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  • *NEW INFO* Prism Text

      Prism is excited to announce we have started PRISM TEXT! This texting feature will be a convenient way for the Recruitment Department to TEXT you about upcoming studies. 

      You will be receiving text message from us if you are qualified for a study.

      You are considered OPT-IN unless you tell us to remove you (OPT OUT).

      The texting system is through our secure online database and will not compromise  your phone number. 

       

      Please let us know if you have any questions! 

      Recruitment

      Lindsay 651-368-3360

      Dayna 651-724-5047

      Jenna 651-724-0500

      Andy 651-332-1810

    • Register with Our Database

      Registration form here.

        Get started on the volunteer process by registering your basic information with our database. This information is provided to help us determine your eligibility for current and future studies.

        If you have registered with Prism in the past, please call Dayna 651-724-5047 to update your profile or learn about available studies.

        Find the registration form here

         Unfortunately at this time, Prism can not allow volunteers who live over 200 miles away to participate in research studies. If you live out of state or over 200 miles away please call Geoff at 651-641-2911 with questions. 

        We will not share or sell this info with any third party.

        Thanks for your interest!

      • Upcoming Studies

         

         

           Prism has a variety of upcoming studies to participate in: 

          • Inpatient and Outpatient studies for healthy males and females; Age 18-55 years old
          • Liver Impairment 
          • Kidney Impairment 

          To be put on the call list and receive more information, when available, please contact Dayna at daynas@prismresearchinc.com or Lindsay at lindsayd@prismresearchinc.com.

        • Diagnosed with Liver Impairment?

            Prism Research has upcoming studies for individuals diagnosed with liver impairment.  These studies will help determine how an investigational drug is broken down and removed from the body in volunteers with various degrees of liver impairment when compared to volunteers with normal liver function.

             If you or someone you know has been diagnosed with liver impairment and are interested in being considered for these studies, please contact Dayna at 651-724-5047 or register with our database and we will call you. Financial compensation for study participation ranges from $400-$3500.

            Please contact Dayna at 651-724-5047 or daynas@prismresearchinc.com

             

          • Diagnosed with Kidney Impairment?

              Prism Research has upcoming studies for individuals diagnosed with kidney impairment.  These studies will help determine how an investigational drug is broken down and removed from the body in volunteers with various degrees of kidney impairment when compared to volunteers with normal kidney function.

               If you or someone you know has been diagnosed with kidney impairment and are interested in being considered for these studies, please contact Lindsay at 651-368-3360 or register with our database and we will call you. Financial compensation for study participation ranges from $400-$3500.

              Please contact Lindsay at 651-368-3360 or lindsayd@prismresearchinc.com

            • Refer Your Friends & Family to Participate

                Simply help us get the word out about Prism Clinical Research and we’ll give you $100 for every friend you refer that completes a study.

                It’s that easy! Make money with each referral, and there’s no limit to how many friends you can refer!

                Rules:

                • Subject must qualify for a study.
                • Subject may not be referred more than one time.
                • Subjects eligible for Referral: (1) Must not be in Prism Clinical Research database; (2) Must not have participated in any prior study at Prism.
                • In the event that a subject is referred by multiple people, the first person who referred will receive payment.
                • Eligibility will be determined by Prism. Prism reserves the right to revise or eliminate this program at any time without notice.

                 

                 

              • Liver Impairment: Clinical Research Study 1817

                  LIVER IMPAIRMENT STUDY

                  CLINICAL RESEARCH STUDY: 1817

                  PRISM CLINICAL RESEARCH

                  PURPOSE:

                  • To determine how the investigational drug is absorbed, broken down, and removed from the body in volunteers with abnormal liver function compared to volunteers with normal liver function.

                   

                  GENERAL STUDY REQUIREMENTS:

                  • Men and women between the ages of 18 and 80 years old.
                  • Liver Impairment volunteers: must have mild/moderate/severe liver impairment due to diagnosed liver disease.
                  • Healthy volunteers: must be healthy; not being evaluated or treated for any medical conditions.

