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We are enhancing our smart equipment portfolio with IoT-enabled control systems and cloud connectivity
Express Pharma
|December 2025
In an interaction with Express Pharma, Dr Manoj Chaudhari, Managing Director, Mack Pharmatech Pvt. Ltd., highlights the company's focus on digitalisation and compliance-driven innovation, detailing how their next-generation smart stability chambers, cold rooms, and ultra-low freezers are being designed to meet the evolving demands of Pharma 4.0 and advanced therapy applications
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What key industry trends are visible at CPHI this year, and how is your company positioning itself in response?
Trend at CPHI:
• The pharma sector is rapidly adopting digitalisation, AI, and IoT— from manufacturing through QC and stability testing.
• Companies are investing in smart, connected lab environments for real-time monitoring, predictive maintenance, and data integrity compliance (especially with FDA 21 CFR Part 11 and EU Annex 11).
• Growth in biologics, cell, and gene therapies is creating new needs for precise temperature and humidity control, especially for biologic sample storage, stability, and transport validation.
Mack Pharmatech's positioning:
• We are enhancing our smart equipment portfolio with integrated data-logging, IoT-enabled control systems, and cloud connectivity.
• Our latest stability chambers and cold rooms feature real-time remote monitoring, automated alarms, and data security features.
• We are collaborating with automation specialists to ensure our products fit seamlessly into digital QC and stability workflows.
• We're developing customised stability and cold-chain simulation systems for biologics and vaccine testing.
• Our ultra-low temperature freezers and precision cold chambers are validated for advanced therapy applications.
• Every Mack Pharmatech system is delivered with comprehensive DQ/IQ/OQ/PQ documentation, traceable calibration, and data-integrity compliant software.
• We've built an internal compliance and validation support team to assist customers during audits and regulatory submissions.
• We are integrating Part 11-compliant digital interfaces for secure audit trails and electronic record management.
How has CPHI influenced your product or market strategy over time?
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