Clinical Trial Management Service
                     Resolve 
Medicode
Clinical Trial 
Creating Future Oriented Solutions
Management Services
About 
• We paUrtnser with you to apply 
time-tested strategies and next 
generation solutions. 
• We help improve health 
outcomes, drive innovation and 
enhance effi ciencies.
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.
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.  
Streamline-Increased effi ciency 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.
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.
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.
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 effi ciencies and processes to 
improve your data quality.
Site Management
• We properly review the subject’s safety 
and the site’s 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 effi ciently.
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 effi ciently achieve your goals.
Eligibility
• Candidates who have a degree in - life 
science or bio-sciences, medicine, 
pharmacy and pharmaceutical 
sciences, nursing or allied health are 
eligible.
Reach us 
 
https://medi-code.in 
[email protected]
+91 81484 52460
+91 75400 52460