Information Technology

Each stage of IT implementation is driving toward adopting up to date world class processes and systems. At every stage of drug discovery, development and delivery are innovative technologies key to assisting regulatory compliance issues and organization optimization.

The European issue is not whether IT can foster business growth but how it can help companies to achieve their goals speedily.

Critical elements of Information technology are already in play in most IT savvy institutions. Next Generation Pharmaceutical is designed to aid specific purchasing and strategic decisions that will allow flexibility to accommodate future requirements

Focus Issues

-Compliance and Regulatory issues (FDA / GAMP)
-Standardization
-Manufacturing Execution Systems
-Process Control and Automation
-IT Platform Integration
-Content and Document Management
-Grid Computing

 

Banking on it
Will we ever realise the full potential of biobanks?
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Ask the expert: Bioinformatics
Simon Smith, Head of Bioinformatics at J&J, on growth and potential breakthroughs
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The stamp of approval
Recent changes have been made to the European Medicines Agency to speed up the process of advice and ensure the efficiency of application assessment ? good news in these times of pandemic panic.
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The case for intelligent clinical trials processing
A few years ago, two leading companies in a highly regulated industry were faced with the need to improve efficiency and reduce costs for a mission critical, but not differentiating, business process.
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Optimising efficiency with electronic regulatory submissions
A large generic pharmaceutical company wants to maximise ROI on R&D, but how?
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Q&A: Informatics
With Professor Antony N. Davies, Waters Informatics
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Waters - pharmaceutical discovery, development and manufacturing solutions
To bring a new product to market - and to maintain quality after the product's release - pharmaceutical companies must manage many factors for success.
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A touch quicker
A look at Braille labelling for pharmaceutical products.
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Tips for document management
By Patricia Santos-Serrao, QUMAS Senior Regulatory Affairs Consultant
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The content and compliance issue
Kevin O' Leary finds a way through the mess.
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Getting more out of your quality management system
Today's leading global pharma, biotech, and medical device companies realise their QMS requirements can no longer be fulfilled, unless the solution includes a business rule engine that automates the many processes involved in managing all quality events.
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SQL LIMS software enables seamlessly integrated paperless laboratory
SQL*LIMS® software enables AstraZeneca to reduce data review and operate a seamlessly integrated paperless laboratory
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Delivering innovation, integration, and automation to the life sciences
Corporate Profile: Applied Biosystems
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