Pharma

UX-based redesign KHD 2000 – off-line Glove Testing System

Barrier systems such as isolators or RABS play a fundamental role in the protection of people and products in pharmaceutical production. Only tenths of a millimeter thick gloves are the most crucial interface in these hermetically sealed units. To ensure that barrier systems are sterile, and processes remain safe, a thorough and regular inspection of the glove integrity is vital. The regulatory requirements for gloves are strict. However, they also leave plenty of choice for suitable test methods. Many facility operators face the question as to which method is suited best for which system.

 

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A flexible leader in cartridge processing

Here’s one for the books: with almost 50 years of experience, we are the world market leader in cartridge processing. On all five continents, more than 200 Syntegon filling machines ensure safe and flexible filling of liquid pharmaceuticals into cartridges – regardless of container size and output rate.

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Filling pharmaceutical powders efficiently and safely

Pharmaceutical powders form the basis for many antibiotics that are essential for comprehensive medical care. In this interview, Markus Heinz, product manager at Syntegon, explains which changes are currently taking place in the market and which challenges antibiotic manufacturers are facing in powder filling. …more



Remote Service Assistant

Have you ever been desperately waiting for a service technician to fix any of your vital household appliances that unexpectedly stopped functioning?

This is how our customers may currently feel. While in “normal” times, they can rely on our service technicians to support them on site, many field service trips are now cancelled due to the Covid-19 travel bans. …more


Good Manufacturing Practice (GMP)

Medicinal products differentiate from other products as quality deficiencies of medicinal products may result in serious consequences for consumers. For this reason, pharmaceutical manufacturers in Europe are subject to the Directive and a supplementary Guideline to Good Manufacturing Practice (GMP). …more





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