Sec. 30. (a) Sections 16 and 20 of this chapter do not apply to the actions of a: (1) person who is employed or retained as an investigator by a pharmaceutical manufacturer described in subdivision (3); (2) practitioner; or (3) pharmaceutical manufacturer that is approved by the federal Food and Drug Administration; performed in an investigation of a pharmaceutical manufacturer's legend drug that is suspected of being counterfeited, adulterated, or misbranded. (b) A drug sample collected during an investigation described in subsection (a) may only be used for testing or a civil or criminal action. A drug sample collected during an investigation may not be resold or provided for human consumption. (c) A pharmaceutical manufacturer that collects drug samples during an investigation described in subsection (a) shall: (1) maintain records of the drug samples; and (2) make these records available, at a reasonable time, to law enforcement agencies or the agencies' representatives in the enforcement of this chapter. IC 16-42-20 Chapter 20. Drugs: Enforcement of Pharmacy Laws and Rules 16-42-20-1 Powers of enforcement officers 16-42-20-2 "Controlled premises" defined; administrative inspections and warrants 16-42-20-3 Injunctions 16-42-20-4 Cooperative arrangements and confidentiality 16-42-20-5 Forfeitures 16-42-20-6 Burden of proof; liabilities 16-42-20-7 Judicial review 16-42-20-8 Education programs 16-42-20-9 Research 16-42-20-10 Contracts for educational and research activities 16-42-20-11 Anonymity of research subjects 16-42-20-12 Possession and distribution of controlled substances for research purposes
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