“We need uninterrupted and reliable monitoring, because in a single refrigerator we can lose material worth more than 10,000 euros,” says Freese. “Not to mention the delay in development when it comes to blood samples from clinical trials.”
Quality and safety in drugs production is the overriding concern. Now regulators are tightening their grip on the integrity of all the data produced. In the pharmaceutical industry, regulations require close monitoring of the manufacturing and logistics of drugs to guarantee their quality, safety anAlready a subscriber Login You have…
Continuous monitoring of an environment with a sensor during bio-decontamination allows you to decrease the number of indicators used in routine processes because there is accurate inline measurement data available. Chemical indicators (CI), biological indicators (BI) and enzyme indicators (EI) aAlready a subscriber Login You have read all your free…
Spot-checking is a less time-consuming process than calibration, in part because the calibration process can include as-found data, adjustment (if necessary), and as-left data whereas spot-checking is a verification that the unit under test is still within specification. Field spot-checking is a Already a subscriber Login You have read all…
Connect in Pharma is promoting a new era of cross-sector collaboration within the pharmaceutical industry. The newly announced agenda for Connect in Pharma sends a strong message for more cross-sector collaboration. Technology gurus, consultancy experts and motivational speakers from a wide rangeAlready a subscriber Login You have read all your…