Advance Research Center LLC

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FAQ

How To Help?How To Help?How To Help?

Frequently Asked
Questions

What is the purpose of the study?


Why do researchers believe the new treatment being tested may be effective?
Has it been tested before?
How do the possible risks, side effects, and benefits in the study compare with my current treatment?
How might this trial affect my daily life?
How long will the trial last?
Who will be in charge of my care?

Inpatient Guidelines Patient Guidelines for Inpatient Trials

It is our pleasure to welcome you to one of our inpatient sites. We are pleased to have you participate in one of our Clinical Research trials. We have taken the time to prepare for you a list of items to consider ensuring that your stay with us is as efficient, comfortable, and as pleasant as possible. Please bring with you the following to your first appointment:

Copies of your medical records.
A complete list of all the medications you are taking, and how you take them. You may bring the actual medicine bottles, If that is easier.
Reading glasses, if necessary.

Please make sure to limit the number of items that you bring with you for your inpatient stay at one of our sites.

Outpatient Guidelines Patient Guidelines for Outpatient Trials

It is our pleasure to welcome you to one of our outpatient sites. We are pleased to have you participate in one of our Clinical Research trials. We have taken the time to prepare for you a list of items to consider assuring that your experience with us is as efficient, comfortable, and as pleasant as possible. Please bring the following with you to your first appointment:

Copies of your medical records.
A complete list of all the medications you are taking, and how you take them. You may bring the actual bottles if that is easier.
Reading glasses, if necessary.

Thank you for considering participation in one of our outpatient studies.

Privacy Policy Let’s protect both of us

Privacy Policy Statement

ARC for Clinical Research’s Privacy Policy is designed to protect patients who have volunteered to participate in a clinical trial. ARC enacts the HIPAA Policy Act in order to ensure the protection of patients’ rights. The HIPAA Act has included a series of conditions that require the Department of Health and Human Services (HHS) to adopt national standards for electronic health care transactions. ARC accumulates patients’ personal information, i.e., name, address, phone number, or E-mail address, only when this evidence has been voluntarily supplied.

Any time that there is any information exchanged between a patient and this website, whether that information is channeled through questionnaires or forms on this site or via regular E-mail, will be monitored Internet security measures, i.e., firewalls, in order to preserve high standards of patient confidentiality.

The information posted on this website is not intended to interfere with those relationships between patient and his or her personal physician. Information concerning diagnosis, condition, treatment, or evaluation is meant solely for educational purposes.

Accumulation of Evidence

ARC for Clinical Research accumulates patients’ personal information, i.e. name, address, phone number, or E-mail address, only when this evidence has been voluntarily supplied. If a visitor wishes to keep his/her information private, or if he/she has concerns about maintaining the confidentiality of specific pieces of information within our system, then it is suggested that the visit refrain from providing this information. The information provided to us will only be used for purposes indicated in the type of form that the visitor fills out and/or questions that the visitor answers.

Use of Information

ARC limits access to information only to those individuals who are responsible for responding to visitors’ specific requests. ARC is required to reasonably safeguard protected health information (PHI) – including oral information – from any intentional or unintentional use or disclosure that is in violation of the Privacy rule. ARC will attempt to contact visitors who have voluntarily submitted their information to the website’s database using the preferred method of contact that has been selected.

The information that is typically requested within the questionnaire is the city, state, and zip code of any visitor who requests information about participating in a ARC. ARC requests this information in order to match visitors up with a clinical research site that is within the area. This information is also stored in our database in case there any future studies arise for which those visitors may be qualified. ARC will be able to contact visitors in the future should this situation occur.

This website is meant to act as a setting for collected information for those purposes specified by visitors. ARC has no control over the quality, truth, or accuracy of information supplied by visitors; it is not the responsibility of ARC to determine the validity of the submitted evidence. Visitors to the website are personally responsible for the information that they voluntarily submit to ARC.

Only the visitor may provide us with the authorization to use the information supplied for the purposes for which it was provided. ARC is under no obligation to use or retain any of the information a visitor submits and may choose to delete such information. The visitor must specify if he or she wants that information to be stored within our database for a certain period of time. If circumstances suggest reasons for severing ties with a certain patient, ARC also has the right to suspend or terminate a visitor’s right to submit information to the website.

ARC updates this website on a monthly basis, and may decide to change parts of the Privacy Policy at certain times. Visitors will receive notice of these changes based on the postings on this website.

Visitor Options

If visitors have submitted a contact form or prescreen form, and wish it to be deleted from or saved within this database, please email info@advanceresearchcenter.com. If possible please specify what contact form was filled out and when it was submitted so the proper information can be removed from the appropriate database.

Patients may also send their inquiries regarding clinical trials info@advanceresearchcenter.com

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