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Contacts

Switzerland, Stein AG - 4332
Schaffhauserstrasse 30

+41 56 281 91 14

info@qps-engineering.ch

Tag: Pharma Engineering

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Harnessing AI for Aseptic Manufacturing Excellence

AI in Aseptic Manufacturing: Revolutionizing Pharma Production Invest in AI-Driven Technologies: Embrace AI solutions for predictive maintenance and environmental monitoring to enhance operational reliability and compliance. Leverage Digital Twins: Consider the implementation of digital twins to afford a better understanding of…

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Pharma and Life Sciences Strategy for 2025

Strategy for Pharma and Life Science Industry in 2025: Pioneering a Future of Innovation and Resilience The pharma industry is shifting towards innovative therapies and AI technologies. Portfolio evolution is essential, focusing on high unmet medical needs. Embracing digital transformation and…

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Navigating Challenges in Switzerland’s Pharma Sector

Recent News About the Pharma Industry in Switzerland: Navigating Challenges and Embracing Innovation Embrace Digitalization: Invest in AI and multi-omics technologies to enhance drug discovery and improve operational efficiencies. Sustainability as a Core Objective: Align business models with sustainability goals, which…

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Essential Insights on Annex 22 for Pharma Professionals

A Helpful Overview of Annex 22: Artificial Intelligence Annex 22 provides guidelines for integrating AI in pharmaceutical manufacturing. It addresses critical aspects such as model selection, training, validation, and oversight. Emphasizes the importance of data quality, explainability, and transparency in AI…

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Ensuring Safety through Aseptic Filling Validation

Qualification and Validation of Innovative Aseptic Filling Lines in Pharmaceutical Industries Develop Comprehensive Protocols: Invest in creating detailed validation protocols that cover all aspects of the aseptic filling process. Prioritize Training: Ensure personnel are well-trained and qualified, as their competence is…

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Ensuring Integrity in Pharmaceutical Facilities with NDT

Non-Destructive Testing in Pharmaceutical Facility Projects: Protecting Integrity While Maintaining Productivity NDT is key to maintaining safety and compliance in pharmaceutical facilities. Common techniques include Ultrasonic Testing, Radiographic Testing, and more. NDT supports routine maintenance and risk mitigation effectively. Automated NDT…

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Emerging Trends in Biotech Manufacturing

Trends in Biotech Manufacturing: Continuous Processes and Flexible Multi-Product Plants Continuous manufacturing enhances production efficiency and product quality. Flexible multi-product plants allow for rapid adaptation to market demands. Technological innovations are crucial for maintaining competitiveness in the biotech sector. Economic implications…

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Rethinking Qualification and Validation in Pharma

Risk-Based Approaches to Qualification and Validation: Rethinking Compliance in Pharma and Biotech Over 50% of industry professionals prioritize risk management in their strategies. Embracing risk-based approaches enhances efficiency and compliance. Core principles include risk identification, assessment, control, and continuous improvement. Regulatory…

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Enhancing Legacy Equipment for GMP Compliance

Case Study: Retrofitting Legacy Equipment for GMP Compliance Retrofitting legacy equipment offers a cost-effective solution for GMP compliance. Strategic upgrades enhance operational efficiency and data integrity. Holistic planning and design are crucial for success. Embracing Industrial Internet of Things (IIoT) can…

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Why Temperature Mapping is Vital for Pharmaceutical Integrity

Why Temperature Mapping Matters in Pharma Storage and Transport Temperature mapping is crucial for ensuring product efficacy and safety. It identifies hot and cold spots in storage areas. Temperature mapping helps prevent financial losses from spoilage. It ensures compliance with regulatory…

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