Happy to share that on 09th January 2026, the Glow Pharma Institute successfully delivered an advanced cGMP training program with an intensive practical workshop, focused on some of the most critical quality risk areas in pharmaceutical manufacturing.
The training covered:
Deviation Management
CAPA Handling
Contamination, Cross-Contamination & Mix-Ups
The workshop was led by an experienced faculty team comprising Mr. Deepak Chatur, Mrs. Monika Kohli, and Mr. Haresh Ahuja, bringing together deep regulatory insight and extensive industry experience.
Aligned with current global cGMP expectations, the program emphasized the importance of continuous training, retraining, and quality awareness as essential pillars for sustainable compliance. Rather than conventional presentations, the sessions were designed as interactive, brainstorming-driven workshops, addressing real-time challenges faced during routine pharmaceutical operations.
Key highlights included:
Practical handling of deviations and documentation
Structured investigation methodology
Root Cause Analysis (RCA)
Detailed CAPA lifecycle – corrective actions, preventive actions, process flow, and effectiveness checks
Comprehensive understanding of contamination, cross-contamination, and mix-ups – including types, sources, risk assessment, and mitigation strategies
The training enabled participants to strengthen their right-first-time approach, improve compliance culture, and align daily practices with regulatory expectations.
✨ Glow Pharma Institute also offers customized, on-site practical workshops and cGMP training programs for pharmaceutical organizations.
Our Servives:
⚫GMP Services
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📞 Contact us:
📱 9930970226 | 9920343137
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[email protected]
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