Successful Strategies
SSLS is a client solution consulting firm founded in 2020, dedicated to revolutionizing the life sciences industry through strategic guidance, process optimization, and innovative solutions. Led by CEO Tamika Jackson, SSLS focuses on regulatory information management, clinical study documentation, diversity, equity, & inclusion (DE&I), and research & development (R&D) systems exchange. The company emphasizes process-centered solutions to foster inclusivity, efficiency, and impactful clinical trials, aiming to become a trusted leader in the field.
Industries
Nr. of Employees
small (1-50)
Successful Strategies
Rancho Cucamonga, California, United States, North America
Services
Consulting and implementation services to centralize regulatory data and documentation, provide controlled document management, regulatory publishing, and e-submission transmission capabilities.
End-to-end Trial Master File services including education, setup, process implementation, QC, scanning, filing, and delivery of TMF mock audit reports to support inspection readiness.
Services to align people, processes, and technology across R&D platforms, including business requirements implementation, technology integration, process optimization, and data management.
Comprehensive DE&I services for clinical trials covering education, strategy development, operational administration, execution, data collection and analysis, and post-study evaluation.
Consulting and implementation services to centralize regulatory data and documentation, provide controlled document management, regulatory publishing, and e-submission transmission capabilities.
End-to-end Trial Master File services including education, setup, process implementation, QC, scanning, filing, and delivery of TMF mock audit reports to support inspection readiness.
Services to align people, processes, and technology across R&D platforms, including business requirements implementation, technology integration, process optimization, and data management.
Comprehensive DE&I services for clinical trials covering education, strategy development, operational administration, execution, data collection and analysis, and post-study evaluation.
Expertise Areas
- Regulatory information management
- Regulatory submissions strategy and publishing
- Trial Master File management and inspection readiness
- R&D systems implementation and integration
Key Technologies
- Document management systems (DMS)
- E‑submission transmission platforms
- Regulatory publishing tools
- R&D systems integration and interoperability