informed consent process

• Developing cultural competence and overcoming ethical challenges in the informed consent process: an experience from Egypt.

Introduction Research activities are increasing in size, complexity, regulatory oversight, and cost, creating challenges and pressures on the resear...

• Journal of Research Administration
• Vol. 39 Nbr. 2, September 2008

• Krames Patient Education Launches Krames Patient ConsentTM to streamline and enhance the Informed Consent Process.

Innovative tool combines legal form creation and patient education in an easy-to-use electronic application to improve provider-patient communication ...

• Business Wire
• October 07, 2009

• Food and Drug Administration Clinical Trial Requirements, Regulations, Compliance, and Good Clinical Practice

The Food and Drug Administration (FDA) Detroit District Office, in co-sponsorship with the Society of Clinical Research Associates (SoCRA) is announcing a public workshop. The public workshop on FDA's clinical trial requirements is designed to aid the clinical research professional's understanding of the mission, responsibilities, and authority of FDA and to facilitate interaction with FDA representatives. The program will focus on the relationships among FDA and clinical trial staff, investigators, and institutional review boards (IRB). Individual FDA representatives will discuss the informed consent process and informed consent documents; regulations relating to drugs, devices, and biologics; as well as inspections of clinical investigators, IRB, and research sponsors. Date and Time: ...

• Federal Register Nbr. 77 FR 8886, February 15, 2012
• Notices
• Health and Human Services Department

• Regulating Clinical Research: Informed Consent, Privacy, and Irbs

Introduction. II. A Historical Overview of Research Abuses and the Development of Research Regulations. III. The Federal Regulations that Govern IRBs and Informed Consent. A. What Is Regulated?. B. IRBs. C. Informed Consent. D. Research Involving Only Existing Medical Records Or Tissue Samples. IV. Deficiencies in the Regulatory System. A. IRB Workloads. B. Flaws In The Informed Consent Process. C. Informed Consent Is Particularly Difficult To Obtain From Gravely Ill Patients. V. Recommendations. A. IRBs. B. Informed Consent Procedures. C. Storage Of Blood And Tissue Samples For Future Genetic Testing. VI. Conclusion.

• Capital University Law Review
• Nbr. 31-1, January 2003

• Business Headlines

Standard Register to acquire company DAYTON -- The Standard Register Co. has a deal to acquire Atlanta- based Dialog Medical, a company that specializes in managing the patient informed consent process. Dialog Medical, which has approximately $5 million in annual revenue, will be operated as a wholly owned subsidiary of Standard Register.

• Dayton Daily News
• May 31, 2011

• M. D. Anderson Cancer Center Selects Dialog Medical to Automate Informed Consent Process.

ATLANTA -- World-renowned cancer hospital expands capabilities of its state-of-the-art electronic medical record (EMR) via integration with the iMedCo...

• Business Wire
• May 22, 2006

• Using spiritual interventions in practice: developing some guidelines from evidence-based practice.

... is perhaps best viewed as an ongoing process. Initially, practitioners should determine clients... used, it should be fully explained and informed consent obtained (Miller, 2003). As postmodernism ...

• Social Work
• Vol. 56 Nbr. 2, April 2011

• Stricter Abortion Rules Ok'd Building Codes, Informed Consent Steps Both Likely to Make Process More Difficult

The Indiana House passed two sweeping bills Wednesday that could close abortion clinics and add more steps to the process of getting an abortion. House Bill 1080 would institute building code rules that abortion- rights advocates say would shut down all nine abortion clinics operating in Indiana.

• Evansville Courier & Press
• February 03, 2006

• Dialog Medical Completes Nationwide VA Installation; All 162 VA Hospitals Are Currently Using Dialog Medical's iMedConsent(TM) Application to Standardize the Informed Consent Process.

ATLANTA -- Dialog Medical, the leading provider of informed consent and patient education systems for hospitals and physician practices, today announc...

• Business Wire
• September 22, 2005

• The exploration of role induction as a potential method for improving men's perceptions of career counseling.

... men's engagement in the therapeutic process (Kiselica, 2001; Wester, 2008). However, the limit... the website and were directed to an informed consent letter. This process continued until we ha...

• Career Development Quarterly
• Vol. 59 Nbr. 3, March 2011