3 months agoRegulatory Affairs - Applications of QSR for Medical Devices: 21 CFR Part 820 and ISO 13485 by Peivand Pirouzi, Ph.D.Application of Quality System Regulation in Medical Device Design & Manufacturing
4 years agoOpen College with Dr. Stephen Hicks | EP #48 | Schooling to Develop or Stunt Kids’ Potential?Open College Podcast with Dr. Stephen Hicks
4 years agoOpen College with Dr. Stephen R.C. Hicks | EP#1 | Free Speech; Why The Philosophy MattersOpen College Podcast with Dr. Stephen Hicks
3 months agoClinical Research - Scientific Assessment and Data Analysis - Statistical concepts for clinical studies in pharmaceutical and Health care research. P.Pirouzi,Ph.D.CrownCollege
3 months agoClinical Research - Interpretation of clinical and non clinical data in pharmaceutical and health care research. Peivand Pirouzi, Ph.D.CrownCollege
3 months agoClinical Research - Artificial Intelligence and Statistical Analysis of Clinical trial data in R Studio (Health Care Research). P.Pirouzi, Ph.D.CrownCollege
3 months agoRegulatory Affairs - Completion of Health Canada form PSEAT for CTA application. Peivand Pirouzi, Ph.D.CrownCollege
3 months agoData Science and Data Management - Careers in Research Analysis field-Skills and training required for job applicants. P.Pirouzi, Ph.D.CrownCollege
3 months agoRegulatory Affairs - EMA - Marketing Authorization Applications for Pharmaceutical Products in EU. Peivand Pirouzi, Ph.D.CrownCollege
3 months agoCareer Management - Prepare for Careers in Pharma, Food, Medical Devices, NHPs, Cosmetics & Medical Cannabis in Canada. Peivand Pirouzi, Ph.D.CrownCollege
3 months agoRegulatory Affairs - FDA databases: Drugs@FDA and Clinical trials.gov - Live demonstrations - Peivand Pirouzi, Ph.D.CrownCollege
3 months agoRegulatory Affairs - Clinical Trials Information System in Europe (EMA-Clinical Research). Peivand Pirouzi, Ph.D.CrownCollege
3 months agoRegulatory Affairs - Health Canada Form-0292-Medical Devices Establishment Licensing (MDEL) Application. P.Pirouzi, Ph.D.CrownCollege
3 months agoRegulatory Affairs and Quality Assurance - US Current Good Manufacturing Practices (cGMP) and CMC for pharmaceutical products. Peivand Pirouzi, Ph.D.Fundamentals of CMC Regulations and Methods for Pharmaceuticals
3 months agoRegulatory Affairs - eCTD Submission Gateways for FDA and EMA, and ICH-M8 (Pharmaceutical Sciences and Health Care products). Peivand Pirouzi, Ph.D.Global Impact of (eCTD) Submissions
3 months agoEpidemiology and Public Health - Summarizing Data in Epidemiology for Health care research managers. Peivand Pirouzi, Ph.D.Fundamentals of Epidemiology for Health Service Managers
3 months agoRegulatory Affairs - Introduction to Pharmaceutical Quality, CMC, ICH-M4 eCTD Module 2 and 3 for drug registration. Peivand Pirouzi, Ph.D.Fundamentals of CMC Regulations and Methods for Pharmaceuticals
3 months agoPharmaceutical Clinical Research Careers-Required Skills and Qualifications. Peivand Pirouzi,Ph.D.CrownCollege
3 months agoRegulatory Affairs - Health Canada-Preparation of Meeting Application Packages for CTA,NDS,SNDS. Peivand Pirouzi, Ph.D.CrownCollege
3 months agoRegulatory Affairs Project Management: NDS in CTD Format for Health Canada by Peivand Pirouzi, Ph.D.CrownCollege
3 months agoRegulatory Affairs - Global Regulatory Harmonization for drugs & medical devices- IMDRF and ICMRA. Peivand Pirouzi, Ph.D.CrownCollege
3 months agoRegulatory Affairs and eCTD - Pharmaceutical and health care research. Peivand Pirouzi, Ph.D.Global Impact of (eCTD) Submissions
3 months agoFDA Registration: Dietary Supplements, Conventional Foods, and NDIs by Peivand Pirouzi, Ph.D.CrownCollege
3 months agoRegulatory Affairs and Quality Assurance - Pharmaceutical Inspections and Audits (Based on ICH-Q10). Peivand Pirouzi, Ph.D.CrownCollege
3 months agoeCTD Module 1: FDA, EMA, and Japan Requirements | ICH M4 Guidelines by Peivand Pirouzi, Ph.DGlobal Impact of (eCTD) Submissions