Arete Biosciences: Elevating Clinical Trials with Expertise and Integrity

Written By Brooke McCutchan

You've invested valuable time and resources developing your assay chemistry and designing your instrument and software. Now, as you prepare for clinical validation, the question arises: where will you conduct the clinical trial?

Choosing the right partner for your clinical trials is paramount and at Arete Biosciences, we understand the importance of finding the perfect fit.

Choosing the right partner for your clinical trials is paramount. At Arete Biosciences, we understand the importance of finding the perfect fit. That's why we offer a comprehensive solution through collaboration with Arete’s Clinical Affairs department, notable for their expertise and established network of Principal Investigators (PIs) and clinical sites, with whom they have cultivated relationships over years of clinical research.

Here's why partnering with a reputable CRO like Arete Biosciences can be advantageous:

  • Dedicated Principal Investigators: Our network of clinical sites is comprised of PIs committed to your project, bringing relevant trial experience to the table.

  • Accredited Sites: We ensure that sites are appropriately accredited, adhering to rigorous standards of quality and compliance.

  • Qualified Personnel: Our sites are staffed with qualified personnel who prioritize clinical research, dedicating ample time and expertise to your study.

  • Access to Intended Use Populations: We facilitate access to the requisite target population suited for your product's intended use, ensuring meaningful and actionable results.

  • Secure Facilities: Our sites offer secure spaces for consenting, testing, and storage of specimens, maintaining the integrity and confidentiality of your study.

  • Navigating Contracts: Leveraging our relationships with legal and financial offices, we assist in navigating contract execution at fair and transparent terms.

Clinical trials can span months or even years. Entrust Arete Biosciences to manage your trial with confidence. Our Clinical Affairs team collaborates closely with yours, understanding your product and designing a tailored clinical validation protocol aimed at achieving successful outcomes and bringing your product to market.

With experienced clinical staff available year-round, let Arete Biosciences lead your trial to success.

Brooke McCutchan

Brooke McCutchan brings over 25 years of experience and a diverse background in the medical industry to Arete Biosciences. Brooke began her career as a medical technologist and soon transitioned into training and sales, followed by marketing and program management at Quidel. During Brooke’s tenure at Nanosphere, she served as Director of two departments, Project and Program Management, and Clinical and Regulatory Affairs. Brooke has extensive experience working with companies of all sizes with varying levels of expertise. Brooke has established an impressive network of industry leaders across the country, and through these partnerships, she has brought numerous in vitro diagnostics devices to market (e.g. from feasibility to commercialization). Brooke holds a BS in Medical Technology from the Medical University of South Carolina and a BS in Biological Sciences from the University of South Carolina.

https://www.aretebiosciences.com/about-brooke
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