Essayer OR - Gratuit
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?
Cette histoire est tirée de l'édition December 2025 de Express Pharma.
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