Connect with NEA Clinical about your upcoming clinical trial
Request a proposal
Connect with NEA Clinical about our upcoming vacancies
Request a proposal
Connect with NEA Clinical about your upcoming clinical trial
Request a proposal
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Why Megalek
MEDICAL DEVICE DEVELOPEMENT
NEA Clinical specializes in the clinical trial development and data management of medical devices specifically.
The design and implementation of medical device studies may vary significantly from the studies of pharmaceutical products. NEA Clinical is able to offer services that are specifically designed to meet the trial needs and regulatory requirements that are unique to the development of medical devices.
Outsourcing to NEA Clinical will save you vital time in the trial and lead to substantial financial savings in medical device development.
The design and implementation of medical device studies may vary significantly from the studies of pharmaceutical products. NEA Clinical is able to offer services that are specifically designed to meet the trial needs and regulatory requirements that are unique to the development of medical devices.
Outsourcing to NEA Clinical will save you vital time in the trial and lead to substantial financial savings in medical device development.
CLINICAL DEVELOPMENT SOLUTIONS OVERVIEW
MEDICAL DEVICE DEVELOPEMENT
NEA Clinical specializes in the clinical trial development and data management of medical devices specifically.
The design and implementation of medical device studies may vary significantly from the studies of pharmaceutical products. NEA Clinical is able to offer services that are specifically designed to meet the trial needs and regulatory requirements that are unique to the development of medical devices.
Outsourcing to NEA Clinical will save you vital time in the trial and lead to substantial financial savings in medical device development.
The design and implementation of medical device studies may vary significantly from the studies of pharmaceutical products. NEA Clinical is able to offer services that are specifically designed to meet the trial needs and regulatory requirements that are unique to the development of medical devices.
Outsourcing to NEA Clinical will save you vital time in the trial and lead to substantial financial savings in medical device development.
Medical device trials used to be smaller than drug trials, but they are no less complex.
Difficult to blind, randomize and control, they demand vast experience and the flexibility and expertise to understand how to leverage user feedback to optimize your product. NEA Clinical team has established strong clinical teams to deliver study quality. We are partnered with key specialist hospital and research facilities giving our clients direct access to the most active and reputable KOLS,PIs and sites to facilitate study start-up and patient recruitment to deliver on clinical timelines.
Our clinical, regulatory and marketing services focus on bringing medical devices to market and then supporting them throughout the life cycle. We dedicate resources to every project, working as part of your team.
Difficult to blind, randomize and control, they demand vast experience and the flexibility and expertise to understand how to leverage user feedback to optimize your product. NEA Clinical team has established strong clinical teams to deliver study quality. We are partnered with key specialist hospital and research facilities giving our clients direct access to the most active and reputable KOLS,PIs and sites to facilitate study start-up and patient recruitment to deliver on clinical timelines.
Our clinical, regulatory and marketing services focus on bringing medical devices to market and then supporting them throughout the life cycle. We dedicate resources to every project, working as part of your team.
Our full-service support coupled with our vast expertise across therapeutic areas maximizing results.
Our full-service support coupled with our vast expertise across therapeutic areas maximizing results.
NEA Clinical has years of experience in regulatory affairs. We support all kinds of trials for Class I, II, III medical devices, to help you collect high quality, ISO14155, compliant clinical data. Our services include:
- Feasibility
- Site Selection
- Study Start Up
- Project Management
- Clinical Monitoring
- Vendor Management
- Data Management
- Biostatistics
- Medical Monitoring
- Medical Writing
- Quality
- Legal Representation
- Regulatory Services