Clinical Trial Management Service

1
Resolve Medicode
Clinical Trial Management Services
Creating Future Oriented Solutions
2
About Us

• We partner with you to apply time-tested
  strategies and next generation solutions.
• We help improve health outcomes, drive innovation
  and enhance efficiencies.

3
Clinical Trial Management Services

• If you are looking for an expert partner to
  manage your clinical trial, we are at your
  service.
• As a full-service CRO we support you on all
  levels and in, every step of your clinical
  research project.

4
CTMS offers investigators, collaborators and
sponsors several benefits, including
Simplify-The powerful site and data management
tools, including medidata rave, automate many of
the functions for setting up and managing
multi-site clinical trials and complex studies.
5
Streamline-Increased efficiency in data
collection, lock down (validation) and analysis
shortens the time from study completion to
reporting and publication. CTMS tools reduce the
administrative burden for investigators and study
team members, creating additional capacity for
research projects.
6
Standardize-When completely implemented, CTMS
will integrate seamlessly with other Mayo Clinic
research and IT systems, and facilitate
collaboration with industry sponsors, foundations
and federal funding agencies.
7
Project Management

• When we lead your project, our main concern is to
  release you from any stress related to the
  project management.
• We always keep a strict eye on quality, budget,
  and timeline.
• We are there to make sure, your clinical trial
  runs smoothly.

8
What Your Dedicated Project Team Will Do for You?

• Plan and execute critical milestones for each
  study.
• Provide excellent customer service and proactive
  communication.
• Identify efficiencies and processes to improve
  your data quality.

9
Site Management

• We properly review the subjects safety and the
  sites adherence to regulations.
• Maintain regular and proactive communication with
  all parties, at every stage from start-up to
  close-out.
• This collaboration increases the quality of your
  data and makes sure your trials run efficiently.

10
Site Selection

• The right site meets many needs.
• It must fit the sponsors needs, but also the
  study requirements for start-up activities.
• Right site is a highly productive site in a
  suitable geographical location, that can
  efficiently achieve your goals.

11
Eligibility

• Candidates who have a degree in - life science or
  bio-sciences, medicine, pharmacy and
  pharmaceutical sciences, nursing or allied health
  are eligible.

12
Reach us
https//medi-code.in info_at_medi-code.in 91 81484
52460 91 75400 52460