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News & Events

ACRP-Avoca Quality Congress (Postponed)

May 1, 2020 | Seattle, WA
Adding Electricity to Patient Centricity: Energizing Solutions - Join patients and executive leadership from sponsors, CROs, sites, and technology suppliers in a collaborative, solutions-focused discussion of the patient centricity landscape. Industry leadership will unveil recent trends in the use of patient-centric tools and technologies and lead an […]

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Avoca Quality Consortium Open Mic – Provider Qualification (AQC Members only)

April 9, 2020 | 11:00am – 12:00pm EDT
Join Janis Hall, AQC Leadership Advisory Board Members, and fellow AQC Members for the AQC’s first Open Mic session where we will answer questions about Provider Qualification, such as, “What do you share with regulatory inspectors when asked to show evidence of provider prequalification?” and […]

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Virtual Meeting: Innovative Solutions to Provider Qualification Challenges

April 6, 2020

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COVID-19 CEO Letter

March 25, 2020 – This is an update on how we are addressing the needs of Avoca’s clients and Quality Consortium Members, and the companies that we are working with as part of the Diligent® Qualification Platform, given the extraordinary circumstances that we face with COVID-19. The Avoca Group Operations Avoca and its global team of experts have […]

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News Release: CRO and Sponsor Quality Award Finalists Announced by ACRP, The Avoca Group

March 6, 2020
Washington, DC – The Association of Clinical Research Professionals (ACRP) and The Avoca Group will jointly recognize leading Sponsors and CROs at the ACRP Awards & Recognition Ceremony on Friday, May 1, during the ACRP 2020 annual conference in Seattle, Washington.

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Article: Clinical Development Vendor Qualification: “Check-The-Box” Exercise?

March 4, 2020 – Contract Pharma – Jay A. Turpen, Senior Consultant, The Avoca Group – Key first steps to vendor risk management. Are your company’s clinical development vendor qualification (VQ) activities a “Check-The-Box” exercise because someone said that regulators expect it? Or are your VQ activities a comprehensive first step in managing the risk […]

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ExL’s 4th European Clinical Quality Risk Management Forum

24–25 February 2020 | London
Join Avoca's session, "Define the Framework and Critical Elements of an Effective Oversight Plan: ICH E6 (R2) Requirements for Vendor Oversight."

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Webinar: When Navigating Risk in Clinical Trials, It’s Best to Mind Your CTQs and QTLs

February 18, 2020 | 11:00am – 12:00pm EST
In this webinar, Crissy MacDonald, Executive Director, Client Delivery, The Avoca Group, will discuss the Quality Tolerance Limit requirements of ICH E6 (R2) and the intersect of Section 3 of ICH E8 (R1), where specific focus is given to proactive quality-by-design in clinical trials, including identifying and managing critical-to-quality factors (CTQs).

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