Minimising Fibre Contamination in Injectable Manufacturing with MiraWIPE Wipers
Fibre contamination remains one of the most persistent and costly quality challenges in sterile injectable manufacturing. In environments where sterile drug products such as injectables must comply with strict standards like USP <790> and <1790>, the presence of visible particles, especially fibres, poses a serious risk to product integrity and patient safety. Common Sources of […]
Grover Holdings CCIT and Cleaning Takeaways from PDA Conference 2025 Hyderabad
The Parenteral Drug Association (PDA) India Chapter hosted its 2025 Annual Conference in Hyderabad in late July, drawing over 600 pharmaceutical industry experts for an engaging three-day event. Recognised as a leading authority in container closure integrity testing (CCIT), headspace analysis, clean room contamination control, and facility maintenance solutions, we were invited by the organisers […]
Cleaning Sticky Residues in Softgel Production Lines
Softgel manufacturers are familiar with the difficulties associated with cleaning gelatin build-up, plasticizers, oils and pigments. Removing these tough residues from stainless steel equipment poses a significant challenge in turnaround times and operational efficiencies. Conventional cleaning techniques like traditional wipes and standard detergents often fail to tackle heat-cured or sticky contaminants effectively. To overcome these […]
Establishing and Validating the Lifecycle of Cleanroom Gowning
Cleanroom environments demand rigorous contamination control with gowning protocols playing a pivotal role in safeguarding product integrity and operator safety. As guided by Annex 1, a critical aspect of gowning management is establishing and validating the lifecycle of cleanroom garments. This process ensures that garments maintain their protective performance throughout their use, balancing safety, comfort […]