Pharma
Cleanrooms Contamination
Control India Summit
2025

India's pharma cleanroom market is witnessing strong growth, driven by the expansion of pharmaceutical and biotech sectors, stricter regulations, modular cleanroom adoption, and a growing focus on sustainability. With the pharmaceutical industry expected to grow from USD 50 billion in FY 2023 - 24 to USD 120 - 130 billion by 2030, and the biotech sector projected to hit USD 150 billion by 2025, the demand for advanced cleanroom infrastructure is rising rapidly.
Cleanrooms are essential for ensuring product sterility, regulatory compliance, and patient safety. The market is expected to grow at a CAGR of 6.4% (2022 - 2028), supported by increased R&D, healthcare infrastructure, and smart cleanroom solutions aligned with global standards like FDA, EU GMP, and ISO 14644.
However, challenges such as high CAPEX, regulatory complexity, and a skilled workforce shortage remain. Still, cleanroom development is a strategic imperative for India's goal of becoming a global pharma hub. The Pharma Cleanroom & Contamination Control India Summit will explore the latest innovations, regulations, best practices, and future trends shaping the cleanroom industry.

THOUGHT LEADERS

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TOPIC HIGHLIGHTS

  • Evolving regional and international cleanroom regulations: Navigating compliance across regulatory bodies (EU GMP Annex 1, US FDA & WHO)
  • ISO 14644-4:2022 - Smart strategies for your greenfield/brown field cleanroom design, construction & start-up
  • Bridging the skill gap: Building a competent workforce for India's evolving cleanroom ecosystem
  • HVAC system design for cleanrooms: Precision engineering for airflow, filtration & environmental control
  • Cleanroom automation: balancing CAPEX and OPEX in the age of smart manufacturing
  • Robotic process automation (RPA) in GMP zones - Enhancing compliance, precision & efficiency

KEY TAKEAWAYS

  • Gain insights into evolving global standards like EU GMP Annex 1, ISO 14644, and FDA aseptic processing guidelines.
  • Gain valuable knowledge from industry leaders representing top brands
  • Learn best practices and new technologies for maintaining sterility and minimizing particulate and microbial contamination
  • Discover how innovations like isolators, VHP systems, real-time monitoring, and robotics are transforming cleanroom operations
  • Understand how optimized cleanroom design, validation, and monitoring can reduce risk, lower operational costs, and improve productivity
  • Connect with Engineering and project heads, QA/QC leaders, cleanroom designers, regulators, and solution providers shaping the future of pharma manufacturing

WHO WILL YOU MEET?

Functional Heads Of:

  • Quality Control
  • Quality Assurance
  • Engineering
  • Site Head
  • Factory Head
  • Project Management

WHY SHOULD YOU ATTEND?

  • Gain first-hand insights from industry leaders, regulators, and cleanroom professionals on compliance, innovation, and best practices
  • Explore the latest advancements in cleanroom design, HVAC, filtration, automation, and environmental monitoring systems
  • Understand evolving global regulations like ISO 14644, EU GMP Annex 1, and FDA guidelines, and how to maintain audit readiness
  • Dive into real-world strategies for particulate and microbial control, cleaning validation, standardized procedures and practices, and risk assessment
  • Leave with checklists, case studies, and proven approaches that can be immediately applied to optimize cleanroom operations and compliance