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Clinical Research Training in Hyderabad


Clinical research is a branch of medical science that determines the safety and effectiveness of medications, devices, diagnostic products and treatment regimens intended for human use. These may be used for prevention, treatment, diagnosis or for relieving symptoms of a disease. Clinical Research is different than clinical practice. In clinical practice, one used established treatments while in clinical research evidence is collected to establish a treatment. – PowerPoint PPT presentation

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Title: Clinical Research Training in Hyderabad

Clinical Research, Clinical Data Management
Clinical ResearchThe National Institutes of
Health NIH explains clinical research as
study administered with human subjects or on
elements of human origin like specimens, tissues,
etc., for which a researcher interacts directly
with human subjects. In vitro studies are not
included in this as they are not linked to a
living individual.
Clinical research comprises of clinical trials,
which are investigations that analyze the
efficacy and safety of medical devices or drugs.
These investigations are carried out in line with
a formal protocol, which categorizes what kind of
patient can participate, what is being measured,
when and how much treatment is given, and the
overall duration of the study.
Clinical Trial PhasesClinical trials advance in
phases, making headway toward use for patient
care after the drug/device has been thoroughly
studied for effectiveness and safety. The stages
of clinical trials, which each new treatment must
pass to be introduced into the market
includeClinical Data Management Training
In phase I, researchers would test a new
drug/treatment in a small group of individuals to
analyse its safety, ascertain a safe dosage
range, and identify the side effects.In phase
II, the drug or treatment is administered to a
larger group of people to analyse if it is
efficacious and to further assess its safety.In
phase III, the drug or treatment is given to
large groups of people to affirm its efficacy,
check up on the side effects, compare it to the
commonly used treatments, and gather information
that will allow the drug or treatment to be used
safely.In phase IV, the studies are done after
the drug or treatment has been distributed to
collect information on the drug's effect in
various populations and any side effects that are
associated with long-term use.
Research Techniques Used in Clinical
ResearchThere are numerous research techniques
used for clinical research such as descriptive,
exploratory, and experimental studies.Clinical
Data Management Training in Hyderabad
Descriptive ResearchDescriptive research makes
surveillance about patients or health-related
conditions. Usually, this investigation includes
a small sample of patients and intensively
studies them to get an idea into the subject of
interest. Some examples of these include,
qualitative research, case-studies, surveys, etc.
Exploratory ResearchExploratory research probes
patients or conditions that have not been widely
studied. Exploratory research looks to explain or
define a problem. Many a times, relationships or
associations are looked for so as to better
understand a disease or disorder. For example, a
study may uncover a link between lifestyle
factors and a particular disease. Examples that
include such are case-control studies, cohort
studies, pilot studies, and historical research.
Experimental ResearchExperimental research
comprises comparing two sets of people. Commonly,
one set of the people receive an intervention or
treatment and the other set of people do not. The
aim of this research is to figure the effect of
the intervention. When randomization is used,
these designs are seen as the "gold standard" in
clinical research as the design permits
researchers to rule out most, and maybe all,
substitutive explanations regarding their
results. An example of this is where a researcher
may contrast a group of patients getting a
placebo drug as against a group getting an
experimental drug. If the two groups are
comparable at the beginning of the study, any
differences at the end of the study like
improvement in the disease/disorder in the
experimental group can be traced to the
experimental drug.
Clinical Data ManagementClinical data
management consists of entry, verification,
validation, and quality control of data that is
collected through the implementation of a
clinical trial.
Advancements in the current biopharmaceutical
field demand that clinical data management (CDM)
is at the forefront, causing change, inspiring
direction, and furnishing objective evidence.
Clinical data management needs to rely on a vast
sphere of skills such as technical, scientific,
project management, information technology (IT),
systems engineering, and interpersonal skills to
handle, drive, and offer valued service in
managing data within the foreseen e-clinical age.
Clinical Data Management (CDM) is a vital stage
in clinical research, which leads to generation
of high-quality, reliable, and statistically good
data from clinical trials. This helps to develop
a forceful step-down in time from drug
development to marketing. The team members of CDM
are dynamically involved in all stages of
clinical trial, from inception to completion.
They should have ample process knowledge that
helps uphold the quality standards of CDM
Many procedures in CDM including Case Report Form
(CRF) designing, CRF annotation, database
designing, data-entry, data validation,
discrepancy management, medical coding, data
extraction, and database locking are assessed for
quality at periodic regular intervals during a
trial. In the current setting, there is an
heightened requirement to improve the CDM
benchmarks to conform to the regulatory
requirements and stay in front of the competition
through faster commercialization of the product.
With the enforcing of regulatory compliant data
management tools, CDM team can conform to these
Additionally, it is becoming compulsory for the
companies to present the data electronically. CDM
professionals should comply to appropriate
expectations and define standards for data
quality and also have the vigor to conform to the
fast changing technology.
The CDM process, like a clinical trial, starts
with the final product in the mind, which means
that the entire procedure is planned in keeping
the deliverable in view. As a clinical trial is
projected to resolve the research question, the
CDM procedure is designed to hand over an
error-free, effectual, and statistically
well-grounded database. To meet this aim, the CDM
procedure begins early, even before the
finalization of the study protocol.
The top 10 pharmacological companies listed in
the Fortune 500 companies earn more than the rest
of the 490 companies listed! Well, that surely
tells the story! The future looks bright and
promising for clinical research and clinical data
management, and it would only seem prudent to
give this career a thought.
18 is one of the leaders in training
people in Clinical Data Management and making
them industry-ready.
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