.png)
Site Management
We offer comprehensive, end-to-end support, from protocol design and monitoring to trial completion and reporting. Our experts provide guidance throughout the entire lifecycle of the trial, ensuring that the trial is conducted per the highest ethical and regulatory standards. Our site management service is streamlined to reduce costs and timelines, allowing for faster delivery of results.
Patient Recruitment
We offer an experienced patient recruitment team that can help you achieve your clinical trial goals. Our services include developing and executing patient recruitment strategies, such as creative marketing campaigns and patient outreach initiatives. We also provide comprehensive patient enrollment tracking and reporting to ensure that your trial stays on track.
Clinical Monitoring
Clinical monitoring is an essential part of clinical trial site management. We manage a pool of experienced clinical research associates (CRAs) that work collaboratively with principal investigators and study coordinators to ensure that clinical trials comply with local and international regulations and standards and that the safety of study participants is maintained.
Regulatory Compliance and Management
We offer comprehensive support to ensure that your clinical trial site is ICH-GCP compliant. We provide support in all aspects of the regulatory process, from pre-trial preparation and submissions to ongoing monitoring and close out. Our regulatory team are always available to answer any questions and provide guidance to ensure your trial runs smoothly.
Clinical Data Management
Clinical data management involves the collection, storage, and analysis of clinical trial data to ensure accuracy and reliability.
Our data management team are the best at what they do. They are experts in developing, managing, and analysing data related to clinical trials, providing valuable insights into the study process. We ensure that all data is compliant with the applicable laws.
Pharmacovigilance
Our Pharmacovigilance service provides comprehensive drug safety monitoring throughout the clinical trial process. We use state-of-the-art solutions to track and analyse adverse events and ensure all safety protocols are met. Our seasoned team of safety experts work closely with study sponsors and investigators to ensure the safety of all participants.
Clinical Trial Supply Chain Management
We provide comprehensive, reliable, and cost-effective clinical trial supply solutions to our clients. Our end-to-end service covers the importation and in-country logistics, storage and distribution of investigational medicinal products, medical devices, lab kits and trial ancillary supplies to clinical trial sites. Our dedicated team has a deep understanding of international and national regulatory landscape which makes us the perfect partner for your trial supply needs.