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   * * IRB Review ServicesFor more than 50 years, we’ve set the standard for IRB
       review through service, expertise, and innovation.
     * IBC Administration & ReviewSince 2000, we’ve provided Institutional
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WELCOME, LABCORP DRUG DEVELOPMENT TEAM

Hi, Labcorp Drug Development, and welcome to the custom microsite built
specifically for you and your team. As a valued client, we are excited to share
a slew of resources with you that I trust will be helpful as we continue our
partnership.


GOOD TO “SEE” YOU HERE!

I’m Troy Brinkman, and I oversee the IRB relationship between WCG IRB and
Labcorp Drug Development. Please consider me your go-to-contact for all of your
IRB needs. I’ve had the pleasure of working with many of you, and it has been a
joy to assist your team as you prepare for upcoming studies, provide insights on
your selected sites, and connect you to the resources available to you and your
team.

To immediately get started on new projects, all we need are a few details about
your study via email (protocol number, number of expected US/Canadian sites in
the study, and anticipated start date). Once we connect on your study, WCG will
provide the following complimentary services:

 * Site list review (how each site works with WCG)
 * Virtual training in the WCG IRB Connexus portal
 * Cost estimate to assist you with PO creation
 * Pre-review of your submission form and addressing your ethical/regulatory
   questions
 * Kick-off call for every new study with your designated Client Partnership
   Director, Sana Ansari

To get started, or to learn more about WCG IRB and the services we can offer,
simply click the EMAIL ME button and I will walk you through some next steps! In
the meantime, please enjoy these resources, and I look forward to connecting
with you!

Troy Brinkman
Director of Business Development
WCG IRB

Contact me:
360.339.3852
tbrinkman@wcgclinical.com

Email TROY

Sana Ansari
Client Partnership Director
WCG IRB

Contact Sana:
984.227.0447
sansari@wcgclinical.com

Email SANA


SUPPORTING YOUR SITES AND INSTITUTIONS

Sites you work with may be new to the WCG IRB ConnexusTM portal, and they may
ask you for help. To ensure your sites are comfortable with the system, we have
published an Orientation Guide that you can download and send directly to them.
Click the button below to download and send to your sites!

DOWNLOAD THE GUIDE






THOUGHT LEADERSHIP & HELPFUL RESOURCES

Read our latest whitepaper on compensating research participants:

READ THE WHITEPAPER

Four key elements to know about the role of IBCs in Gene Therapy trials:

READ THE BLOG POST

Gain insights from our IRB and IBC experts in our “Ask the Experts” Forum:

ASK THE EXPERTS

Learn about changes to clinical research as a response to the COVID-19 pandemic:

VISIT RESOURCE CENTER

Look at WCG IRB’s response to COVID-19 in reviewing over 650 protocols:

SEE THE IMPACT

See how WCG’s site selection reduced enrollment by 6 months for a sponsor:

View case study



STREAMLINE SUBMISSIONS BY 50% WITH THE ALL-NEW WCG IRB CONNEXUS

2:32










The new WCG IRB Connexus supports our commitment to continuously improving the
quality of submissions by raising the bar on transparency and compliance by
deploying state-of-the-art adaptive technology.

Login to WCG IRB Connexus

Quick Guide: Making a Submission







WCG SERVICES: ALIGNED TO YOUR NEEDS THROUGHOUT THE STUDY CONTINUUM



WCG comprises a suite of clinical research services, divided into two operating
organizations: WCG IRB and WCG Clinical Services.

Within our WCG Clinical Services organizations, we support Study Planning & Site
Optimization, Patient Engagement, Scientific & Regulatory Review, and Marketing
Intelligence & Insights.

Email your account representative






CURATED WCG INSIGHTS FOR YOUR TEAM

Whitepapers


VIRTUAL CLINICAL TRIALS: BEST PRACTICES IN MOVING TOWARD A PATIENT-CENTRIC
RESEARCH MODEL

Read More about Virtual Clinical Trials: Best Practices in Moving Toward a
Patient-Centric Research Model
Whitepapers


UNDER THE MICROSCOPE: BIOMARKER AND DIAGNOSTIC TESTS AS FDA-REGULATED DEVICES

Read More about Under the Microscope: Biomarker and Diagnostic Tests as
FDA-Regulated Devices
Whitepapers


CLINICAL TRIAL RECRUITMENT PRACTICES: THE EVOLUTION OF ETHICAL CONSIDERATIONS

Read More about Clinical Trial Recruitment Practices: The Evolution of Ethical
Considerations



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