmacovigilance and Drug Safety fields, performed pharmacoepidemiological surveys, implemented and maintained effective organisational systems of medical records, charts and insurance claims, is experienced in processing, evaluating, and conducting medical review and submitting all the Safety reports for the clinical and post-marketing phases, performed quality assurance audits of clinical trials in compliance with Good Clinical Practice (ICH-GCP), Standard Operating Procedures (SOPs), study protocols and regulations from FDA and Health Canada
Dr. Amirmasoud Nikahd, M.D., Post Graduate College certificate in Clinical Research and Pharmacovigilance
MD, Clinical Research Assistant at Sunnybrook Health Sciences Centre, Advisory Committee Member at DENACRC Inc., with over 14 years of experience working in clinical environment with strong understanding of Clinical Research processes according to Study Protocols, ICH/GCP, Guidelines and Health Authority requirements. He has the experience to develop and implement a Clinical Research Study, plan, manage and develop effective communication strategies including IRB and Ethics Board communication. He has practical knowledge of project management tools and techniques to accurately determine key study parameters and to estimate time, cost (Budgeting) and resource allocation in Clinical Trials. Amirmasoud has research experience in Data Collection, Data Entry and Analysis, knowledge of Study Protocols, preparing Informed Consent Forms ( ICF) and Investigational Brochures ( IB ), is familiar with Clinical Research Inspections and writing site visit audit report, and experience in recruiting and screening participant subjects in clinical research studies
Alex Ghasemi, M.Sc. in Chemistry, Post Graduate College certificate in Quality Assurance and regulatory Affairs
Alex is a consultant with working experience related to Canadian Food and Drugs Act and International Guidelines (GCP, GMP, GVP) related to Medical Research, Pharmaceutical Sciences and Product Registration, inspections and audits including Prescription drugs, Medical devices, Natural Health Products, Cosmetics, Food and Medical Marihuana.
He is a quality professional with over 7 years of progressive experience in the food and pharmaceutical industry and has thorough knowledge and experience in quality compliance, regulatory ,development, submissions,validation,Quality Systems, Deviation, Investigations and auditing. Ali has extensive experience in QC laboratory testing product using validated methods and techniques such as HPLC, Dissolution , NMR, UV, FTIR, NIR, Karl Fischer, Particle Size and Wet Chemistry
Lida MoradKhani, M.Sc. in Chemistry, Post Graduate College certificate in Clinical Research (Humber) , QA and Regulatory Affairs (Crown)
Lida has the following skills and experience in several pharmaceutical fields:
-Working Knowledge and experience in cGMP, GLP, GDP, FDA,HFPB regulations, ICH and GCP guidelines, TCPS, SOP, Protocol, CRF,ICF,medical terminology
- Strong Knowledge in bio-availability, Project management in clinical trial, Pharmacology( PK/PD), Medical devices
- Highly organized and strong management skills, commitment to maintaining quality and efficiency
- Data entry and checked the errors to prepare accurate data
- Audited the confidential documents
- familiarity with preparing REB document
-Reviewed patient 's medical report and medical chart
-Reviewed literature , extracted key words , analyzed data , and prepared a brief summary
- Excellent critical thinking and problem solving skills
-self- directed in all aspect of the study project
Forouzandeh Haghollahi, M.Sc. in Analytical Chemistry, Post Graduate College certificate in Clinical Research (Humber) , QA and Regulatory Affairs (Crown)
Forouzandeh has over six years of experience as a Quality Control and Assurance Associate with extensive knowledge on HPLC, FTIR, GMP, UV-VIS, KF, GLP, GC, SOP and WET CHEMISTRY. She has solid knowledge and understanding of principles around dealing with measures, testing, inspections, verification and auditing based on Health Canada and FDA regulations with working knowledge of Health and Safety practices. She has a Master degree in Analytical Chemistry, studies in advanced HPLC program at Seneca College. She hols a College post graduate certificate in Quality assurance and ICH-GMP from the Crown Medical Research and Pharmaceutical Sciences College of Canada where she is acting as a GMP consultant for the review of technichal and audit reports, writing administrative and operational SOPs, working instructions, and analytical methods, and developping validation methods and audit checklists in the fields of Pharmaceuticals, Natural Health Products, and Cannabis Industry in Canada.