SPECIALIZED CLINICAL RESEARCH, PHARMACOVIGILANCE, SCIENTIFIC WRITING & AI COURSES
Specialty Course
Professional Certificate in Pharmacovigilance (PCPV)
- Introduction to Pharmacovigilance
- History of Pharmacovigilance
- Pharmaceutical Regulatory Agencies and Organizations
- New Drug Registration Process (Brief Overview)
- Drug Withdrawals and Safety Alerts
- Pharmacovigilance Methods
- Causality Assessment
- Signal Detection in Pharmacovigilance
- Guidelines and Standards Governing Pharmacovigilance
- Individual Case Safety Reports (ICSRs)
- Adverse Event (AE) Reporting Forms
- MedDRA (Medical Dictionary for Regulatory Activities)
- Aggregate Safety Reports
Specialty Course
Professional Certificate in Clinical Research (PCCR)
- Drug Development Process
- New Drug Discovery
- Clinical Development of Drug
- Essential Clinical Trial Documents
- Clinical Trials Terminology
- Good Clinical Practice (GCP)
- Ethics in Clinical Research
- Informed Consent
- Biostatistics
- Regulatory Affairs
- Roles and Responsibilities of Clinical Trial Personnel
Specialty Course
Advanced Certificate Program in Scientific Writing (SW)
- Introduction to Clinical Research
- Clinical Study Process
- Development of Standard Operating Procedures (SOPs)
- Protocol
- Case Report Form (CRF)
- Clinical Study Report
- Other Regulatory Documents
- Aggregate Safety Reports
- Publications
Specialty Course
Advanced Certificate Program in Project Management (PM)
- Introduction to Clinical Research
- Project Milestones Planning and Forecasting
- Cost Estimate and Financial Planning
- Logistics Planning, Vendor Selection and Management
- Creation of Trial Master File
- Management of Regulatory Document Submission
- Co-ordination of Individual Site Set-up Activities
- Import Export Requirements for Clinical Trials
- Organization of Investigator Training Meeting
- Study Initiation, Conduct and Milestones Tracking
- Audits and Quality Assurance
- Regulatory Inspection
- Study Closeout
Specialty Course
Advanced Certificate Program in Clinical Trial Monitoring (CTM)
- Fundamentals of Clinical Research
- Regulatory and Ethical Framework
- Clinical Trial Protocol and Documentation
- Site Management and Regulatory Compliance
- Data Management
- Pharmacovigilance and Safety Reporting
- Biostatistics Requirements
- Quality Assurance and Risk-Based Monitoring
- Clinical Supply and Logistics
- Clinical Project Management
Specialty Course
Certification in fundamentals of Artificial intelligence in Healthcare industry (AI)
- Introduction to AI in Healthcare
- Core AI Concepts
- Healthcare Data Management
- AI Applications in Healthcare
- AI in Drug Discovery & Clinical Research
- Regulatory, Ethical & Safety Framework
- Brief Note on AI Tools
- Future Trends & Workforce Transformation
Industry-Focused Training
Cynture Global is committed to delivering industry-focused training that blends theoretical knowledge with hands-on practice. Our courses in pharmacovigilance, clinical research, project management, and scientific writing are designed to enhance employability and professional competence.
Expert-Led Programs
Through our expert-led programs, students gain insights into real-world scenarios, learn regulatory compliance, master project management, and develop effective communication skills to thrive in the pharmaceutical and clinical research landscape.
Our aspects
Best Clinical Research, SW & PV Training Providers
Participants from different countries
Multiple locations across India and Other countries
Course materials from industrial experts having 10+ years experience
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