Our Services - Integrated Services
At Tigermed US, our team is
well-equipped to provide a wide range of services.
At Tigermed US, our team is
well-equipped to provide a wide range of services.
Empower your decisions with Tigermed US Integrated Services – unlock hidden insights,
drive innovation, and transform possibilities into actionable strategies for success.
We offer a wide range of Pharmacovigilance (PV) services to support the safety monitoring and regulatory compliance of your products and to ensure the protection of trial participants and the integrity of the trial data. Our tailored Safety Monitoring and Pharmacovigilance Plans facilitate effective and high-quality safety data collection and assessment of SAE/SUSAR/AESI/DLT and potential safety signals, providing your team and data monitoring committee with timely insights of the evolving safety profile and risk/benefit decisions. We prepare evidence-based, integrated data summaries and risk analyses in aggregate safety reports (DSUR, PSUR, and PBRER) to support strategic and effective risk communication with health authorities. We also conduct thorough audits of pharmacovigilance systems to ensure compliance with GVP and relevant global or local regulatory requirements.
Partner with our U.S.-based medical expert team for global medical monitoring services tailored for all phases of clinical research across various therapeutic areas. Available 24/7, our medical monitors provide oversight to address sites’ inquiries, manage safety risks, support subject eligibility review for improved enrollmenTigermed USing advanced data monitoring tools and analytic expertise, we offer proactive monitoring and assessments of emerging efficacy and safety data, ensuring high quality and timely support for your team and data monitoring committees in evidence-based decision-making. We prioritize strict compliance with GCP, protocols, and regulatory requirements to safeguard your trial subjects and research data and integrity across all sites to meet your timelines and operational goals.
We provide tailored and high-quality medical writing expertise across a broad range of therapeutic areas and document types, from IND application to clinical trial to post-marketing writing. With rich experience partnering with pharmaceutical, biotech, and medical device clients, we offer protocol design and medical writing services in oncology, hematology, orthopedics, cardiovascular disease, respiratory, infectious disease, vaccine, etc., and dive into delivering high-quality solutions to meet full regulatory compliance.
We understand a successful clinical trial relies on entering, storing and accessing important data. Tigermed US aims to help biopharmaceutical industry improving R&D effectiveness and efficiency by providing world class data & information solutions. By collaborating with renowned system vendors and enabling thousands of clinical trial projects, we are committed to providing accurate, transparent and convenient access to your data throughout the full lifecycle of clinical development.