Life Sciences companies can reduce the likelihood of product approval delays by becoming more knowledgeable about regulatory requirements and the impact to their operations. UL partners with clients to ensure that their quality management systems, technology platforms, people readiness and product submission will meet the rigor of the regulators.
Preparation is essential for any audit because of the escalating complexity and overlap of global quality regulations. Failure to meet audit requirements can severely impact the company, causing delays in product launch. UL partners with companies to develop an inspection infrastructure, processes for hosting and responding to inspections, and education for individuals on how to respond to an inspection.
Companies need to educate their GxP workforce on the latest regulations, so they can apply these requirements into their daily processes and procedures. UL provides educational solutions that enables companies to deliver GxP knowledge across multiple regions consistently and efficiently.