Does this protocol involve the use of substances that may pose any health risk (infectious, carcinogenic, toxic, bacteria, viruses, fungi, parasites, cell lines, primary cells, tissue, fluids, blood, recombinant DNA, chemicals, laser or radiation) to humans?
No
List of References
Research Medicinal Plants
Application for Research Studies using Medicinal Plants (Wild or Cultivated)
what is the social value of this research
Research Medicinal Plants
what is the scientific validity
Research Medicinal Plants
what is the environmental advantage in the future
Research Medicinal Plants
what is the economic benefits
Research Medicinal Plants
How to conserve the plant, if it is rare and possesses a valuable biological importance
Research Medicinal Plants
In case of biotechnological plant researches, you should clarify the difference between the biological activity of natural plant fractions or compounds versus the genetically modified plant
Research Medicinal Plants
In the event of important new findings, to whom the Intellectual Property Rights will belong to
Research Medicinal Plants
Acute toxicity
Research Medicinal Plants
LD50
Research Medicinal Plants
Effective dose
Research Medicinal Plants
Side effects
Research Medicinal Plants
The site and date of collection of plants
Research Medicinal Plants
The taxonomical identification of plants by specialized Taxonomist
Research Medicinal Plants
Which part of the plant will be used (i.e., plant organ(s) used in the research)
Research Medicinal Plants
The safety procedures taken to protect or mitigate the side effects of herbal extracts, fractions or compounds
Research Medicinal Plants
The efficacy of herbal samples
Research Medicinal Plants
Consent form
the completed consent form
Purpose of the Waiver Request: Briefly state or summarize the purpose of this waiver
Type of Waiver of Informed Consent Request
List of identifying information you plan to collect or keep a link to
Explain why the research could not practicably be conducted without the waiver or alteration
Please detail your reasons for a waiver to consent below
Explain why the research and privacy risk of the research are no more than minimal
Describe the measures you will take to ensure the waiver or alteration will not adversely affect the rights and welfare of the subjects
Explain how you will, if applicable and appropriate, provide the participants with additional pertinent information after they have participated in the study, or indicate "Not Applicable"
