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Learn how to coordinate the installation qualification (IQ) process with the vendor, the user, and the quality assurance (QA) team for your equipment qualification…
Learn how to use risk assessment and continuous improvement to optimize your requalification process for laboratory equipment and ensure data integrity and quality.
Learn how to overcome common challenges in OQ of your equipment with practical solutions for criteria, tests, results, changes, integration, and maintenance.
Learn how to perform gap analysis and remediation for existing or legacy equipment that may not have clear validation acceptance criteria (VAC).
Learn how to use tools like Excel, Minitab, Word, or SQL Server for requalification data analysis and reporting. Find out how to comply, ensure quality, and enhance…
Learn how to evaluate and select the best change control software for your equipment qualification needs. Follow these tips to compare, test, and decide on the…
Learn what are the key elements of a design qualification (DQ) protocol and report, and how they can help you achieve compliance and quality in your equipment…
Learn how to document the design qualification (DQ) results and deviations in a clear and concise way, using examples and templates. DQ verifies your system or…
Learn how to handle equipment qualification changes in a multi-site or global context with best practices and challenges for change control.
Learn how to incorporate change control and preventive maintenance into your requalification plan for your equipment. Find out how to evaluate, document, and…
Learn how to align your equipment qualification process with your quality management system and improve your equipment performance and compliance.
Learn about the most common and useful sampling techniques for equipment cleaning verification in the pharmaceutical industry, such as swab, rinse, coupon, and…
Learn how to prepare, execute, and document the performance qualification (PQ) protocol and report for your equipment, and how to verify and validate them.