Skip Navigation

Regulatory Compliance and Human Subjects Protection Branch (RCHSPB)

Skip Content Marketing
  • Share this:
  • submit to facebook
  • Tweet it
  • submit to reddit
  • submit to StumbleUpon
  • submit to Google +

Mission Statement

RCHSPB's mission is to facilitate the clinical research enterprise by providing protocol development and regulatory, clinical trials management and safety oversight for the NIAID intramural and Division of Clinical Research (DCR) programs.

RCHSPB originated in June 2001. Branch staff consists of a Branch Chief, Clinical Research Oversight Managers, and administrative support personnel. A contract with SAIC-Frederick, Inc., provides staffing for key areas of the support that the branch provides. Each oversight manager is responsible for an area of research support and oversees the contract staff’s work.

Open All

Clinical Safety Office

 

Clinical Trials Management (CTM) Group

 

NIAID IRB Office

 

NIAID Regulatory Review for Intramural Protocol and Informed Consent or Assent Documents

 

Regulatory Group

 

Training

 

Contacts

RCHSPB Staff

Last Updated September 02, 2011