Efficient collecting, transferring, and managing of data during a clinical trial is crucial and helps advance the drug development process in all clinical research organization.

1. Data Management In Clinical Research

2. 
Introduction to CDM
From a business point of view, drug developers want to ensure that
the data delivered to regulatory bodies is dependable; from an
ethical perspective, clinical data inform treatment decisions and
ultimately affect patient's health. Due to both of the reasons,
clinical data quality and integrity are crucial. Though it seems that
data management only happens after the data are collected, the
process begins before the study protocol is finalized. Since CDM
is best viewed as a process that is very important throughout the
entire clinical study, it is important to involve the CDM team from
the beginning, starting with protocol development.

3. 
CDM PROCESS
A Case Report Form CRF is designed by the CDM team for data
collection from protocol-specific activities. The CRF may exist in
either a paper version or as electronic data capture. The CRF will
be annotated with coded terms where the data collected for each
question is to be stored in the database.

4. 
CONCLUSION
Careful clinical data management is very important to the integrity
of a clinical research. Involving the CDM team early on ensures
that a solid data management plan is set forth from the start.
In the race of many institutes of clinical research, CRB Tech
Solutions has it own name. Its very popular in offering the best
Clinical Training programs.
Clinical Research review by CRB Solutions will help you guide in
considering and taking up a career in this field.

5. Thank You !

6. Thank You !