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Appendix 2 to the EDI Rules Form Power of Attorney No. ___The City of ___ ___(Date of issue) ___, (Participant\'s full name) represented by ___, (job title, full name) acting under ___, hereby authorizesLast
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Any organization or individual involved in the production, distribution, or sale of drugs or medical devices in the United States may need to comply with 21 CFR 130505.

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21 CFR 1305.05 refers to the Code of Federal Regulations concerning the registration and applications of certain controlled substances under the jurisdiction of the Drug Enforcement Administration (DEA).
Entities that handle controlled substances, such as manufacturers, distributors, and importers, are required to file 21 CFR 1305.05 forms with the DEA.
To fill out 21 CFR 1305.05, an entity must provide accurate information regarding the controlled substances they plan to handle, including the type, quantity, and purpose of handling.
The purpose of 21 CFR 1305.05 is to ensure proper control and regulation of controlled substances, to prevent misuse, and to promote public safety.
Information required on 21 CFR 1305.05 includes the organization's name, address, type of business, and details about the controlled substances involved.
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