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
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