SGquality

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#1
My question refers to a Research facility planning to undertake preclinical and clinical studies for Schedule III, IV and V drugs.

This facility is in Rhode Island and I wanted to know if the facility registration is required per Drug Enforcement Administration (DEA) directives ? I am trying to contact the department in Rhode Island but unable to get it through.

Could anyone share their experience please ?

Thanks and have a great weekend
 

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