A well-trained workforce is the foundation of GMP compliance. Our practical, role-specific training programs help pharmaceutical organizations strengthen technical competency, improve regulatory awareness and reduce compliance risks through interactive, industry-focused learning.
What We Deliver
- GMP Fundamentals — Training on GMP principles, personnel responsibilities and regulatory expectations.
- Revised Schedule M Training — Practical implementation of the revised Schedule M requirements.
- WHO-GMP & PIC/S Awareness — Overview of international GMP expectations and inspection requirements.
- Quality Risk Management (ICH Q9) — Risk identification, assessment, control and review methodologies.
- CAPA & Deviation Investigation — Root cause analysis, investigation techniques and effective CAPA implementation.
- Good Laboratory Practices (GLP) — Quality practices applicable to QC laboratories.
- Internal Auditor Training — Preparing employees to conduct effective GMP internal audits.
- Regulatory Inspection Readiness — Preparing teams for CDSCO, WHO, EU-GMP and US FDA inspections.
Our Approach
01
Training Needs Assessment
Understand your products, facility, departments, compliance status and learning objectives.
02
Course Customization
Develop role-specific training modules using your SOPs, processes and regulatory requirements.
03
Interactive Training Delivery
Conduct instructor-led classroom, virtual or on-site training using practical case studies and real GMP scenarios.
04
Assessment & Continuous Learning
Evaluate participant understanding through assessments, provide training records and recommend refresher training programs.
Who this is for
Production PersonnelQA ProfessionalsQC AnalystsWarehouse PersonnelEngineering TeamsValidation TeamsRegulatory Affairs ProfessionalsSenior ManagementInternal AuditorsContract Manufacturing Organizations
Why Choose Vaayath
- Customized training using your SOPs
- Trainers with extensive pharmaceutical regulatory experience
- Practical case-study-based learning
- On-site and virtual delivery options
- Role-specific modules
- Training aligned with current regulatory expectations
- Post-training assessments and competency evaluation
Training Topics
GMP Fundamentals
Revised Schedule M
New Drug approval
WHO-GMP
GDP
Data Integrity
ALCOA+
CAPA
Deviation Investigation
Change Control
Risk Management
Internal Audit
Complaint Handling
Product Recall
Available Training Formats
Classroom Training
On-site Training
Virtual Instructor-Led Sessions
Workshop-Based Learning
Refresher Programs
Mock Inspection Exercises
Executive Awareness Sessions