Become a High-Performance Drug Safety Professional
Master the complete Individual Case Safety Report (ICSR) lifecycle — from triage and intake to USFDA, EMA, and CDSCO regulatory submission — using authentic industry workflows and databases.
Seats are limited per batch. Early registration recommended.
Program Overview
The Advanced Masters Certification in Pharmacovigilance & Drug Safety is the definitive industry-standard program for professionals who are serious about mastering drug safety operations at the highest level. This is not a survey course. It is a rigorous, practitioner-designed program that takes you through every phase of the ICSR lifecycle using the exact workflows, systems, and decision logic used by drug safety teams at top pharmaceutical companies and CROs worldwide.
From Oracle Argus Safety navigation and advanced MedDRA coding to causality assessment, narrative mastery, and multi-regional regulatory submissions, every module maps directly to real tasks performed in regulated pharmaceutical environments. Graduates leave not just knowledgeable — but operationally ready.
Why Global Pharmacovigilance Academy?
Every session is delivered by working PV professionals, not academics. You learn the decisions, workflows, and judgment calls that define high-performance drug safety.
You don't just learn about case processing — you work through it. Real intake, real triage, real MedDRA coding logic, real regulatory timelines.
Navigate real safety database architecture and case lifecycle management — the #1 system used in global pharma and CRO environments.
USFDA, EMA, and CDSCO reporting requirements covered in dedicated modules — not as footnotes. You'll know what to submit, when, and how.
Is This Program Right for You?
Week-by-Week Curriculum
Each week combines structured knowledge with practical, industry-aligned application.
- Global PV ecosystem — WHO, ICH, FDA, EMA, CDSCO
- ICH guidelines: E2A, E2B(R3), E2C, E2D, E2F applied
- GVP modules overview and compliance mindset
- Drug safety obligations across the product lifecycle
- Spontaneous vs solicited report classification
- Four minimum valid case criteria in depth
- Seriousness criteria — regulatory definitions applied
- Triage logic and case prioritisation workflows
- Patient and reporter demographic data standards
- Drug information capture: dose, indication, dates
- Data quality, completeness checks, and follow-up
- Entry standards across global safety databases
- Argus architecture, module navigation, case creation
- Routing, workflow management, and case lock
- Argus LAM for local affiliate reporting
- Audit trail management and data integrity
- SOC, HLT, PT, LLT hierarchy — deep dive
- Coding complex multi-event cases accurately
- Primary vs secondary SOC assignment rules
- Version management and quality review standards
- WHO-UMC and Naranjo causality methods
- Expectedness vs reference safety information
- Listedness against Company Core Data Sheet
- Regulatory-quality narrative writing structure
- IND Safety Reports: 7-day and 15-day rules
- MedWatch 3500A and FAERS submission protocols
- NDA/BLA post-marketing expedited reports
- FDA inspection expectations for PV teams
- EudraVigilance submission requirements
- EU QPPV responsibilities and PV system
- ICH E2B(R3) electronic message structure
- SUSAR reporting under EU Clinical Trial Regulation
- CDSCO Schedule Y and Form 12A requirements
- Indian Pharmacovigilance Programme (IvIPC)
- ASEAN, PMDA, TGA regional PV requirements
- Multi-regional submission calendar management
- PBRER structure and ICH E2C(R2) compliance
- Benefit-risk framework — methodology and language
- Data lock point and reporting interval logic
- PSUR submission to EMA and regional adaptations
- PRR, ROR, EBGM quantitative detection methods
- Signal evaluation, triage, and escalation logic
- Risk Management Plan structure and content
- Additional Risk Minimisation Measures (aRMMs)
- PV career ladder: DSA to Global PV Head
- Advanced resume architecture for senior roles
- Technical interview mastery: case-based scenarios
- LinkedIn positioning for global PV recruitment
What You Will Be Able to Do
By the end of this program, you will:
What Roles Can You Target After This Program?
Mid-Level Roles
- Drug Safety Specialist
- ICSR Team Lead
- MedDRA Coding Lead
Senior / Strategic Roles
- PV Case Processing Manager
- PV Compliance Specialist
- Global Drug Safety Manager
- Pharmacovigilance Lead
- Signal Management Specialist
- Regulatory PV Strategist
- Safety Operations Head
Global Opportunities
- CRO Safety Operations (Global)
- Pharma MNC Drug Safety Roles
- Regulatory Agency Positions
- ICSR Outsourcing Partners
- Global PV Service Providers
Frequently Asked Questions
This is an advanced program for pharmacy graduates, life sciences professionals, and working drug safety associates who want to master PV operations at the level demanded by pharma MNCs and global CROs. It is not an introductory course — it goes deep.
A basic understanding of pharmacovigilance is helpful, but not mandatory. Participants with strong science backgrounds who are motivated to master the subject from first principles perform very well. Our faculty calibrate instruction to the cohort.
The certification is issued by Global Pharmacovigilance Academy and is recognised by employers in India, the GCC, Southeast Asia, and globally. The curriculum is fully aligned with ICH, GVP, and regulatory standards used by USFDA, EMA, and CDSCO.
Batches are intentionally small — limited seats per intake. Every participant gets direct access to mentors for Q&A, case reviews, and career guidance. You are not a number in a large cohort.
Yes. Recorded session access is available for 6 months post-completion, so you can revisit complex topics, revise before interviews, or stay sharp as you transition into your new role.
GPA's curriculum is built around job-relevant skills. Week 12 is dedicated to resume building, interview preparation, and career positioning. Graduates have secured roles at pharma companies, CROs, and regulatory consulting firms in India and internationally.
Enroll in Advanced Masters Certification in Pharmacovigilance & Drug Safety
Limited seats per batch. Industry-led. Certification upon completion.
admissions@globalpva-edu.com
globalpva-edu.com
Domestic Students (India)
₹39,999
International Students
$1,499
*Fees include examination & certification charges.