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Best Practices

Do You Have Visibility into Your CRO’s processes?

Do You Have Visibility into Your CRO’s processes?

July 6, 2021August 25, 2021

We are cost-conscious, financially responsible, and considerate of budgets, yet understand and clearly communicate how additional activities could add value and reduce time to market.

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Does Your CRO Value Every Single Patient?

Does Your CRO Value Every Single Patient?

May 20, 2021August 26, 2021

Every patient counts. While large-scale intricately-designed studies can afford to lose patients, clinical trials for rare patient populations are not buffered for atrophy. ARG emphasizes that every patient is vital; in fact, we place the utmost importance on every data point in every study.

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Is Your CRO Experienced in Clinical Trials With No Clear Pathways?

Is Your CRO Experienced in Clinical Trials With No Clear Pathways?

April 5, 2021September 10, 2021

ARG has “been there and done that” when it comes to operationalizing rare disease clinical trials. Our maturity can be seen in creating deep relationships, which allow us to get things done with no preexisting roadmap.

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Does Your CRO Understand the Ultimate Trial Goal?

Does Your CRO Understand the Ultimate Trial Goal?

May 23, 2019August 25, 2021

ARG’s primary goal is to improve and prolong the lives of the people affected by rare diseases through the clinical trials we manage. We realize our patient-centric approach by carefully cultivating relationships, fostering meaningful communication, and anticipating and addressing all of the challenges in our studies.

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Does Your CRO Innovate To Keep Trials On Track?

Does Your CRO Innovate To Keep Trials On Track?

May 9, 2018June 8, 2021

ARG knows from experience that the willingness to be flexible has fueled our success in rare disease clinical trials, resulting in approvals with over $3B in sales.

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New Resources


ARG Conference and Travel News
Xtalks Webinar: Conducting Early Phase Clinical Trials in the US for APAC Sponsors
The ARG Oncology Academy: “Committed to Furthering Research”
Q & A with Dr. Ignazio Di Giovanna: Implementing EU 536/2014
ARG One of 16 Companies Selected to Participate in Virginia Trade Program

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  • Services
    • Decentralized Clinical Trials
    • Clinical Operations
    • Medical Monitoring
    • Data Management
    • Biostatistics
    • Quality Assurance
    • Drug Safety
    • EU Legal Representation
  • Expertise
    • Oncology
    • Immunology
    • Rare Disease
    • Neurology
  • Technology
    • IT Best Practices
    • IT Case Study
    • IT Partners
  • Careers
    • Benefits
  • About
    • Mission
    • Leadership
    • Scientific Advisory Board
    • Locations
  • Resources
    • Best Practices
    • News
    • Case Studies
    • Papers
  • Blog
  • Contact
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