easyClinical Supports Innovative MedTech Solutions

We support MedTech companies in both clinical evaluation and clinical investigation through generating robust clinical evidence to get their products authorized on the market and advancing medical innovation.
easyClinical supports innovators with all requirements for all risk classes of their device-Class, including Post market clinical follow-up (PMCF).

 

Clinical Investigation

  • Pre-market study, FIH
  • Post-Market Clinical Follow Up (PMCF)
  • Real-World data collection (retro prospective)
  • PMCF Surveys
Medical device studies

Clinical Evaluation

  • Clinical Evaluation Report (CER)
  • Clinical Evaluation Plan (CEP)
  • Clinical Development Plan (CDP)
  • PMCF Plan
  • Post-Market Surveillance Plan (PMS)
  • Periodic Safety Update Report (PSUR)
  • Summary of Safety and Clinical Performance (SSCP)
  • Claiming Equivalence
  • Labeling
  • Device Risk Management
Clinical Evaulation

Capabilities

Strategy

A business strategy is the means by which it sets out to achieve its desired ends.

Audit

If you have been selected for a business audit, here is what you need to know.

Restructuring

Restructuring your company could restore its viability and improve its liquidity position.

Benefits

Marketing Research

Research helps you plan the best way to get your product from the manufacturer to the retail shelf. In addition to deciding which retailers should carry your product, you should determine where your inventory will be held.

Listen to your team

Go to your team, and tell them you want to make a fresh start. Tell them you want them to enjoy their jobs more and get more done.

Analyze the Problem

In this problem solving step, you will want to figure out what caused the problem, what the problem looks like at this moment, and the urgency of addressing the problem.

Insights

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July 30, 2024
Que fait-il inclure dans un article de blog ? Un contenu utile sur l’industrie, qui : 1)...
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