Skills and training required in the field of Research Analysis. Peivand Pirouzi, Ph.D.
33:57
Skills and training required in the field of Research Analysis. Peivand Pirouzi, Ph.D.
Health Canada CTA in CTD format: Completing the PSEAT form. Peivand Pirouzi, Ph.D.
31:18
Health Canada CTA in CTD format: Completing the PSEAT form. Peivand Pirouzi, Ph.D.
eCTD and Drug Development Lifecycle: ICH-M4, M4Q, M4S, and M4E. Peivand Pirouzi, Ph.D.
52:17
eCTD and Drug Development Lifecycle: ICH-M4, M4Q, M4S, and M4E. Peivand Pirouzi, Ph.D.
Global Regulatory Harmonization for Drugs & Medical devices- IMDRF and ICMRA. Peivand Pirouzi, Ph.D.
23:09
Global Regulatory Harmonization for Drugs & Medical devices- IMDRF and ICMRA. Peivand Pirouzi, Ph.D.
Health Canada CTA in CTD format: Clinical trial site information form.Peivand Pirouzi Ph.D.
1:04
Health Canada CTA in CTD format: Clinical trial site information form.Peivand Pirouzi Ph.D.
Health Canada CTA in CTD format: Clinical trial attestation form. Peivand Pirouzi, Ph D
0:52
Health Canada CTA in CTD format: Clinical trial attestation form. Peivand Pirouzi, Ph D
Understanding clinical responses and reporting outcomes in clinical trials. Peivand Pirouzi, Ph.D.
50:02
Understanding clinical responses and reporting outcomes in clinical trials. Peivand Pirouzi, Ph.D.
eCTD Submission Tools and Software. Peivand Pirouzi, Ph.D.
57:16
eCTD Submission Tools and Software. Peivand Pirouzi, Ph.D.
Best Practices in Preparing eCTDs. Peivand Pirouzi, Ph.D.
1:15:16
Best Practices in Preparing eCTDs. Peivand Pirouzi, Ph.D.
Writing an ISO9001/13485, and QSR 21CFR820.3k compliant Quality Manual. Peivand Pirouzi, Ph.D.
1:09:14
Writing an ISO9001/13485, and QSR 21CFR820.3k compliant Quality Manual. Peivand Pirouzi, Ph.D.
Container Closure System Characteristics and Testing for Pharmaceuticals. Peivand Pirouzi, Ph.D.
1:03:07
Container Closure System Characteristics and Testing for Pharmaceuticals. Peivand Pirouzi, Ph.D.
Nano-Technology and Human Health. Peivand Pirouzi, Ph.D.
1:22:46
Nano-Technology and Human Health. Peivand Pirouzi, Ph.D.
Reporting, Identification, and Qualification of impurities: ICH-Q3A to Q3D. Peivand Pirouzi, Ph.D.
54:45
Reporting, Identification, and Qualification of impurities: ICH-Q3A to Q3D. Peivand Pirouzi, Ph.D.
IND preparation and submission to FDA through Electronic Submission Gateway. Peivand Pirouzi, Ph.D.
1:27:39
IND preparation and submission to FDA through Electronic Submission Gateway. Peivand Pirouzi, Ph.D.
Scientific Assessment in Clinical Research: Data Management and Data Visualization. P.Pirouzi,Ph D
16:51
Scientific Assessment in Clinical Research: Data Management and Data Visualization. P.Pirouzi,Ph D
Medical Device Design History File (DHF) Audit checklist. Peivand Pirouzi, Ph.D
16:17
Medical Device Design History File (DHF) Audit checklist. Peivand Pirouzi, Ph.D
Medical Devices Design Requirements by FDA. Peivand Pirouzi, Ph.D.
8:07
Medical Devices Design Requirements by FDA. Peivand Pirouzi, Ph.D.
CAPA (ISO9001 and QSR) and Responding to FDA Warning Letters. Peivand Pirouzi, Ph.D.
52:44
CAPA (ISO9001 and QSR) and Responding to FDA Warning Letters. Peivand Pirouzi, Ph.D.
Health Canada and FDA regulations for Tissue Engineering Peivand Pirouzi, Ph D
38:48
Health Canada and FDA regulations for Tissue Engineering Peivand Pirouzi, Ph D
Ethics on Stem Cell Therapy. Peivand Pirouzi, Ph.D.
51:34
Ethics on Stem Cell Therapy. Peivand Pirouzi, Ph.D.
Principles of Pharmaceutical Analytical Methods and Validation: ICHQ2 & Q6A. Peivand Pirouzi, Ph.D.
1:08:52
Principles of Pharmaceutical Analytical Methods and Validation: ICHQ2 & Q6A. Peivand Pirouzi, Ph.D.
FDA-NIH database: Dailymed and the structure of a pharmaceutical product label.Peivand Pirouzi,Ph.D.
50:33
FDA-NIH database: Dailymed and the structure of a pharmaceutical product label.Peivand Pirouzi,Ph.D.
Personalized and Precision Medicine and Key FDA Regulations. Peivand Pirouzi, Ph.D.
1:05:50
Personalized and Precision Medicine and Key FDA Regulations. Peivand Pirouzi, Ph.D.
Medical Devices Design Control and Development Planning. Peivand Pirouzi, Ph.D.
1:08:10
Medical Devices Design Control and Development Planning. Peivand Pirouzi, Ph.D.
US and EU Pharmacopeia Standards for Pharmaceutical Products. Peivand Pirouzi, Ph D.
15:55
US and EU Pharmacopeia Standards for Pharmaceutical Products. Peivand Pirouzi, Ph D.
Pharmaceutical Manufacturing Process for Mammalian Cell Culture. Peivand Pirouzi, Ph D.
55:30
Pharmaceutical Manufacturing Process for Mammalian Cell Culture. Peivand Pirouzi, Ph D.
Clinical Trials Information System in Europe (EMA-Clinical Research). Peivand Pirouzi, Ph.D.
32:39
Clinical Trials Information System in Europe (EMA-Clinical Research). Peivand Pirouzi, Ph.D.
FDA databases: Drugs@FDA and Clinical trials.gov - Live demonstrations - Peivand Pirouzi, Ph.D.
53:16
FDA databases: Drugs@FDA and Clinical trials.gov - Live demonstrations - Peivand Pirouzi, Ph.D.
FDA Guidance on Formal Meeting Requests for Prescription Drugs' Applications. Peivand Pirouzi, Ph.D.
1:13:55
FDA Guidance on Formal Meeting Requests for Prescription Drugs' Applications. Peivand Pirouzi, Ph.D.
Pharmaceutical Inspections and Audits:GMP, GCP, & Pharmacovigilance (ICHE2A-E2F). P.Pirouzi, Ph.D.
1:06:53
Pharmaceutical Inspections and Audits:GMP, GCP, & Pharmacovigilance (ICHE2A-E2F). P.Pirouzi, Ph.D.