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Safira Clinical Research Limited
Safira Clinical Research Limited
Improving Patient Experience - one syste...Products
Medical Affairs *
Scientific Communications Development
Strategic Stakeholder Engagement
Defining the Value of Medical Affairs
Evidence Generation
Strategic Communications Planning
Regulatory *
Labeling & Promotions
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Compliance
Transparency & Disclosure
Commercialization *
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Government Policy
Global Market Access
Pharmacovigilance *
Safety Systems
Risk Management
Finance & Investment *
Financial Services
Investment Banking
Quality & Mfg *
Facilities & Equipment
Testing & Release
Quality Management
Production & Supply Chain
Clinical Research *
Real World Data Research
Study Operations & Management
Clinical Reporting
Product Development
Trial Design & Planning
Technology & Operations *
Automation & Efficiency
Data & Analytics
Early Development
Digital Health Solutions
Operations
Informatics Infrastructure
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Medical Affairs *
Scientific Communications Development
Strategic Stakeholder Engagement
Defining the Value of Medical Affairs
Evidence Generation
Strategic Communications Planning
Regulatory *
Labeling & Promotions
Maintenance & Renewals
Compliance
Transparency & Disclosure
Commercialization *
Customer Engagement
Brand Planning & Activation
Market Access & Policy *
Government Policy
Global Market Access
Pharmacovigilance *
Safety Systems
Risk Management
Finance & Investment *
Financial Services
Investment Banking
Quality & Mfg *
Facilities & Equipment
Testing & Release
Quality Management
Production & Supply Chain
Clinical Research *
Real World Data Research
Study Operations & Management
Clinical Reporting
Product Development
Trial Design & Planning
Technology & Operations *
Automation & Efficiency
Data & Analytics
Early Development
Digital Health Solutions
Operations
Informatics Infrastructure
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About
Cloughjordan, Tipperary, IRL
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Safira Clinical Research Limited
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We founded Safira to improve the patient experience during their clinical trial journey. We do this by supporting technology partners and sponsors in designing patient-facing technologies and their use in clinical trial protocols. Safira provides the support services that new companies with innovative technologies are often in need of to bring their technologies into the clinical trial space.
We are the "One Stop Shop" for eCOA services in clinical research for Sponsors, Tech Partners and CROs.
We conduct research with patients to establish a better understanding of how technology in Decentralized Clinical Trials can reduce their burden and at the same time complies with regulatory demands.
We regularly publish our findings in peer-reviewed journals and present at conferences to share our findings. Current topics of interest are BYOD, Wearable Devices, AI/ML and their application in clinical research.
While we have a clear focus on eCOA, we are also experienced in IRT, eConsent and EDC.
We provided User Acceptance Testing as a Service for more than 10 years now and we partner with multiple vendors and sponsors to assure a quality product is released to the end users (patients and site staff)
We offer excellent training to new joiners in the eCOA space and provide advanced training for more experienced peers in the industry.
License Management can be cumbersome and complex. Our dedicated License Management team will take the complexity out of this process and supports Sponsors and CROs to get it right. We also offer license audits to Sponsors to assure compliance with existing contracts and agreements.
We founded Safira to improve the patient experience during their clinical trial journey. We do this by supporting technology partners and sponsors in designing patient-facing technologies and their use in clinical trial protocols. Safira provides the support services that new companies with innovative technologies are often in need of to bring their technologies into the clinical trial space.
We are the "One Stop Shop" for eCOA services in clinical research for Sponsors, Tech Partners and CROs.
We conduct research with patients to establish a better understanding of how technology in Decentralized Clinical Trials can reduce their burden and at the same time complies with regulatory demands.
We regularly publish our findings in peer-reviewed journals and present at conferences to share our findings. Current topics of interest are BYOD, Wearable Devices, AI/ML and their application in clinical research.
While we have a clear focus on eCOA, we are also experienced in IRT, eConsent and EDC.
We provided User Acceptance Testing as a Service for more than 10 years now and we partner with multiple vendors and sponsors to assure a quality product is released to the end users (patients and site staff)
We offer excellent training to new joiners in the eCOA space and provide advanced training for more experienced peers in the industry.
License Management can be cumbersome and complex. Our dedicated License Management team will take the complexity out of this process and supports Sponsors and CROs to get it right. We also offer license audits to Sponsors to assure compliance with existing contracts and agreements.
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