The FDA regulations (21 CFR 312.3): Is it allowable that IND sponsor involves more than one individual or organization?

#1
The FDA regulations (21 CFR 312.3) define theSponsorof the IND application asthe person who takes responsibility for and initiates a clinical investigation. The Sponsor may be an individual or pharmaceutical company, governmental agency, academic institution, private organization, or other organization. But it doesn't imply clearly about the number of the IND sponsor, is it allowable that IND sponsor involves more than one individual or organization?
Thanks a lot
 
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