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"Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)" Seminar has been added to ComplianceOnline.coms offering.

Image courtesy of Pixabay Representative image Powder & Bulk Solids examines the current status of America’s cannabis processing and infused products manufacturing businesses. The COVID-19 pandemic highlighted a number of industries strengths and weaknesses as the world’s manufacturers faced supply chain interruptions, staffing issues, shutdowns, transportation issues and more. In many ways, the crisis has offered the cannabis industry to demonstrate its resiliency...

Small-scale models (SSMs) are widely used in the biopharmaceutical industry. These models are used for process development and optimization,...

Kneat Announces Selection by Top Ten Biopharma as the Corporate Solution for Global Manufacturing and Provides an Update on its Recent Financing News provided by Share this article LIMERICK, Ireland, May 7, 2021 /CNW/ -  kneat.com, inc. (TSX-V: KSI) ("Kneat") announces it has signed a five-year corporate Master Services Agreement (MSA) with another top ten biopharma company, and provides an update on its recent financing.   Top Ten Biopharma Selects Kneat as its Corporate Validation Platform ...

FDAnews Announces Process Validation for Devicemakers: Concepts, Methods and Models Management Report Share Article Does one’s device’s process validation program stand up to FDA scrutiny? Ensure compliance with these strategies and methods. Order today. WCG FDAnews Process Validation for Devicemakers: Does one’s process validation program stand up to FDA scrutiny? Process Validation for Devicemakers: Concepts, Methods and Models is a must to ensure medical devices are compliant. This ...