The importance of standard operating procedures in clinical trials

Journal of Nuclear Medicine Technology

Volumn 41, Issue 3, 2013, Pages 231-233

  Sajdak, Rebecca ^a   Trembath, LisaAnn ^b   Thomas, Kathy S ^c  

^a LOYOLA UNIVERSITY MEDICAL CENTER   (United States)

^b AVID RADIOPHARMACEUTICALS   (United States)

^c Capintec Inc   (United States)

Author keywords

Good clinical practices; Molecular imaging; PET; Protocol; Research methods; Statistics

Indexed keywords

ARTICLE; CLINICAL RESEARCH; CLINICAL TRIAL (TOPIC); DEVICES; GOOD CLINICAL PRACTICE; HUMAN; INFORMATION PROCESSING; MOLECULAR IMAGING; PRACTICE GUIDELINE; QUALITY CONTROL PROCEDURES; STANDARD; STANDARD OPERATING PROCEDURE; WORK ENVIRONMENT;

GOOD CLINICAL PRACTICES; MOLECULAR IMAGING; PET; PROTOCOL; RESEARCH METHODS; STATISTICS;

CLINICAL TRIALS AS TOPIC; HUMANS; PRACTICE GUIDELINES AS TOPIC; REFERENCE STANDARDS;

EID: 84884923556     PISSN: 00914916     EISSN: None     Source Type: Journal    
DOI: 10.2967/jnmt.113.121467     Document Type: Article

References (2)

1. Jackson-Pope L. Tool development to standardize and simplify research practice and support adherence to good clinical practice at clinical trial sites. SoCRA SOURCE. May 2012:11-18.
2. Code of Federal Regulations: title 21-food and drugs. U.S. Food and Drug AdministrationWeb site. http://www.fda.gov/medicaldevices/deviceregulationandguidance/ databases/ucm135680.htm. Accessed June 17, 2013.