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Scientific writers and clinical evaluation reports (CERs)
Scientific writers can help you with your clinical evaluation needs. Clinical evaluation is an ongoing requirement for...
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An Introduction to Implementing CDISC Study Data Standards
Importance of Study Data Standards Exchanging data globally has become much simpler as information technologies develop. However,...
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ISO 10993-17 Revision
The new version of ISO 10993-17 is expected to be published very soon. This is a major...
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Effective management of your clinical trial budget
Successfully executing a clinical trial is a large undertaking that requires strategic planning and cooperation. Even if...
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AIMD MRI safety
We recently updated our website to highlight our capability of evaluating the MRI safety of active implantable...
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Mid-Sized CRO Benefits
If you have decided to seek a CRO for a forthcoming study need, there are many benefits...
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Is your CRO providing the customer service and flexibility you need?
Over the last several years, there have been rapid changes in the industry. Most notably, there has...
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RF-Induced Heating of AIMDs
Next month, we will be presenting at the National Institutes of Health (NIH) as part of the...
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What is a contract research organization (CRO)?
A Contract Research Organization (CRO) is a company that provides clinical trial services for the pharmaceutical, biotechnology,...
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What is regenerative medicine?
Regenerative medicine is an interdisciplinary field that integrates engineering and life science principles to develop and deliver...
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Clinical evaluation reports (CERs) and working with scientific writers
Clinical evaluation is ongoing and necessary for medical device manufacturers. A manufacturer that sells its products in...
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Creating a Robust Clinical Evaluation Plan (CEP)
A clinical evaluation plan (CEP) may be necessary for your device. A medical device manufacturer that sells...
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