Vendor needs to provide patient safety monitoring solution.– Supporting and monitoring the quality and reliability of Protocol–specified laboratory test results.– Supporting and monitoring compliance with good clinical laboratory practice (GCLP) standards.– Providing Labs with various means of assistance, guidance and training to improve the quality of laboratory.– Hosting and maintaining the existing electronic data management system.– Review audit reports and identify findings that indicate lack of compliance with GCLP.– Review documents received from Labs in support of addressing audit findings.– Provide technical support and guidance to Labs for proper conduct of method validations or verifications, as needed, to ensure compliance with regulatory requirements.– The application used shall be web–based and easy to navigate by various characteristics/parameters (e.g., by country, city, name of lab and document type). The web–based application and other applicable internet and intranet information services. The contract period will be for one year. All the questions must be submitted no later than February 09, 2026.