Syntegon is continuously enhancing its service portfolio to support customers even better with intelligent and sustainable services in the future. Due to the current situation, there is a growing trend towards digitalization.
Syntegon is happy to introduce the MIH-IV – a manual inspection system that provides an optimal environment for the inspection of infusion (IV) bags. …more
It was just announced that Messe Duesseldorf has cancelled interpack 2020. Save the date and visit from 7 to 13 May our virtual booth. We will bring our interpack innovations to your desk. To find out more, visit our website.
Just like we human beings, production equipment also needs a health check-up every now and then, performed by a team of specialist “doctors”.
Whether it is the output or scrap rate, set-up or handling time – packaging and processing lines have many areas where subtle problems can hide. But once a problem is recognized, how is the manufacturer to identify these hidden issues without disassembling the entire line?
We have got the answer: a “technical audit”.
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.
Self-administration of drugs on the rise
PCI Pharma Services relies on RRA assembly machine from Bosch Packaging Technology
The injectable drug delivery market has experienced a huge change in recent years. Due to drastic changes in lifestyle and the accompanying increase in chronic diseases such as diabetes, the demand for injectable drugs has been growing for decades. This transformation relates not only to the quantity, but also to the way in which injectable drugs are delivered today.
There are many things to consider when transferring products and materials into barrier systems. It begins with categorizing the pharmaceutical product and defining the aseptic environment. How is my product categorized? What processes and procedures are commonly used? What are the major challenges in product and component supply? These and many other questions are a first baseline to start with.
Quality Risk Management (QRM) is a systematic process for assessing, controlling, communicating and reviewing risks that affect the quality of a medicinal product. An efficiently implemented quality risk management system (QRM) ensures the quality of products throughout the entire life cycles and is an enabler of the Pharmaceutical Quality System (PQS). …more
Bosch Packaging Technology’s Xelum R&D for the continuous production of oral solid dosage (OSD) forms holds substantial potential: since it was first introduced to selected customers in 2018, the compact, innovative machine has attracted considerable interest. …more
(Russian Version below)
At Pharmtech in Moscow, visitors to booth B6021 (pavillion 2, hall 8) are in for a local premiere, some exciting action, an inspiring talk, as well as a few new and familiar faces.
