Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.

Skip to main content

Table 1 Further information requested to support initial applications

From: Capacity for ethical and regulatory review of herbal trials in developing countries: a case study of Moringa oleifera research in HIV-infected patients

Domain

IERC 1

IERC 2

NDRA

NEC

NRC

Details of research procedures

X

X

X

X

 

Details of informed/storage consent

X

X

 

X

 

Reimbursement

 

x

x

  

Details of research design

 

X

X

  

Pre-clinical data to justify human studies

  

X

  

Details of adverse event monitoring

 

X

   

Details of product standardization and quality

 

X

X

  

Adequacy of clinical trial site infrastructure

  

X

  

Re-consenting of participants for specimen shipment

    

X