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Pharmacovigilance Course
Introduction of Pharmacovigilance
Overview of Pharmacovigilance
Standard Terms and Terminology in Pharmacovigilance
Medical Evaluation of Adverse Events
Adverse Event Reporting System and Form
Diagnosis And Managements of ADRs
Medical Evaluation of AE
Case Processing Global Perspective of Pharmacovigilance
Single Case Processing
Case Narrative Writing
Pharmacovigilance Reporting Database
Signal Detection
Managements and Risk Assessments
Evaluation Quality System In PV
Expedited Reporting Criteria
PSUR & PBRER
PV Database and Signal Detection
Risk Assessments & Managements
Medical Dictionary for Regulatory Activities medDRA
PV laws And Guideline Regulatory Guideline & Laws In PV
SOPS In PV
PV Auditing and Inspection
Regulatory Aspects In PV
Clinical Data Management Courses
Introduction to Clinical Research
Roles and Responsibilities
Introduction to Data Management
Case Report Form (CRF) Design
Creating Reports and Transfer Data
Identifying and Managing Discrepancies
Data Entry & Remote Data Entry
Collecting Adverse Event Data
Data Management Plan Tracking CRF Data
Recreating Reports and Transferring Data
Clinical Research and Regulatory Submissions
Clinical Submissions
Planning for Clinical Trials
Electronic Data Capture
Managing Lab Data
Clinical Research Courses
Introduction of Clinical Research
Essential documents in Clinical Research and Regulatory Requirements
Indian Regulation Domestic Regulation
Study Setup Process
QC, Compliance & Auditing in Clinical Research
Clinical Trial Design and Project Managements
Clinical Monitoring
Principles of Good Clinical Practices
Biostatistics and SAS Courses
Biostatistics and SAS Courses
Drug Regulatory Affairs and IPR Courses
Pharmaceutical Industry Courses
Medical Writing Courses
Technical Aspects of Medical Writing
Drug Discovery and Development
ICH Guidelines
CTD Modules
Basics of Statistics and Research Methodology
Introduction to Style Guides
Grammar and Scientific Language
Hands-on Activities Related to Style Guide
Introduction to Narrative Writing and Hands-on Exercises
Introduction to Publication Writing
Systematic Literature Reviews
Meta-analyses
Decoding Clinical Study Protocol
Clinical Study Reports and Hands-on Activities
Quality Assurance Courses
Pharmaceutical Analysis
Quality Assurance Techniques
Drug Regulatory Affairs
Good Manufacturing Practices
Pharmaceutical materials science
Quality management system
Dossier preparation and submission
GCP Training Courses
Healthcare Courses
Overview on Public Health Systems and Policy
Healthcare Quality Standards
Quality Management, Tools and Techniques
Hospital Operations planning and Management
Statistics for Healthcare Quality
Hospital and Patient Safety
Key Stakeholders in Clinical Research
Medical Devices Courses
Medical Imaging & Processing
Medical Instrumentation
Biosensors
Computer Application (CAD & CAM)
Biostatistics
Fundamental Intellectual Property (IP) and Technology Management
Medical Instrumentation Laboratory
Pre-clinical Studies Laboratory
Bioengineering and regenerative devices
Drug Delivery Engineering
Biomaterials
Biomedical Signal Processing
Artificial Intelligence in Medical Devices
Regulatory in Medical Devices
Bio and Pharmaco-engineering Laboratory
Biomedical devices Laboratory
Medical devices Testing Laboratory
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