Agenzia regionale di sanità della Toscana (ARS Toscana)

01/02/2024
23/03/2026
Institution
EU Institution/Body/Agency
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Institution identification

Institution ID

3331203

Institution full name and acronym

Agenzia regionale di sanità della Toscana (ARS Toscana)

Institution countries

Italy

Type of institution

EU Institution/Body/Agency

Institution role

Other

Institution website

ENCePP partner

Yes
Institution description
Tha Agenzia regionale di sanità della Toscana (ARS) is a public research instute that provides technical and scientifical support to the regional government of Tuscany. In paticular, it supports the regional government in the activities related to pharmacovigilance.
Institution details
Experience with collecting data directly from individual patients or respondents:
Yes
Interest in carrying out research that is funded by pharmaceutical companies:
Yes

Contact details

Studies conducted by the institution

Study protocol objective 2_feasibility assessement: Comparative effectiveness and safety studies using the target trial emulation and estimand frameworks (TARGET-EU-FA)
A post-authorisation/post-marketing observational study to evaluate the association between exposure to AZD1222 and safety concerns using existing secondary health data sources (COVID-19)
A Retrospective Cohort Study to Assess Drug Utilisation and Long-Term Safety of Galcanezumab in European Patients in the Course of Routine Clinical Care (I5Q-MC-B002)
ADEPT: feasibility of estimating the risk of adverse pregnancy, neonatal and child outcomes following either in utero ASM exposure through the mother, or peri-conceptional ASM exposure through the father
ADEPT: The utilisation of antiseizure medications in pregnant women, other women of childbearing potential, and men: a multi-database study from 7 European countries
ASPIrin use and colorectal CANcer risk (ASPICAN)
Comparative effectiveness and safety studies using the target trial emulation and estimand frameworks (TARGET-EU)
Comparative effectiveness of insulin vs analogues to prevent complications of diabetes (CER insulin vs analogues)
CONSIGN study: COVID-19 infection and medicines in pregnancy - a multinational registry based study
Data source heterogeneity in multi-database pharmacoepidemiologic studies: a scoping review (DIVERSE)
Estimating prevalence and incidence of acute myocardial infarction in a set of heterogeneous sources of observational health data collaborating in the EMIF Platform
Estimation of background incidence rates of coagulation disorders and the association with COVID-19 vaccines in pregnant population: a multi-database study from 3 European countries
Identification of type 2 diabetes cases in a set of databases participating to the EMIF project
Impact of EU label changes and revised pregnancy prevention programme for medicinal products containing valproate: utilisation and prescribing trends
Non-interventional post-authorization multi-database safety study to assess the risk of myotoxicity, hepatotoxicity and acute pancreatitis in statin-exposed heart failure patients with or without concomitant use of sacubitril/valsartan (Entresto®)
Non-interventional post-authorization multi-database safety study to characterize the risk of angioedema and other specific safety events of interest in association with use of Entresto® (sacubitril/valsartan) in adult patients with heart failure
Pattern of use of incretin-based drugs in clinical practice
Pattern of use of intravitreal drugs with antiangiogenic properties for age-related macular degeneration and other vascular retinopathies (Anti-VEGF drugs)
Patterns of anti-CGRP mAbs use and triptan consumption before and after anti-CGRP treatment initiation: a descriptive drug utilization study in Tuscany region, Italy
Safety clinical outcomes associated with the use of Idarucizumab for severe bleeding/emergency surgery: an observational population based study (Idarucizumab use)
Safety of Paxlovid Among Patients with Moderate or Severe Hepatic or Renal Impairment
Safety of Paxlovid During Pregnancy
SAFETY-VAC: Background incidence estimation of flares of pre-existing chronic diseases using pan-European electronic healthcare data sources.
SAFETY-VAC: Network of Data Sources for Vaccine Safety Evaluation
SAFETY-VAC: Phenotype proposal and rates of immunocompromised populations in real-world data sources.
Strengthening Use of Real-World Data in Medicines Development: Metadata for Data Discoverability and Study Replicability (MINERVA)
Thromboembolic events reported in association with idarucizumab and andexanet alfa: disproportionality analysis of the Food and Drugs Administration Adverse Eventr Resporting System (FAERS) database (Idarucizumab/andexanet alfa & thromboembolism)
Time to treatment intensification in patients receiving metformin+incretin-based medicines versus metformin+other hypoglicemics (Time to treatment intensification with incretins)
VAC4EU Postauthorisation Effectiveness Study of BIMERVAX® Vaccine in Europe
VAC4EU Postauthorisation Safety Study of BIMERVAX® Vaccine in Europe