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… you: Understand the natural history of a disease and its treatment Quantify and characterize product safety Evaluate real-world effectiveness of a health care … Evaluate risk management programs including REMS and EU-RMPs Depending upon your research question, we work with …
… regulatory real-world evidence, epidemiology, and/or drug safety questions. Database research can help you gain insights on: Medication, device, vaccine, and other treatment safety profiles Disease prevalence and public … claims, and registries for several decades. For each project we identify and access the most appropriate …
… and prescribers understand the real-world use, value, and safety of your products. Observational studies are also … Through these methods and by assembling the right project team drawn from our expert pool of survey experts, … Burden/cost of Illness Disease prevalence and incidence Treatment patterns, impact, and adherence Product safety and …
… and expert consulting advice and deep methodological and project experience in all major therapeutic areas . Our … studies, and drug, vaccine, and medical technology safety and effectiveness enables us to align the right … as those to address issues of nonrandom assignment of drug treatment Providing training on epidemiology methods, …
… the potential for additional labelling claims - Inform safety studies and reduce risks of adverse events Abandoned Drugs - Rescue, repurpose, or resurrect compounds that may …
… Real-World Evidence Research Let us help you ensure the safety of your patients by examining and understanding … To understand disease distribution, risk factors, treatment patterns and impact, comorbidities, … of risk minimization interventions, or to evaluate safety and effectiveness of medical products, our …
… Drug Safety in Pregnancy Satisfy Regulatory Requirements With Help … From Our Perinatal Pharmacoepidemiology Research Team The safety of medical products when used in pregnancy is often not well characterized at the time …
… to your research questions—whether the results will be used to inform your drug development and post-approval strategies or place a potential safety signal into the appropriate context. Literature … clinical development programs. Incidence of adverse events among a patient population or those taking a certain …
… Advancements in EU Health Technology Regulation and Lowering US Medicare … the Medicare system is becoming a reality. The first 10 drugs have been selected for the new Medicare Drug Price … sweeping revision of its pharmaceutical legislation — the largest change in 20 years. The new law, expected by 2025 or …
… in 2023. Its impacts are already being felt – the first 10 drugs have been selected for the new Medicare Drug Price … pricing across Europe. In addition, the European Union (EU) has proposed a sweeping revision of its pharmaceutical legislation – the largest change in 20 years. The new law, expected by 2025 or …