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Pharma & Biotech

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Insights

VIDEO: Understanding Commissioning, Qualification & Validation (CQV)

Smarter CQV starts early. Jay Tarter, Mosh Morton, and Tulsa Scott share how risk-based planning and continuous testing keep healthcare and pharma projects compliant and on track.

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Insights

Continuous manufacturing in pharma: what facility leaders need to know before committing

Continuous manufacturing offers speed and consistency, but it changes everything from validation to utilities. Here’s what leaders need to know.

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Insights

VIDEO: Digital twins in pharma

Salas O’Brien experts John Glenski, Julie Hoffherr, Josh Morton, and Todd Plymale explain how digital twins boost pharma decision velocity, reduce risk, and streamline manufacturing.

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Insights

Planning for FDA PreCheck: what clients need to know

FDA PreCheck introduces a proposed two-phase pathway to accelerate US drug manufacturing. Learn what it means for design, compliance, and project planning.

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Insights

Geothermal strategies for decarbonizing energy-intensive pharma sites

What pharmaceutical facilities across the US and Canada need to know about using geothermal strategies to cut emissions, lower long-term costs, and support corporate sustainability goals.

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Insights

The CQV crunch: how to keep schedules on track when time is not on your side

In life science projects, early CQV integration prevents costly delays by catching validation issues before they impact schedules or compliance

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Insights

Risk registers for pharmaceutical manufacturing

Proactive risk management can prevent costly recalls, legal issues, and damage to brand reputation for pharmaceutical manufacturing. By implementing effective risk registers, pharmaceutical companies can protect their bottom line, maintain market competitiveness, and easily respond to regulatory compliance.

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Insights

Robotics and aseptic manufacturing in pharmaceuticals

Discover how robotics and automation are revolutionizing aseptic manufacturing processes, helping pharmaceutical manufacturers maintain high standards of safety and efficiency in an increasingly competitive market.

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Insights

Advancing sustainable delivery in pharmaceutical manufacturing

This article explores the challenge of maintaining effective operations while advancing the transition to sustainable practices. We also cover options to produce consistent, incremental improvements that can produce big cumulative results.

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Insights

Creating flexibility and resilience in life science research facilities

Structural engineering for life science research labs is complex. This article highlights the issues research facilities face in creating resilience, and how smart structural design can deliver solutions.

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    Maria Kordjamshidi explores how to deliver low-carbon laboratory buildings at the 2026 SLCan Sustainable Laboratory Conference

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