Elite Clinical Research Center

07/25/2024

06/04/2024

If interested call 8108209853

03/25/2020

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06/21/2019

𝐇𝐚𝐯𝐞 𝐲𝐨𝐮 𝐡𝐚𝐝 𝐓𝐲𝐩𝐞 𝟏 𝐃𝐢𝐚𝐛𝐞𝐭𝐞𝐬 (𝐓𝟏𝐃𝐌) 𝐟𝐨𝐫 𝐨𝐯𝐞𝐫 𝐚 𝐲𝐞𝐚𝐫?

𝐇𝐚𝐯𝐞 𝐲𝐨𝐮 𝐛𝐞𝐞𝐧 𝐨𝐧 𝐚 𝐦𝐮𝐥𝐭𝐢𝐩𝐥𝐞 𝐝𝐚𝐢𝐥𝐲 𝐢𝐧𝐬𝐮𝐥𝐢𝐧 𝐫𝐞𝐠𝐢𝐦𝐞𝐧 𝐰𝐢𝐭𝐡 𝐫𝐚𝐩𝐢𝐝 𝐚𝐜𝐭𝐢𝐧𝐠 𝐢𝐧𝐬𝐮𝐥𝐢𝐧 𝐚𝐧𝐝 𝐛𝐚𝐬𝐚𝐥 𝐢𝐧𝐬𝐮𝐥𝐢𝐧 𝐟𝐨𝐫 𝐭𝐡𝐞 𝐩𝐚𝐬𝐭 𝟑 𝐦𝐨𝐧𝐭𝐡𝐬?

𝐈𝐟 𝐲𝐨𝐮 𝐚𝐫𝐞 𝐚𝐭 𝐥𝐞𝐚𝐬𝐭 𝟏𝟖 𝐲𝐞𝐚𝐫𝐬 𝐨𝐥𝐝, 𝐲𝐨𝐮 𝐦𝐚𝐲 𝐪𝐮𝐚𝐥𝐢𝐟𝐲 𝐭𝐨 𝐩𝐚𝐫𝐭𝐢𝐜𝐢𝐩𝐚𝐭𝐞 𝐢𝐧 𝐚 𝐫𝐞𝐬𝐞𝐚𝐫𝐜𝐡 𝐬𝐭𝐮𝐝𝐲 𝐭𝐡𝐚𝐭 𝐜𝐨𝐦𝐩𝐚𝐫𝐞𝐬 𝐚𝐧 𝐢𝐧𝐯𝐞𝐬𝐭𝐢𝐠𝐚𝐭𝐢𝐨𝐧𝐚𝐥 𝐢𝐧𝐬𝐮𝐥𝐢𝐧 𝐰𝐢𝐭𝐡 𝐚𝐧 𝐚𝐥𝐫𝐞𝐚𝐝𝐲-𝐚𝐩𝐩𝐫𝐨𝐯𝐞𝐝 𝐢𝐧𝐬𝐮𝐥𝐢𝐧.

𝐈𝐟 𝐞𝐥𝐢𝐠𝐢𝐛𝐥𝐞, 𝐲𝐨𝐮 𝐰𝐢𝐥𝐥 𝐫𝐞𝐜𝐞𝐢𝐯𝐞 𝐬𝐭𝐮𝐝𝐲-𝐫𝐞𝐥𝐚𝐭𝐞𝐝 𝐦𝐞𝐝𝐢𝐜𝐚𝐥 𝐞𝐱𝐚𝐦𝐬 𝐚𝐧𝐝 𝐥𝐚𝐛𝐬, 𝐝𝐢𝐞𝐭 𝐚𝐧𝐝 𝐞𝐱𝐞𝐫𝐜𝐢𝐬𝐞 𝐜𝐨𝐮𝐧𝐬𝐞𝐥𝐢𝐧𝐠, 𝐝𝐢𝐚𝐛𝐞𝐭𝐞𝐬 𝐭𝐞𝐬𝐭𝐢𝐧𝐠 𝐬𝐮𝐩𝐩𝐥𝐢𝐞𝐬 𝐚𝐧𝐝 𝐬𝐭𝐮𝐝𝐲 𝐦𝐞𝐝𝐢𝐜𝐚𝐭𝐢𝐨𝐧 𝐚𝐭 𝐧𝐨 𝐜𝐨𝐬𝐭. 𝐘𝐨𝐮 𝐦𝐚𝐲 𝐚𝐥𝐬𝐨 𝐛𝐞 𝐜𝐨𝐦𝐩𝐞𝐧𝐬𝐚𝐭𝐞𝐝 𝐟𝐨𝐫 𝐲𝐨𝐮𝐫 𝐭𝐢𝐦𝐞 𝐚𝐧𝐝 𝐭𝐫𝐚𝐯𝐞𝐥.

𝐈𝐟 𝐲𝐨𝐮 𝐰𝐨𝐮𝐥𝐝 𝐥𝐢𝐤𝐞 𝐭𝐨 𝐥𝐞𝐚𝐫𝐧 𝐦𝐨𝐫𝐞, 𝐜𝐚𝐥𝐥 𝐄𝐥𝐢𝐭𝐞 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐑𝐞𝐬𝐞𝐚𝐫𝐜𝐡 𝐚𝐭 𝟖𝟏𝟎-𝟖𝟐𝟎-𝟗𝟖𝟓𝟑 𝐨𝐫 𝐯𝐢𝐬𝐢𝐭 𝐮𝐬 𝐨𝐧𝐥𝐢𝐧𝐞 𝐚𝐭

We do Research Here Elite Clinical Research center is an independent center for conducting clinical trials in a broad array of specialties. Research team of physicians, administrative staff and medical director is highly dedicated and motivated to provide the highest quality clinical research servic...

01/15/2015

Patient Safety is our Top Priority. To be protected you can be assured that:

* The ethical and legal codes that govern a medical practice also apply to clinical trials.
* Every clinical trial in the United States must be approved and monitored by an Institutional Review Board (IRB) to make sure the risks are as low as possible and are worth any potential benefits.

01/15/2015

What is an IRB?

An Institutional Review Board (IRB) is an independent committee of physicians, statisticians, community advocates and others who ensure a clinical trial is ethical and participants’ rights are protected

09/30/2014

How is the safety of the participant protected?
Clinical studies are designed to ensure that volunteers are not put at undue risk. Clinical studies follow a carefully controlled protocol, a study plan which details what researchers will do in the study. As a clinical study progresses, researchers report the results of the study at scientific meetings, to medical journals and to various government agencies. Individual participants’ names remain secret and are never mentioned in any reports.

09/19/2014

What is informed consent?
Participants must sign an "informed consent" document before joining the study indicating they understand that the study is research, and that they can leave the clinical study at any time. The informed consent details the nature of the study, the risks involved, and what may happen to a participant in the study. The informed consent tells participants that they have a right to leave the study at any time.

08/17/2014

What is a protocol?
A protocol is “A document that describes the objectives, design, methodology, statistical considerations, and organization of a clinical trial”
The protocol describes:
• The type of participant
• The schedule of tests
• Procedures
• Medications and dosages
• The duration of the trial
• Definition of the ‘end of the trial’

08/13/2014

Who can participate?
Eligibility Criteria are unique to the particular study. The criteria is based on such factors as age, s*x, gender, health history, previous treatment history, and other medical conditions and basic lifestyle. Before joining a clinical study, a participant must be qualified.