                   

                  STUDY DURATION:

                  • 1 In-Clinic Stay: Lasting 8 nights/ 9 days
                  • Clinic Visits: 1(screening)
                  • Total Study Duration is Approximately 39 days, including screening

                   

                  METHOD OF ADMINISTRATION:

                  • Oral Administration

                   

                  STUDY COMPENSATION:

                  • Compensation for Study Participation may be provided for time and travel up to $2620.00

                   

                  RECRUITMENT CONTACT:

                • Kidney Impairment: Clinical Research Study 1907

                    Renal Impairment Study

                    Clinical RESEARCH study: 1907

                     

                    PRISM RESEARCH

                     

                    Purpose:

                    • To evaluate the safety and tolerability of an investigational drug being developed for  a type of liver disease

                     

                    GENERAL STUDY REQUIREMENTS:

                    • Men and women between the ages of 18-70 with a BMI between 18-38
                    • Must be a nonsmoker
                    • Medical conditions and medications must be stable in the opinion of the study doctor.

                     

                    STUDY DURATION:

                    • In Clinic Stay: 11 nights/12 days
                    • Return Clinic Visits: 4 including screening
                    • Total study duration is up to 49 days

                     

                    METHOD OF ADMINISTRATION:

                    • Oral Dose

                     

                    STUDY COMPENSATION:

                    • Compensation up to $3980.00for Study Participation Time

                     

                    RECRUITMENT CONTACT:

                  • Kidney Impairment: Clinical Research Study 1910

                      Renal Impairment Study

                      Clinical RESEARCH study: 1910

                       

                      PRISM CLINICAL RESEARCH 

                       

                       

                       

                      Purpose: 

                      •  To evaluate the safety and tolerability of an investigational drug in individuals with renal impairment compared to individuals without renal impairment.

                       

                      GENERAL STUDY REQUIREMENTS:   

                      •  Men and Women, between the ages of 18 to 75 with a BMI between 17.5-40kg/m2.
                      •  Medical conditions and medications must be stable in the opinion of the study doctor.

                       

                      STUDY DURATION: 

                      •  Clinic Visits: 2 (Including screening)
                      •  In Clinic Stay: 11 nights/12 days
                      •  Follow-Up Visit: via phone
                      •  Total study duration may be up to 74 days

                       

                      METHOD OF ADMINISTRATION:

                      •  Oral Administration

                       

                      STUDY COMPENSATION: 

                      •  Compensation for Study Participation Time Up To: $3,885.00

                       

                      RECRUITMENT CONTACT:

                       

                       


                       [RK1]Please update the version date when the revised version is sent

                       [RK2]I believe the draft budget has a total of $3,980. Please confirm which is correct. The ICD also has $3885, so maybe the budget needs to be updated. NOTE: The budget has 2 screening visits included at $95 each.

                    • Liver Impairment: Clinical Research Study 1913

                        Liver Impairment Study

                        Clinical RESEARCH study: 1913

                         

                        PRISM RESEARCH

                         

                        Purpose:

                        • To evaluate the safety and tolerability of an investigational drug being developed for treatment of certain types of cancer in healthy volunteers and volunteers who have been diagnosed with different levels of liver impairment.

                         

                        GENERAL STUDY REQUIREMENTS:

                        • Men and women between the ages of 18-75 with a BMI between 18-40
                        • Liver impairment volunteers: must have mild/moderate/severe liver impairment documented by medical history
                        • Healthy Match volunteers: must be healthy; not being evaluated or treated for any medical conditions

                         

                        STUDY DURATION:

                        • In Clinic Stay: 9 days/8 nights
                        • Return Clinic Visits: 2 including screening
                        • Total study duration is up to 43 (including screening)

                         

                        METHOD OF ADMINISTRATION:

                        • Oral Dose

                         

                        STUDY COMPENSATION:

                        • Compensation for Study Participation Time Up To: $2740.00

                         

                        RECRUITMENT CONTACT:

                      • Sample Trial Available for 70+ year olds: Study 1914

                          BLOOD SAMPLE STUDY

                          Clinical RESEARCH study: 1914

                           

                          PRISM RESEARCH

                            

                          Purpose:

                          • To collect blood specimens and clinical data from individuals who have not been diagnosed with heart failure.

                           

                          GENERAL STUDY REQUIREMENTS:

                          • Generally healthy
                          • Medication will be approved on a case by case basis

                           

                          STUDY DURATION:

                          • 1 outpatient visit lasting approximately 3 hours

                           

                          METHOD OF ADMINISTRATION:

                          • This is a sample collection study; no study drug will be administered.

