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Employee Spotlight: Kevork Khorozian’s Journey of Courage and Resilience Earns Recognition Within Client Organization

At ClinChoice, we’re proud to celebrate the remarkable contributions of our team members—professionals who bring to the table not only…

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Employee Spotlight: Kevork Khorozian’s Journey of Courage and Resilience Earns Recognition Within Client Organization

At ClinChoice, we’re proud to celebrate the remarkable contributions of our team members—professionals who bring to the table…

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Breaking Down FDA’s Accelerated Approval Updates – A Focus on Confirmatory Trials

The FDA’s Accelerated Approval (AA) pathway, introduced in 1992 amid the HIV/AIDS crisis, has played a pivotal role…

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Toward a Greener Future: ClinChoice Armenia’s Tree-Planting Initiative

At ClinChoice, Corporate Social Responsibility is more than a principle, it’s a commitment woven into the DNA of…

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Understanding the Standard for Exchange of Nonclinical Data (SEND)

Adapting your study data to evolving standards presents numerous considerations in order to ensure your study data is…

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Considerations for Applicants Following the Introduction of the Center of Drug and Medical Technology Expertise

Significant changes have been made in the regulatory landscape governing medicinal products in Armenia. Effective April 25, 2024,…

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Custom-Made Medical Devices: Are You Complying With EU Requirements?

The world is progressing rapidly with advanced technologies and customization in almost every sector to meet human needs.…

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Project FrontRunner: Advantages in directing oncology therapy development to an earlier clinical setting

What is Project FrontRunner? Project FrontRunner is an Oncology Center of Excellence (OCE) initiative that encourages sponsors to…

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Informed Consent: Guidance for IRBs, Clinical Investigators and Sponsors

In August of 2023, the Food and Drug Administration (FDA) released a final guidance document that serves to…

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New EU MDR compliance dates: Impact assessment and next steps

MDR transition Regulation (EU) 2017/745 on medical devices (MDR) has replaced the dated Medical Device Directive 93/42/EEC (MDD)…

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