I-STAR Network– Advancing Surgical Research, Empowering Pharmaceutical and Medical Device Innovation, Transforming Patient Care.
Partner with Us to Transform Surgical Care
At I-STAR, we are committed to advancing surgical innovation through strategic partnerships with pharmaceutical and medical device companies. Together, we can drive the next generation of treatments, devices, and technologies that will revolutionize surgical care and improve outcomes for patients around the world.
Accelerate Surgical Innovation with the I-STAR Network
The I-STAR network is dedicated to advancing surgical practices through cutting-edge research and collaboration. We understand the vital role that pharmaceutical and medical device companies play in enhancing patient care, and we are here to offer you the support, infrastructure, and expertise you need to transform your innovative products into clinical successes.
Whether you’re developing new pharmaceutical therapies or pioneering medical devices, I-STAR is your partner in driving surgical innovation and improving patient outcomes. With our comprehensive reach in the Irish clinical research space, we can help you accelerate the development, testing, and application of your products in the surgical space
Why Work with the I-STAR Network?
- End-to-End Research & Clinical Trial Support:
I-STAR offers a full range of services to support pharmaceutical and medical device companies at every stage of the product lifecycle. From preclinical studies and early-phase trials to post-market evaluations, we provide tailored solutions for study design, patient recruitment, regulatory compliance, data management, and clinical implementation. - Patient-Centred Research:
I-STAR-supported trials are grounded in a patient-first approach, ensuring that all studies are designed to maximize both patient safety and clinical efficacy. Whether you are testing new drugs, devices, or surgical techniques, our patient-centric model helps ensure better outcomes and a smoother path to approval. - Expertise in Regulatory Affairs:
Navigating the regulatory landscape is crucial for the success of your product. Our team of experts are well-versed in the regulatory requirements for pharmaceutical products and medical devices. We provide guidance on meeting national and international standards, facilitating the approval process and minimizing delays. - Collaboration with Multidisciplinary Experts:
NSRSC fosters a collaborative research environment that brings together experts from surgery, clinical research, data science, and regulatory affairs. This multi-disciplinary approach allows for innovative solutions that address complex challenges in surgical care and product development
Services for Pharmaceutical & Medical Device Companies
- Clinical Trial Design & Execution:
We assist in the design, development, and execution of clinical trials, ensuring scientifically sound, ethically compliant, and effective studies. Our expert team helps you navigate the complexities of clinical trials, from initial planning through to final analysis. - Patient Recruitment & Retention:
NSRSC provides access to a broad and diverse patient population, helping you meet recruitment targets on time while maintaining high retention rates. We leverage our deep understanding of patient care to optimize recruitment strategies and ensure successful trial completion. - Data Management & Statistical Analysis:
We offer advanced data management solutions and statistical analysis services, ensuring the integrity and reliability of your clinical data. Our robust systems help you manage large datasets, analyze results, and generate actionable insights that can drive your product development forward. - Regulatory Compliance & Support:
NSRSC helps you navigate the regulatory complexities of product development, ensuring compliance with national and international guidelines. Our team is experienced in facilitating the approval of both pharmaceuticals and medical devices, providing regulatory support at every stage. - Post-Market Surveillance & Real-World Evidence:
Once your product is on the market, the NSRSC offers ongoing support in post-market surveillance and gathering real-world evidence. We help you track product performance, identify areas for improvement, and ensure that your device or drug continues to meet regulatory requirements.