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Drug Management System (Synopsis)

The document discusses a drug research and development management system for an organization called Human Life Innovators Pvt. Limited. Currently, the organization manages drug trials, participant information, and research data manually, which is inefficient and prone to errors. The proposed new system will automate these processes by integrating all data into a centralized SQL Server 2000 database for easier retrieval and coordination. This will allow administrators to more easily collect and access consistent information, and provide instant drug details, trial histories, and research status. The system is being developed using ASP.NET and will improve management of clinical drug research and development.

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sanjaykumarguptaa
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789 views10 pages

Drug Management System (Synopsis)

The document discusses a drug research and development management system for an organization called Human Life Innovators Pvt. Limited. Currently, the organization manages drug trials, participant information, and research data manually, which is inefficient and prone to errors. The proposed new system will automate these processes by integrating all data into a centralized SQL Server 2000 database for easier retrieval and coordination. This will allow administrators to more easily collect and access consistent information, and provide instant drug details, trial histories, and research status. The system is being developed using ASP.NET and will improve management of clinical drug research and development.

Uploaded by

sanjaykumarguptaa
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOC, PDF, TXT or read online on Scribd
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Drug

Management
System

Drug Audition & Research Management is a system that practically


concentrates on the associative standards of the Medical diagnosis and
Research Developments environments. The major problem in Drugs and
pharmaceuticals industry is to design or invert a new Bio-molecular
combination of a chemical. The new Bio molecular combination should have
the ability in training its roots towards the ailment that exists in the body
and fight against that ailment. In the initial stages while the drug is under
the preparatory stages of experiment, it is combinationally checked on
some of the living organisms, which belong to the species of mammals.
Once the drug trial experiments come to a proper status on these animals to
have precision check and reliability standards, they are once again checked
upon the human beings who are physically associated to such problems.
The individuals who are suffering through proper ailments are recognized
and they are requested to participate in the Drug trials voluntarily. The
participation of the individuals is governed through the Byelaws and legal
procedures that exist under the human and civilian rights of the constitution
governed by the European Union. The application increases in its size
through the database, as the research activity increases within the
organization. At a specific time the search of required information takes a
great lot of time the search of required information takes a great lot of time
and costs the organization both in time and money.
The present application concentrates on the relative information that has
been stored at the level of the organization while the system is under the
process of execution. To keep the latency of the system at the lowest profile
the system manages all the information in MS SQL Server 2000 database, to
keep at least of the database standards that are existing at the industrial
level. The application has been developed using the .NET technologies to
keep pace with the present trends of the industrial requirements. The
different standards of the .NET technology have been adapted to Cater to
the standards like Intranet based standards and browser specific user
interfaces. The ADO.NET database connectivity has been exploited for the
database interactive standards.

The entire project has been develped keeping in view of the Distributed
client server computing technology in mind.The specification have been

normalized upto 3NF to eliminate all the anomalies that may arise due to
the database transactions that are executed by the actual administration
and users.The user interfaces are browser specific to give distributed
accessability for the overall system.The internal database has beeb selected
as MS SQL Server 2000. The MS SQL Server 2000 was a

choice as it

provides the constructs of high level reliabiity and security.The total front
end was dominated using HTML standards applied with the dynamism of
ASP.NET. Thecommunicatin client was designed using C#.NET. At all proper
levels high care was taken to check that the system manages the date
consistency with proper business validations.The database connectivity was
planned using the ADO.NET DataBase Connectivity. The authorization was
cross checked at all stages.The user level accessabiity has been restricted
into two zones the administrative and the normal user zone.
About the Organization
The

Human Life Innovators Pvt. Limited is a Drug Research and

Development Foundation, which has its roots of existence in the Bio Medical
Drugs Research for 20 years. The organization has a vast database that has
been collected from the association of the system for all those years. The
present slystem is flooded with huge database and it is an unmanageable
task for the existing staff in retrieving the applicable and required data
within the limited time frame. The system has a huge resource of drugs that
are practically made to participate in the trials. Each drug can have various
reaction agents, that may be necessary under some special circumstances
for the overall chemical reaction to be analyzed and scheduled. The system
has very specific processed information that gets revealed upon the
execution of the reactions and Drug trial participations. The overall scenario
of the Drug and its effectiveness of usage has to be recorded at every stage
any mis-confusion or discrepancy is the manual processcan always create a
havoc under the normalo operational standards of the system. To keep the
standards of precision the system needs. The accumulated information
should be collected and integrated at all different levels of the organization
for smooth functioning and coordination of the system. The system needs
proper handling of the investigation and the Drug trial participants along
with

the

clinical

condition

upon

which

they are

being

treated

or

experimented. The actual system under the manual process needs a huge
amount of manpower in managing and maintaining the information, any

miscoordination among the existing users within the working system can
cause overall disturbance within the date management standards.

Manual Process
First Phase
Informatio
n about
The New
Drug

Identify
the
associated Drug
Reaction agents

Register the
Reference of
Drug along with
the usage
conditions

Search the Ledger


of Reaction agents

Identify the Drug

Prepare a reference
to
the
required
Drug

usage conditions

Second Phase

Make
a
Registration
for
new Drug Trial

Checking the
outcome make
any
recommendati
ons
as
necessary

Register the Drug


in
one
of
the
existing
masters
ledgers.

Register
the
information of the
trial outcomes as
and when it is
applied for testing

Search the
listed Drugs
that are
authorized for
trials

Identify the
required individual
on whom the trial
has to be applied

Why the New system


The development of the new system contains the following activites, which
try to automate the entire process keeping in view of the database
integration approach.

1. The administrators have greater accessibility in collecting the


consistent information that is very much necessary for the system to
exist and coordinate.
2. The system at any point of time can provide the details of all the
drugs that exist within the system along with their reaction agents
combination.
3. The system can provide the generic details of all the allergies and its
associated drugs that can be applied upon it, with a click of the
mouse.
4. The system can provide instantaneous information related to the
drugs and their usage conditions along with the special instruction if
any.
5. The system with respect to the necessities can identify all the history
details of the real participants along with their outcome of the results.
6. The system with respect to the necessities can identify all the history
details of the trial participants along with their outcome of the results.
7. The system with respect to the necessities can provide the status of
research and development process that is under schedule within the
organization currently.
8. With proper storage of the data in a relational environment the
system can aggregate itself to cater to the standards of providing a
clear and easy path for future research standards that may arise due
to organizational policies.

SOFTWARE REQUIREMENTS
The software used in this project is:
Operating System : Windows 2000.
Software

: ASP. Net.

Data Base

: SQL Server 2000

HARDWARE REQUIREMENTS
The hardware used in this project is:
RAM

: 256 MB.

Processor

: P-IV Processor.

Hard Disk : 20 GB
Memory

:32 MB.

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