Add company in the Clinical Trial Agreement Template

Aug 6th, 2022
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Got questions?

Here are some common questions from our customers that may provide you with the answer you're looking for. If you can't find an answer to your question, please don't hesitate to reach out to us.
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How to Join a Clinical Trial Look for options. Review eligibility criteria. Contact the study organizers. Review the study description. Learn about informed consent.
Many different types of people take part in clinical trials. Some studies include healthy volunteers, while other studies include patient volunteers. Some studies include both healthy and patient volunteers .
Clinical Trial Agreements (CTAs) require signatures from both the trial sponsor and a University institutional official (IO) with signature authority delegated by the Board of Trustees of the Leland Stanford Junior University.
Key Distinctions Between CTAs and INDs One primary distinction to note between a CTA and an IND submission is that the CTA is protocol-specific, while the IND is product-specific. Once the CTA is submitted, the EU requires a new CTA for any new protocols amended.
Pharmaceutical, biotechnology and medical device companies initiate, manage and fund clinical trials and are ultimately responsible for the clinical trial process. They are referred to as sponsors.
Parties to clinical trial or study agreements include the participating site, the study sponsor, and/or the relevant clinical research organization (CRO).
Sponsor: The person or group of people who supervise or fund the trialsuch as a drug company. Participant: A person who volunteers to take part in the clinical trialsuch as yourself! Investigator: A researcher who helps conduct the clinical trialsuch as a doctor.
A CTA serves as a legally binding contract between a sponsor, site, and researcher, and outlines each partys responsibilities and obligations for the clinical trial.

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