The industry needs a single standard cleaning limit at 25 mg/m2. At home, when washing the dishes, do we ever consider what meal they will be used for next? When plates and cutlery are taken out of ...

A lifecycle approach can be used to develop GMP-compliant cleaning procedures for continuous manufacturing of solid-dosage pharmaceuticals. It is now possible, as demonstrated by Janssen (1), for drug ...

Medical device equipment manufacturers work in an environment where product quality isn't just a competitive advantage, it's a regulatory necessity with direct implications for patient safety. As ...

The various cleaning validation processes adopted by the drug manufacturers in pharma and biopharmaceutical companies is a significant aspect in determining how safe the drugs and medical products ...

Developing a cleaning validation for a reusable medical device presents several challenges. How are you addressing them? "There have been many issues over the last 7 years, so there's increased ...

This is a practical based course. We explore the issues and pitfalls you may experience when performing Cleaning Validation. Help, guidance and training is given on techniques to overcome the issues ...

Dublin, March 02, 2022 (GLOBE NEWSWIRE) -- The "Pharmaceutical Cleaning Validation Market Share, Size, Trends, Industry Analysis Report, By Product; By Test; By Region; Segment Forecast, 2021 - 2028" ...

In 2021, the Pharmaceutical Cleaning Validation market was estimated to be worth approximately US$ 15.7 billion. With a predicted CAGR of 6.8% over the next ten years, the market is expected to be ...

The pharmaceutical industry is undergoing a transformative era driven by increasingly stringent global regulatory requirements, significantly impacting operational processes, particularly those ...