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Compliance In Focus

remote services

LEARN MORE ABOUT REMOTE SERVICES

Keep Your Clinical Trial Moving from a Distance

You want to keep your trial on track, but physical distancing and travel restrictions have made it difficult. Fortunately, IMARC has experience providing remote services.

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Posted by John Lehmann on Wed, Jan 03, 2018

Building the Business Case for Clinical Research Training

Most clinical research study sponsors recognize that having a properly trained research staff is key to ensuring compliance and bringing their device to market faster. The question is, how do you implement an effective training program that achieves your organization’s desired goals?

Topics: IMARC University, Clinical Research Training, Building a Business Case

Posted by John Lehmann on Wed, Jan 03, 2018

What Makes Good Clinical Research Training?

We have noticed an increase in the demand for training across the clinical research landscape. This should come as no surprise with the constant advances in technology improving the way that clinical research studies are conducted. Those of us involved in this privilege are continually striving to keep up, and continuing education is a regular part our profession. In addition, FDA regulations require that individuals involved in the clinical research process be qualified by training and experience. But what constitutes “adequate” training? This a question often asked of us by the sponsors and investigators we work with.

Topics: IMARC University, Clinical Research Training

Posted by Shawn Kennedy on Wed, Jan 03, 2018

What Makes Good Clinical Research Training?

Recently, we have noticed an increase in the demand for training across the clinical research landscape.  This should come as no surprise with the constant advances in technology improving the way that clinical research studies are conducted.  Those of us involved in this privilege are continually striving to keep up, and continuing education is a regular part our profession.  In addition, FDA regulations require that individuals involved in the clinical research process be qualified by training and experience.  But what constitutes “adequate” training?  This a question often asked of us by the sponsors and investigators we work with.

Topics: FDA Regulations, IMARC Research, Clinical Research Training