Solutions Focused Full-Service CRO Specialising In Ophthalmology, Oncology, And Rare Disease

GreenLight Clinical can assist with all aspects of study feasibility, startup and works with our wide network  of sites including on site identification, selection, ethics and regulatory submissions, and contract negotiations. Our team has a deep understanding of local regulations and requirements, ensuring a smooth start to your clinical trial.

Our experienced project managers provide efficient and effective oversight of your clinical trial. With a focus on communication, timelines, and risk management, we ensure that your study stays on track and within budget.

At GreenLight Clinical, we understand the importance of closely monitoring site activities to ensure compliance with relevant guidelines and regulations;the protocol, patient safety and data integrity. Our experienced CRAs conduct on-site visits and remote monitoring, as well as providing ongoing site training and support. We work closely with sites to facilitate smooth study conduct, from patient recruitment to data collection and submission. Our team also offers a service of support in budget and contract negotiations, as well as ongoing communication and training for site staff.

Our data management team ensures the accuracy, completeness, and consistency of your clinical trial data. We utilise industry best practice and processes to efficiently collect, clean, and analyse data.

Our biostatisticians provide comprehensive statistical analysis of your clinical trial data. From study design to final reporting, we ensure accurate and meaningful results for your study.

Our team of medical monitors and safety experts provide ongoing oversight and support to ensure patient safety throughout your clinical trial. We also assist with timely and accurate reporting of adverse events in accordance with local regulations and requirements, and understand the importance of pharmacovigilance in ensuring the safety of study participants. Our team is also able to assist with the development of risk management plans and conducts ongoing safety monitoring and reporting.

Our medical writers are experienced in developing a wide range of clinical documents, including study protocols, investigator brochures, and clinical study reports. We ensure all documents adhere to regulatory requirements and guidelines.

Navigating the complex regulatory landscape of clinical research can be challenging. At GreenLight Clinical, our team of experts can assist with regulatory submissions, interactions with regulatory authorities, and compliance with local regulations.