                           

                          STUDY COMPENSATION:

                          •  Compensation for Study Participation Time Up To: $85.00

                           

                          RECRUITMENT CONTACT:

                           

                        • Connect With Prism Research on Social Media

                             

                            Have you LIKED Prism Clinical Research on Facebook?

                            Have you TAGGED Prism Clinical Research on Twitter?

                            Have you FOLLOWED Prism Clinical Research on Instagram?

                             

                            Use the links below:↓

                            https://www.facebook.com/PrismResearch/

                            https://twitter.com/ResearchPrism

                            https://www.instagram.com/prismclinical_research/?hl=en

                             

                          Where hope, science & understanding meet.

                          From the aspirin on the shelves of your local drugstore, to the insulin prescribed by a doctor, to the pacemaker keeping someone’s heart on track – all have been subject to clinical trials, and integral part of the Food and Drug Administration (FDA) approval process.

                          A critical step in an important process

                          Drugs and medical devices undergo years of laboratory testing before they reach the clinical trial phase. Researchers must acquire approval from the FDA for approval to continue research and testing in humans. Clinical trials are essential to measure the efficacy and safety of drugs before they are available for widespread use.

                          Changing lives, every day.

                          The impact of clinical trials are seen in our everyday lives, in the confidence with which we can take over-the-counter drugs – or in the life-saving benefits of a breakthrough medication for a victim of Leukemia.

                          Public Health and Safety

                          Prior to the development of the FDA’s rigorous and highly regulated method, consumers had to rely upon the anecdotal observation of physicians or spurious claims of pharmacists. In 1906, in order to protect public health and safety, the fledgling FDA passed the first regulatory drug act – the Pure Food and Drug Act.

                          In 1938, the enactment of the U.S. Food, Drug, and Cosmetic Act subjected new drugs to pre-market safety evaluation for the first time, thus enabling FDA regulators to review both pre-clinical and clinical test results, giving them the authority to block the marketing of a new drug formally or delay it by requiring additional data.

                          Alongside the evolving standards of drug regulations, closer regulation of the clinical trial process. The resulting process today is designed to protect the safety of study participants, promote the development of lifesaving drugs, and keep public health and safety at the center of medical advancement. In the century since the first drug act, the research and medical community in cooperation with the FDA, have developed the foremost institutional authority for conducting and evaluating controlled clinical drug trials.

                          Doing the right thing

                          Know that you’ve done your part to help make important medications available to those who need them. If you have a friend or family member who relies on a medication to treat a chronic disease or illness, they have benefited from the work of a clinical trial, and a volunteer like you who gave their time and effort to aid in the approval process.

                          Fair compensation for your time

                          You’ll be compensated based on the time you spend as a study participant.

                          Medical exam & monitoring

                          As a study participant, you’ll likely receive a full medical examination and testing for a variety of conditions. In some cases volunteers might have access to treatments or medicines before they are available to the general population.

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                          Prism Clinical Research provides, FDA approved, investigational pharmaceutical and medical device testing services on behalf of drug and device manufacturers, academic and private physicians as well as other researchers across Minnesota.

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                          At Prism, we are committed to the advancement of medical knowledge and the health of our community. We have been conducting Phase I clinical trials since 2005, helping many important drugs reach FDA approval. Prism is a locally owned and operated, independent facility in the heart of the Minneapolis/St. Paul metropolitan area. 

                          Whether you are here because you are interested in participating in a clinical trial, or you’re searching for a trusted partner to conduct a study on your behalf, our hope is that you find the information you need and the confidence to take the next step. 

                          With your help, we can make a difference.


                          Learn what Prism Volunteers are saying:

                          Volunteer Large 13

                          "I am VERY pleased with Prism Research. I enjoy the studies and the staff is always friendly and they all make you feel as comfortable as possible. The study compensation program is very good as well! Thank you."

                          • Capture

                            “Awesome as always!  The staff is great and they are very professional.”

                          • Volunteers 05

                            “Really a great experience!”

                          • Volunteers 06

                            “Staff was courteous and well informed of the nature of the study and all of the requirements that went with it.”

                          • Volunteers 07

                             “Overall my experiences at Prism have been very positive and directly linked to the Staff - their demeanor, humor and professional approach.”


                          Please provide us with your contact information (below) and will get back to you as soon as possible.

                          If you have a general question, check Volunteer FAQ for an answer. If you're unsure of who to contact, please visit the Contact Us page.

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