SterlingBio — Value Proposition
SterlingBio is a drug development and research management company with the ability to design complete BioPharma product development strategies, provide input from industry thought leaders, design and author clinical development reports and programs, deliver comprehensive Clinical Research Outsourced (CRO) services and successfully manage the regulatory submission process. Our unique leadership in the electronic trial master file area insures that regulatory documentation receives state-of-the-art automated processing, resulting in higher quality and streamlined submittals.
We provide these services in accordance with either an integrated or a segmented model, depending upon the needs of the customer.
How we work with Clients
Clients work with us either on a fixed-cost contract basis or on an hourly basis. Clients can use our consultants to leverage the efforts of an in-house project team or for a complete outsourced management solution. Either way, our professionals manage projects with a commitment to deliver sterling results.
Unique Value Added Expertise, Technology & Methodology
Why do clients retain SterlingBio? For many of SterlingBio’s clients its the combination of our team’s experience and our use of proven clinical trials methodologies, our technology and our proven processes and that gives them the ability to overcome those obstacles that most often impede the clinical research process. For others its simply the personalized service that we offer and the ability to get the job done.
Our value-added expertise includes:
- Extensive network of proven clinical research associates
- Electronic Regulatory Document Management Solutions incorporating industry best practices (SterlingBio SureTrial)
- Extensive library of clinical trials SOP’s
- Collaborative Project Management software
- Personalized service
- Genitourinary System / STDs
- Infectious Disease
- Pulmonary / Respiratory
- Rheumatology / Musculoskeletal
For more information, contact us today.