Training & Upskilling Programs

In the pharmaceutical industry, compliance begins with people. Even the most robust systems fail without trained, aware, and accountable professionals

At InPharma Solutions, we design structured, practical, and industry-aligned training programs that strengthen regulatory understanding, improve operational excellence, and build a culture of quality. We don’t just deliver training - We build competent, inspection-ready teams

cGMP Training

Current Good Manufacturing Practices (cGMP) are the backbone of pharmaceutical quality systems. Sessions are practical, real-case oriented, and aligned with global regulatory expectations. We focus on transforming GMP knowledge into daily practice

Our cGMP training programs are designed for:

• Manufacturing teams
• Quality Assurance & Quality Control professionals
• Engineering & Maintenance teams
• Warehouse & Distribution personnel
• Senior management

Training modules cover:

• GMP fundamentals & global expectations
• Documentation practices & GDP
• Deviation, CAPA & Change Control
• Data Integrity principles
• Audit preparedness
• Quality Risk Management

Data Integrity Training

Data Integrity is one of the most scrutinized areas during regulatory inspections. We help organizations shift from reactive correction to proactive data governance because integrity is not just about systems - it is about mindset

Our structured programs cover:

• ALCOA+ principles
• Audit trails & electronic records
• Common Data Integrity violations
• Laboratory and manufacturing data risks
• Investigation of data discrepancies
• Regulatory expectations (USFDA, EU GMP, WHO)
• Building a culture of transparency

CSV / CSA Training

With increasing digital transformation, organizations must understand validation beyond documentation. These programs are designed for QA, IT, Automation, and Validation teams. We bridge the gap between regulatory expectations and technical execution

Our CSV/CSA training programs include:

• Fundamentals of Computer System Validation
• GAMP 5 principles
• Risk-based validation approach
• Transition from CSV to CSA
• 21 CFR Part 11 & EU Annex 11 expectations
• Audit trail review practices
• Spreadsheet validation awareness
• Vendor qualification for software systems

Corporate Training

Every organization has unique operational challenges. Our programs are interactive, case-driven, and designed to deliver measurable improvement. We align training with business growth and regulatory sustainability

Our corporate training programs are customized based on:

• Organization size
• Regulatory exposure
• Recent audit observations
• Digital maturity
• Department-specific needs

We provide:

• Leadership quality workshops
• Audit readiness bootcamps
• Investigation excellence programs
• Quality culture transformation sessions
• Risk Management workshops

Student Programs

As part of our commitment to industry development and social responsibility, we provide structured programs for students and early-career professionals. We focus on empowering students with practical, industry-relevant knowledge - especially supporting aspirants from developing regions seeking affordable, high-quality training. We believe in building the next generation of compliant professionals

These programs include:

• Industry-oriented GMP fundamentals
• Basics of QA, QC, RA, and Validation
• Resume-building workshops
• Interview preparation sessions
• Practical exposure to documentation systems
• Career transition guidance (R&D to QA/RA/Validation)