Frequently Asked Questions

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ECNE Research provides specialized consulting services across the product lifecycle, supporting life sciences companies with tailored solutions in clinical-regulatory strategy, clinical research, evidence generation, and market access. Our team of in-house experts and extensive network of practicing consultants bring up-to-date insights and deep therapeutic area knowledge to help clients navigate complex healthcare landscapes. From regulatory submissions and clinical trial design to real-world evidence generation, pharmacovigilance, and strategic market positioning, ECNE Research delivers precise, actionable results to drive your success at every stage.

Our initial consultation is free of charge. This first meeting allows us to understand your needs, discuss your goals, and determine if there’s a potential fit for partnering together. After the initial consultation, we offer flexible pricing options based on your project’s scope—clients can choose either a comprehensive project rate or an hourly consultancy rate, tailored to best meet their needs.

Our leadership team are based in the United States and Ireland. Our writing and operations team are all US-based. One of the things that sets us apart from other medical writing and clinical research companies is that within our team, we have practicing clinicians (physicians, nurses) with vast experience across many healthcare specialties. 

We work with regulatory teams, medical affairs team, quality and safety teams in the pharmaceutical and medical device industries. Our services are suitable for medical device and pharmaceutical companies requiring support with clinical research (e.g., study design, data analysis, study reporting) and clinical documentation (e.g., for regulatory submission, publication). 

We spend time getting to know you and your specific needs. We believe in regular project updates and seek extensive input from our clients before finalizing an execution plan. We engage our dedicated in-house team and extensive network of practicing consultants to provide tailored support across the entire product lifecycle, from regulatory strategy and clinical trial management to real-world evidence generation and market access, ensuring compliance and optimizing outcomes. Our flexible, client-focused approach allows us to quickly adapt to your needs, making us a reliable partner in navigating complex healthcare and regulatory landscapes to drive successful project results.

We deliver customized solutions and high-quality documents efficiently in the shortest time possible. Timelines will depend on the client's needs and timelines, as well as the scope of the project. 

Our primary focus is ensuring quality and excellence across all our deliverables and services. We establish strong, professional relationships based on trust and responsive communication. 100% of our customers are extremely satisfied with the quality of our services and 100% of our customers have found it extremely easy to do business with the ECNE team. 

We understand the fast-paced start up world and offer tailored clinical and regulatory support services to streamline your research, reduce costs, and help you scale with confidence. First consultation is free of charge.