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483
•Rho, Inc.•June 30, 2017

Rho, Inc. – FDA 483, Jun 30, 2017

Record Details

Rho, Inc., a Contract Research Organization in Chapel Hill, NC, received a Form 483 following an inspection from June 26-30, 2017. The inspection revealed a failure to ensure investigations were conducted according to the investigational plan and IND protocols. This led to issues with subject randomization and the supply management of investigational products at clinical sites.

Company
Rho, Inc.
Inspection date
June 30, 2017
Product type
drugs
Office
New Jersey District Office
People
  • Jean Mulinde (other)
  • Michael Serrano (investigator)
View Company Profile

ID · 78a0906f-65e8-49bf-8a18-7a1e14020908

Other documents for Rho, Inc.
  • EIR - 2017-06-30June 30, 2017

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