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How wearable technology is optimizing the clinical research industry
The second, in a blog series about how advances in technology are impacting clinical trials. Read part I,...
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How are technological innovations affecting the clinical research process & likelihood of trial success?
The first in a series of blogs about how advances in technology are impacting clinical trials. Technological...
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6 things sponsors or CROs can do to help sites be more efficient in clinical studies
Successful execution of a clinical trial depends upon excellent working relationships between clinical research sites and sponsors....
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IHIF Annual Gala Dinner
On September 13th, MED had the opportunity to be a sponsor at the 2017 IHIF Annual Gala...
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MED Institute welcomes Ted Heise, PhD
For Immediate Release: Bloomington, Ind. – Med Institute Inc. today announced Ted Heise as the new vice...
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5 Tips for Medical Device Sponsors for Running a Successful Clinical Trial
Everyone is demanding more clinical evidence from medical device companies these days. FDA wants to see more...
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Is the Pre-Submission process worth the time and effort?
The last in a series of blogs about informal, pre-submission contact with FDA. Read the first here,...
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What happens once I submit a Pre-Submission? (Part 3: After the meeting)
The sixth in a series of blogs about informal, pre-submission contact with FDA. See here, here, here,...
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What happens once I submit a Pre-Submission? (The meeting)
The fifth in a series of blogs about informal, pre-submission contact with FDA. See here, here, here,...
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What happens once I submit a Pre-Submission? (Before the meeting)
The fourth in a series of blogs about informal, pre-submission contact with FDA. See here, here, and...
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