We Are Proud To Present The Concierge Approach For Life Sciences

Where the solution is determined by the process.

Finally, a methodology that fits your organization’s needs

Diversified Solutions for Life Sciences (DSFLSS) delivers hands-on regulated content management assessment, guidance, and instruction for every major part of a life sciences company. We focus on R&D document development, clinical trials documentation management, regulatory submissions, and DE&I strategy and implementation services.

A relationship that will enrich your experience.

We are not just publishing a submission, managing clinical study documentation, or implementing a research and development system. We focus on looking across the activities during the product’s lifecycle to ensure data flows freely and efficiently across your organization, using a compliant and consistent standard

DSFLSS- Unparalleled Personalized Strategic Planning

Diversity Action Planning
We are a force that propels a new wave of inclusive thinking in clinical trials, marrying process, passion, and purpose to deliver robust Diversity, Equity, and Inclusion Plans (DEI) strategy and implementation services.
Regulatory Information Management
We provide our clients with a complete solution to plan, manage, publish, transmit, and archive regulatory submissions and agency correspondence throughout the products lifecycle.
Systems Implementation
Our R&D Systems Implementation is designed to align with the vendors implementation strategy in order to provide clients with the complete solution: a brand-new system, process, and our expert project resources.
TMF Management
Our TMF Management Strategy is designed to analyze, prepare, implement, and audit your TMF to ensure you are ready for your organization’s next audit or agency inspection. Wherever you are in your process, our solution fits your needs.

Our Significant Milestones In the Industry

17
R&D Implementations
12
Clinical Projects
7
Countries Supported
325
Published and Maintained Submissions

Tailored to Your Needs

We are not just publishing a submission, managing clinical study documentation, or implementing a research and development system. We focus on looking across the activities during the product’s lifecycle to ensure data flows freely and efficiently across your organization, using a compliant and consistent standard