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studies can answer questions about long-term exposures, 
since the average period of device use in these studies was 
around three years.
5. What research is needed to decide whether RF exposure 
from tablets poses a health risk?
A combination of laboratory studies and epidemiological 
studies of people actually using tablets would provide some of 
the data that are needed. Lifetime animal exposure studies 
could be completed in a few years. However, very large 
numbers of animals would be needed to provide reliable proof 
of a cancer promoting effect if one exists. Epidemiological 
studies can provide data that is directly applicable to human 
populations, but ten or more years follow-up may be needed 
to provide answers about some health effects, such as cancer. 
This is because the interval between the time of exposure to a 
cancer-causing agent and the time tumors develop — if they 
do — may be many, many years. The interpretation of 
epidemiological studies is hampered by difficulties in 
measuring actual RF exposure during day-to-day use of 
tablets. Many factors affect this measurement, such as the 
angle at which the tablet is held, or which model of tablet is 
used.
6. What is the FDA doing to find out more about the possible 
health effects of tablet RF?
The FDA is working with the U.S. National Toxicology Program 
and with groups of investigators around the world to ensure 
that high priority animal studies are conducted to address 
important questions about the effects of exposure to Radio 
Frequency (RF) energy. 
The FDA has been a leading participant in the World Health 
Organization International Electro Magnetic Fields (EMF) 
Project since its inception in 1996. An influential result of this 
work has been the development of a detailed agenda of 
research needs that has driven the establishment of new 
research programs around the world. The project has also 
helped develop a series of public information documents on 
EMF issues. 
The FDA and the Cellular Telecommunications & Internet 
Association (CTIA) have a formal Cooperative Research And 
Development Agreement (CRADA) to do research on wireless 
device safety. The FDA provides the scientific oversight, 
obtaining input from experts in government, industry, and 
academic organizations. CTIA-funded research is conducted 










