Maintain Safe & Effective Usage

Eliminate the risk of complexity

A Fit-For-Purpose Solution

  • What are your challenges?

    In today’s global marketplace, pharmaceutical manufacturers need an organized and integrated medical information and pharmacovigilance service model to safely distribute therapies in varying government and regulatory structures.

  • What does success look like?

    You need to monitor the safety risks of a commercial product, compliantly answering patient inquiries and accurately reporting adverse events that contribute to market success. You need to be diligent about integrating post market safety surveillance requirements and the delivery of high-quality medical information that protects you from major financial risks and improves patient outcomes.

  • Why EVERSANA?

    As a single, integrated service partner, EVERSANA delivers programs with the infrastructure, technology, workflows and clinical staffing needed to effectively and efficiently support therapies on a global scale, from Europe to Asia and beyond.

The rapidly evolving needs of our global clients

need to be addressed with new thinking.

 

 

Why partner with EVERSANA
to Maintain Safe & Effective Usage of your drugs?

  • Holistic View

    Isolated, siloed activities executed by a number of vendors are not as impactful on the patients’ adherence; therefore, using a single platform for the commercialization of your products will result in higher levels of effective and safe usage of your products. From PharmDs to Field Solutions reps, we are working for your product’s commercial success.

  • Valued Partner

    No other partner can provide the depth, breadth, scale and intimacy our team can provide across ALL three key stakeholders for your business – the Patient, the Payer and the Provider.

  • Our guarantee!

    Our customized services are based on our leading industry experience and we have the case studies and results to guarantee it.

Regardless of the region or language

our clients must provide therapies to patients safely and efficiently.

View our Case Studies

  • FDA Approves small clinical trial
    FDA Approves small clinical trial

    We supported a client to get FDA approvals for an ultra-rare therapy. Initially the small population was a concern.

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  • New contact team in under 7 days
    New contact team in under 7 days

    A sudden transfer of ownership for an immunotherapy product required access to a call center staffed with PharmDs. Our team had them covered in under 7 days.

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Sample Results Across Our Business

  • 99%
    Inquiries Answered live by PharmDs
  • 95%
    Timely closure of cases Medical device complaints managed closure in less than 60 days
  • 100%
    Regulatory compliance 100% of adverse events processed within specified regulatory timeframe

Value is achieved with Comprehensive Services, including:

  • Market Access Strategy & Stakeholder Engagement

    Breaking down the complexity of reimbursement and access. Engaging the Patient, Payer and Provider.

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  • Medical Information/Pharmacovigilance

    Reduce risk by focusing on safety and effectiveness.

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  • Adherence Support

    Drive awareness, education and support services to promote adherence and better health outcomes.

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  • Patient Services/HUB

    Patient programs to help patients navigate the complex onboarding process.

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  • Field Solutions

    Fully resourced to support a rapidly sophisticated, clinically-oriented and data-driven operation.

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Speak with an expert today