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Prototype devices

It is recognized that a manufacturer may wish to submit a small number  of "prototype models" of a device to clinical investigation in order to assess safety and/or performance; and those such prototypes may need to undergo a number of changes prior to large-scale production.
Clinical Research Professional Certifications

Sponsor

Acronym

Name

ACRPCCRACertified Clinical Research Associate
ACRPCCRCCertified Clinical Research Coordinator
SoCRACCRPCertified Clinical Research Professional
NAIMCIMCertified IRB Manager
CCIPCIPCertified IRB Professional
CfPIECMWP
Certified Medical Writing Professional
ACRPCKACore Knowledge Assessment
APPICPICertified Physician Investigator
RACCCRACertified Research Administrator
DIACRCPClinical Research Certificate Program
CfPIE
CCCP
Certified Clinical Compliance Professional
ACRPCTIClinical Trial Investigator (Non-Physician)
CfPIEDMCP
Document Management Certified Professional
CfPIEGRACP
Global Regulatory Affairs Compliance Professional
CfPIEQSRCP
Quality System Regulation Certified Compliance Professional
DIAPMCPProject Management Certificate Program
PMIPMPProject Management Professional
RAPSRACRegulatory Affairs Certification
SQA
RQAP-GCP
Registered Quality Assurance Professional-GCP
ASQ
CBA
Certified Biomedical Auditor
SCDM
CCDM
Certified Clinical Data Manager
SAS
 SAS Certified Base Programmer
SAS
 SAS Certified Advanced Programmer
ISMPP
CMPP
Certified Medical Publication Professional
  		 


Opinion Poll

Which one of the following do you think is the most common reason for participating in clinical trials?
 
This opinion poll provides an informal way for the clinical research community to express its views on current topics. The results are not a scientific poll and do not necessarily reflect the percentages of all clinical researchers who agree with these positions.
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