How long do you have to keep data for?

How long do you have to keep data for?

How long do you have to keep data for?

You can keep personal data indefinitely if you are holding it only for: archiving purposes in the public interest; scientific or historical research purposes; or. statistical purposes.

Can a nurse practitioner be a principal investigator?

Nurse practitioners (NPs) are ideally suited to assume roles of principal investigators (PIs) in clinical trials. NPs are trained and authorized to perform physical examinations, make clinical assessments, diagnose and treat diseases, and prescribe drugs, either independently or in collaboration with a physician.

How do you become a clinical investigator?

Steps To Become a Clinical Trial Investigator

  1. Learn about regulations.
  2. Establish the needed infrastructure.
  3. Search for clinical trials.
  4. Complete needed forms.
  5. Prepare for a pre-study visit.
  6. Receive IRB approval.
  7. Sign the contract and budget.
  8. Get ready for a site initiation visit.

What is an investigator-initiated study?

What are investigator-initiated studies? IISs are clinical studies initiated and managed by a nonpharmaceutical company researcher/s who could be an individual investigator, an institution or a group of institutions, and a collaborative study group or a cooperative group.

What is a PI in clinical trials?

The person(s) in charge of a clinical trial or a scientific research grant. The PI prepares and carries out the clinical trial protocol (plan for the study) or research paid for by the grant. The PI also analyzes the data and reports the results of the trial or grant research.

What is a co-pi?

Co-Principal Investigator (Co-PI) A Co-PI is a senior member of the key personnel team whose role is similar to that of the PI in determining the intellectual content, direction, and conduct of the research or program activities.

Who is a sponsor in a clinical trial?

In the conduct of a clinical trial, a sponsor is an individual, institution, company or organization (for example, a contract research organization) that takes the responsibility to initiate, manage or finance the clinical trial,1 but does not actually conduct the investigation.