Headline
The clinic works closely with sponsors, study investigators, clinical staff, ethics board, and participants to ensure that studies are conducted efficiently, safely., and ethically. They are involved in various tasks such as recruiting and screening participants, data collection, and managing documentation. Complete, accurate, secure, and timely reporting of data is essential. They function under the direction of experienced investigators to provide participant care and human subject protection, while using professional judgment and sound decision making in the context of the clinical research setting.
These activities contribute to meeting research objectives, safety and comfort needs of participants, and are performed in accordance with all existing regulatory, state and company standards, policies and procedures. Our staff are primarily responsible for the accurate completion of visit clinical procedures and collection of information for study participants according to clinical protocols, and for protecting the health, safety, and welfare of research participants.
Your participation in any trial is voluntary, and you are free to withdraw from the study at any time, for any reason.
If you or a loved one believes you are at risk for developing one of these conditions – please contact us for more information and we can set up an evaluation to discuss your concerns and possible options. Our study doctor(s) and the team here at Perceptive can meet with you to discuss further details and questions you may have.
About Parkinson’s Disease (PD)
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About Alzheimer’s Disease (HD)
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About Progressive Supranuclear Palsy (PSP)
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About Huntington’s Disease (HD)
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