Advisory, development, and strategic planning services provided to companies for business purposes in the life sciences industries; Business consultation services in the life sciences fields featuring: end-to-end GxP ("Good Practice") cloud compliance from implementation through ongoing validation maintenance of new releases; product data integration into a modern Quality Management System (QMS) to create more efficient workflows; clinical collaboration in a GxP compliant environment; Computer Systems Validation (CSV); document management systems; enterprise content management systems; workflow and eSignature approval streamlining; digital transformation strategy and roadmapping and application consolidation, including email, document management, file transfer protocol (FTP) servers and file share drives; merger and acquisition standardization and harmonization; GxP compliance for FDA audits, EU audits, and other regulatory agencies; reducing implementation and validation time; harmonizing and centralizing GxP cloud compliance; cost reduction for managing cloud compliance; new release management for continuous cloud compliance; scalable vendor solutions for establishing compliant IT foundations; vendor audits targeted to current processes, technology, and manufacturing; implementation and validation of GxP compliant changes, including regulatory assessment, creation of validation plans and reports, drafting of user requirements and functional specifications, risk and impact assessment, developing IQ/OQ/PQ protocols and test scripts, developing user and administration SOPs; continuous GxP compliance, including managing new vendor releases, conducting impact assessments, updating validation documents, running automated regression tests, and providing continuous analysis and reporting

Providing educational and informational content and customized training materials and programs in the life science fields through various print and electronic multimedia, including: videos, blogs, articles, webinars, white papers, onsite/offsite remote channels, workshops, hands-on training programs, and other training environments in the life sciences fields, including but not limited to the following subject matter: end-to-end GxP ("Good Practice") cloud compliance from implementation through ongoing validation maintenance of new releases; product data integration into a modern Quality Management System (QMS) to create more efficient workflows; clinical collaboration in a GxP compliant environment; Computer Systems Validation (CSV); document management systems; enterprise content management systems; workflow and eSignature approval streamlining; digital transformation strategy and roadmapping and application consolidation, including email, document management, file transfer protocol (FTP) servers and file share drives; merger and acquisition standardization and harmonization; GxP compliance for FDA audits, EU audits, and other regulatory agencies; reducing implementation and validation time; harmonizing and centralizing GxP cloud compliance; cost reduction for managing cloud compliance; new release management for continuous cloud compliance; scalable vendor solutions for establishing compliant IT foundations; vendor audits targeted to current processes, technology, and manufacturing; implementation and validation of GxP compliant changes, including regulatory assessment, creation of validation plans and reports, drafting of user requirements and functional specifications, risk and impact assessment, developing IQ/OQ/PQ protocols and test scripts, developing user and administration SOPs; continuous GxP compliance, including managing new vendor releases, conducting impact assessments, updating validation documents, running automated regression tests, and providing continuous analysis and reporting