• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • Clinical Trial Listings
    • What are Clinical Trials?
    • Become a Clinical Trial Volunteer
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Market Research
    • Benchmark Reports
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • White Papers
    • SOPs
  • White Papers
  • Clinical Trial Listings
  • Advertise
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » CSSi LifeSciences introduces SmartStudy Design and Feasibility

CSSi LifeSciences introduces SmartStudy Design and Feasibility

February 4, 2015
CenterWatch Staff

CSSi LifeSciences, a Glen Burnie, Md.-based provider of fully integrated solutions that span the lifecycle of a new drug or device, has launched its newest product offering in its portfolio of services—SmartStudy Design and Feasibility. CSSi LifeSciences is a partner company of global patient recruitment solutions provider CSSi.

CSSi LifeSciences recognizes patient-centricity in clinical trials needs to be at the forefront of clinical development, and some of the biggest challenges in delivering a successful clinical study are identifying, measuring and understanding its real-world patient population and the implications for the study's design and product marketing claims.

Emerging biopharma companies often have deep scientific in-house expertise but limited clinical trial design experience for regulatory approval. CSSi LifeSciences has developed models that reduce time to market and decrease development costs, incorporating protocol optimization and feasibility, study planning and design, and patient recruitment and site selection in SmartStudy.

    Upcoming Events

    • 05Dec

      Thriving in Clinical Research – Overcoming Common Challenges as a Site: Part 3 – Site Resourcing

    • 14Apr

      MAGI 2024: The Clinical Research Conference

    Featured Products

    • Surviving an FDA GCP Inspection

      Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs

    • Best Practices for Clinical Trial Site Management

      Best Practices for Clinical Trial Site Management

    Featured Stories

    • Jonathan Seltzer

      Thought Leadership: Remote Patient Monitoring Gives New View of Safety in Cardiac Clinical Trials

    • Quality_Compass-360x240.png

      Ask the Experts: Applying Quality by Design to Protocols

    • Obesity Treatment Patient

      Clinical Trials Need Greater Representation of Obese Patients, Experts Say

    • Modernize-360x240.png

      FDA IT Modernization Plan Prioritizes Data-Sharing, AI, Collaboration and More

    Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

    The information you need to adapt your monitoring plan to changing times.

    Learn More Here
    • About Us
    • Contact Us
    • Privacy Policy
    • Do Not Sell or Share My Data

    Footer Logo

    300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

    Phone 703.538.7600 – Toll free 888.838.5578

    Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing