The main purpose of Quascenta’s recently launched software application – eResidue – is to replace spreadsheets. Spreadsheets require manual input; they can suffer from calculation errors and there are ...

In pharmaceutical manufacturing, cleaning validation is an essential stage of verifying that the manufacturing process is suitable. As an integral stage of the cleaning validation program, analytical ...

Abstract Continued process verification (CPV) for a cleaning validation (CV) program begins once the validation study is complete. Planning for the CPV needs to be considered, however, as the cleaning ...

ValGenesis, Inc., the market leader in digital validation lifecycle management solutions, announced that a global pharmaceutical and biotechnology leader has successfully expanded its use of the ...

In this free webinar, learn how cleaning validation inefficiencies silently undermine overall equipment effectiveness (OEE), and how to fix them. Attendees will learn how capabilities like part-level ...

As recent COVID-19 vaccine facility citations make clear, failure to meet cleaning and sanitization requirements puts patients, facilities, and operators at risk. Keeping pharmaceutical facilities ...

DUBLIN--(BUSINESS WIRE)--The "Regulatory Requirements and Principles for Cleaning Validation" conference has been added to Research and Markets' offering. This two day course will cover practical ...

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

DUBLIN--(BUSINESS WIRE)--Research and Markets has announced the addition of the "Regulatory Requirements and Principles for Cleaning Validation" conference to their offering. This 2 day course will ...

SANTA CLARA, Calif., March 26, 2025--(BUSINESS WIRE)--ValGenesis, Inc., the market leader in digital validation lifecycle management solutions, announced that a global pharmaceutical and biotechnology ...