Independent IRB offers drafting of informed consent forms as a service to its clients.
To request this service submit a Research Protocol, Investigator’s Brochure/Product
Information, payment information, and any other relevant information. The IIRB,
Inc. will forward a draft ICF in approximately 48-72 hours. For more information
contact Independent IRB office.
The responsibility for initial determination as to whether an activity constitutes
human subjects research rests with the investigator. Independent IRB provides confirmation
of human subject research determination as a service to its clients. To request
a confirmation for human research determination, submit a copy of the Research Protocol.
Independent IRB's determination will be forwarded to the Investigator.
Independent IRB provides exemption determination as a service to clients. To request
this service submit a Request for
Exemption Determination Form. Independent IRB's determination will be forwarded
to the Investigator. For more information
contact Independent IRB office.
Independent IRB can serve as a HIPAA Privacy Board and can provide consultation
for Information Plan development.
Independent IRB offers onsite training individualized to the needs of the Sponsor
or Site. For more information
contact
Independent IRB office.
Independent IRB requires that the Principal Investigator has education and training
in Human Research Protection (HRP). There are numerous programs available to interested
researchers and Independent IRB will accept documentation from these training programs
as evidence of compliance with this requirement. If an Investigator does not have
documentation of HRP training, Independent IRB provides access to a program for
this purpose. This training program is known as Collaborative Institutional Training
Initiative (CITI). For more information, see
HRP Training.
Independent IRB is dedicated to ensuring that research participants are provided
with adequate information about clinical research trials. In efforts to do this,
each of our Informed Consent Form contains information to take them to an Independent
IRB website that will provide them with additional information.
On this website research participants will be provided information about their rights
as a research participant, key terms in clinical research, additional resources
on clinical research, and a place to send their comments to Independent IRB.
Click
here if you like to view
this website for research participants.