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PCI – 7th June 2024
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Nipro April 2026
Volume 16 Issue 1

Why is Real World Data the Key to Rare Disease Success?

The quest to understand and treat rare diseases is among the most challenging and vital missions in healthcare today. As the industry seeks innovative solutions, Rea...
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Volume 16 Issue 1

Advancing Therapeutic Solutions with Antibody-drug Conjugates (ADCs)

As promising therapeutic agents for treating oncology indications, antibody-drug conjugates (ADCs) have become prominent in the biopharmaceutical market in recent ye...
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Volume 16 Issue 1

Generative AI and its Impact on Speed to Market for Pharmaceuticals

Did you know that it takes approximately seven years to develop and bring a new drug to market? However, this time can be significantly reduced by months or even yea...
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Volume 16 Issue 1

The End to Painfully Slow Cloud Migration?

Despite the benefits of moving to the cloud, migration can still be prohibitively time-consuming and costly, especially in a highly regulated industry like pharma. B...
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Volume 16 Issue 1

Reaching the Marketplace

Understanding the Complexities of Paediatric Drug Development and Manufacturing Bringing a paediatric drug product to the marketplace can be very complex and also...
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Volume 16 Issue 1

The Future of Sterility

Advancements and Innovations in Sterile Drug Product Manufacturing Sterile drug product manufacturing is complex and plays a crucial role in the pharmaceutical in...
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Automating Biotherapy Production at the Speed of Market Expansion
Volume 16 Issue 1

Automating Biotherapy Production at the Speed of Market Expansion

The effort to scale biotherapy production and meet the demand for personalised medicine is well underway, and robotic automation is taking on an ever-expanding role....
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Volume 16 Issue 1

The Key to Formulation Development is in the Details

During the tablet manufacturing process, tooling and press manufacturers are often faced with ongoing challenges. As a tooling and press manufacturer, you should be ...
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Volume 16 Issue 1

Biocompatible, Pre-coloured and Sustainable ABS Optimised for Laser-marking to Support Medical UDI Identification along with Sustainability Targets

The EU’s Medical Device Regulation (MDR) and US’ Code of Federal Regulations Title 21, about the labelling of medical devices (21 CFR 801 Subpart B), require a Uniqu...
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Volume 16 Issue 1

Safety, Compliance and Quality Just a Click Away

The Crucial Role that Automated Print Inspection Systems Can and Should Play in Pharmaceutical Packaging. Producing safe and compliant medicines – and harmless co...
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SMI London
Biopharma group march 2026
Interpack Staubli March 2026
Silgan March 2026
Scott Pharma – 25.03.2025
Bespak – 21.05.2025
Aptar – 08/01/2026
Stoelzle – 15th May 2025
L.B. Bohle – 08.04.2025