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AUTOMA+ 2025: anic GmbH Sets New Standards as Gold Sponsor in Austria
AUTOMA+ 2025: The future of pharma starts now – join us!…
AUTOMA+ 2025: The future of pharma starts now – join us!…
Audit trail reviews are more than a mandatory exercise – they are crucial for data integrity and compliance in pharmaceutical manufacturing. Yet in practice, many companies face hurdles: unclear raw data, missing filters, and time-consuming manual checks.…
The pharmaceutical industry is facing major challenges: Strict regulations (validation, ER/ES, audit trail, data integrity, data consistency, etc.) must be met, while at the same time customers expect innovation, fast delivery times and a broad product range – all while maintaining consistently high, defined quality – What if the first step to solving your challenges could be found in this article…?…
Create GxP-compliant EBR recipes in minutes instead of months! Read this blog post to find out why anicomply is the benchmark for flexibility in electronic batch recording software in the chemical and pharmaceutical production environment.…
Today’s IT world is getting more and more complex. Companies are dependent on using software, which is connected to the internet. While cyberattacks spread, it is becoming a real challenge making sure, that software is truly secure. The right way to go is an industry best practice Secure Software Development Lifecycle.…
Read more about the key to secure software development here.
The challenge: an existing storage system for chemicals was expanded. Large parts of the items were to be relocated to a newly built warehouse with dynamic warehousing and automated delivery systems. To do this, it was necessary to re-label the items with new barcodes. How do you simplify the migration of thousands of inventory items?…
