Raptim Research Private Limited (formerly known as Raptim Research Limited), is a global independent and internationally accredited Contract Research Organization (CRO), established in 2005 with state-of-the-art clinical research facilities in Mumbai and Gandhinagar (India). We apply innovative tools and processes to our clinical development and support end-to-end services under the Clinical Research domain for all Global Pharmaceutical companies. With our experience and enhanced capabilities, we are in a unique position to assist our Sponsors with unparalleled support and provide them a single, global research network.

1. Some Of The New Technologies
That We Are Working With Are
Raptim Research
www.raptimresearch.com/

2. Clinical Trial Management System (CTMS)
Raptim Research
CTMS is a suite of eClinical tools that, are most effective
on following part:
• Project Plan & Track
• Monitoring Planning & Management
• Contract & Milestone Tracking (Sites & Teams)
• Subject Visit Tracking
• Document Management

3. Electronic Trial Master File (eTMF)
Raptim Research
An eTMF is a Trial Master File in electronic format. It is a way of
electronic capturing, managing, sharing and storing essential
documents and content related to clinical trials. Global, real-time
access, the ability to manage study files and document workflows,
collaborate, and maintain all essential metadata and audit trails are a
few reasons why using an electronic format is preferred by regulatory
agencies and also by organisations.
www.raptimresearch.com/

4. Remote Source Data Verification (rSDV)
Raptim Research
www.raptimresearch.com/
With the challenges of Covid-19 pandemic, regulatory authorities are
suggesting remote approaches to conducting studies and more and more
trials are looking forward to utilising remote technologies. By conducting
SDV remotely, we go one more step ahead with a risk-based approach in
clinical trials. With RBM techniques it helps to improve the data integrity.
With this tool, it is possible for multiple site’s source data to be checked
at a single centralization location without physically visiting a particular
site.

5. CRED-Bio
Raptim Research
www.raptimresearch.com/
Advantages:
• Complete tracking of the volunteer database and records
• Convenient sample management as data samples come in a neat
format
• One central place to review study-related data
• No manual intervention needed, minimizes the chance of error
• Easier movement tracking
• All acceptance is handled by the system
• Eliminates the chances of backup skip or deviation

6. Raptim Research
Contact Us-
www.raptimresearch.com/
contact@raptimresearch.com

7. Raptim Research
Thank
You!
www.raptimresearch.com/