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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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FDA grants MED Institute MDDT (Medical Device Development Tool) qualification
West Lafayette, IN: MED Institute obtained FDA qualification of their MDDT (Medical Device Development Tool) for virtual...
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MRI Safety Labeling of Medical Devices: Change Is on the Horizon
If you missed us at RAPS Convergence 2021, you can reach out to our team and we...
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CRO selection: How to get it right the first time
CRO selection can sometimes be difficult to navigate. “My favorite meeting to have with a CRO is...
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Can the safe history of clinical use be used as justification for biocompatibility of a medical device?
Can the safe history of clinical use (no complaints registered in PMS) be used as justification not...
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FDA grants MED Institute Accreditation Scheme for Conformity Assessment (ASCA)
FOR IMMEDIATE RELEASE: August 18, 2021 Colleen Tennyson MED Institute 855.463.1633 ctennyson@medinstitute.com MED Institute Receives Accreditation through...
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Clinical Trial Start-Up Top 5 Challenges
An efficient clinical trial start-up is essential to the success of a multicenter clinical trial. Initiating a...
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