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Our ability to speed site activation measurably—as well as reduce costs and improve the quality of study results—stems from WCG’s unmatched experience, proprietary Knowledge BaseTM and highly-evolved technologies.

When you engage any WCG Site Activation services, you take advantage of our unmatched connections to all major sponsors and CROs, our data on more than 36,000 (of about 40,000) FDA regulated PIs in the U.S., thousands of clinical trial contracts and budgets worldwide, as well as study performance on 2,700 research institutions in North America.

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Celebrating 50 years as the industry leader in IRB and IBC

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CenterWatch / Clinical Trials Tracking

WCG’s CenterWatch provides executives the leading source of clinical trial progress and results globally to ensure superior performance of your own studies—ensuring that they proceed faster, smoother, and at a lower cost.  Our newsletters, Research Center Profiles, market analytics services, drug approvals database, webinars and white papers make WCG’s CenterWatch your first call for tracking clinical trials.

Visit Centerwatch.com

FDAnews / Regulatory Compliance Intelligence

WCG’s FDAnews gives regulatory and quality executives the most thorough, up-to-date understanding of inner workings at the FDA and EMA and how they’re likely to alter your development and manufacturing strategies.  If you’re looking to ensure successful regulatory inspections and audits, you’ll value our 483s database, eLearning, webinars and conferences on manufacturing quality assurance, compliance and risk mitigation.

Visit FDANews.com

KMR Group / Study Performance Data

WCG’s KMR Group helps pharmaceutical executives compare their product development processes, performance and cycles using data from 650,000 clinical study sites globally. Use KMR Group statistics to speed enrollment, select highest-performing sites, navigate CRO outsourcing, plus reduce trial expenses and study cycle times. Our Forums allow pharmaceutical executives to exchange R&D performance strategies, our clinical programs help clinical groups benchmark their performance, while our R&D General Metrics Study establishes standards for the biopharmaceutical industry.

Visit KMRGroup.com

MCC / Clinical Trials Standards

WCG’s MCC (Metrics Champion Consortium) compiles metrics, derives benchmarks and assesses performance of clinical trials to help pharmaceutical and medical device member companies set goals and standards for their product development.  By helping you understand how our industry is changing and how others are responding, you’re able create processes and strategies that move you more quickly and inexpensively to study launch, completion and product marketing.  Our reports cover clinical site payments, site data entry, clinical development key performance indicators and risk management practices.

Visit Metrictchampion.org

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Protocol Development

Our experts develop inclusion and exclusion criteria and provide other protocol design services that involve genetic components, such as planning and executing advisory board meetings with physicians to collect their feedback and increase their participation. We also assist Sponsors and CROs with identifying sites and analyzing the geographic distribution of referring providers to increase the probability of trial success.

Patient Identification

We identify potentially eligible patients through outreach programs and InformedDNA’s internal patient database. Through our partnership with InformedDNA, we also offer individualized genetic counseling and screening appointments. Genetic counselors collect detailed medical and family histories during screening programs, which helps Sponsors and CROs determine inclusion/exclusion criteria for their trials.

Patient Engagement

We aid patient support groups, foundations and organizations with patient support services by adding genetics experts to their care teams and by helping direct patients into genetic counseling and screening appointments. Our well-informed experts provide medical management guidance to patients and physicians, improving patient care and increasing provider satisfaction.

Data Collection & Utilization

We collect the appropriate patient experience data and use it to build the patient input and clinical development plan documents that regulators require. We also work with Sponsors and CROs to collaboratively publish or present data they obtained either through a clinical genetic counseling program or through a review of literature and natural history studies that contain genotype/phenotype data.

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Site Identification

Match your study’s therapeutic approach and protocols precisely to site and investigator performance track records, reducing site identification from the 8-10-week industry average to as quickly as seven days.

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Site Contracting

Our expert legal focus, plus our vast Knowledge Base™ of global contract terms and costs cuts your clinical trial negotiating cycles by up to 45%—plus reduce study costs.

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Pretty cool, eh?

Learning Management

Launch fully-automated, 24/7 online site training solutions that significantly cut complexity, time and expense while ensuring full compliance.

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Site Feasibility

Engage and assess the world’s most highly qualified clinical trial sites—and accomplish more than 25% faster.

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Site Payments

We unburden sponsors and CROs from complex payment administration, while protecting data flow and preserving strong site relationships by ensuring timely, accurate site payments.

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Document Exchange

Securely expedite your document flow and tracking to help clinical trials start faster and smoother—and create an impeccable audit record.

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Connecting patients to clinical trials

We optimize recruitment and enrollment results by identifying and referring patient candidates to clinical sites or physician practices.

Enhancing site resources and capabilities

We streamline study processes by providing sites and practices the necessary resources for screening, enrolling, treating and retaining patients to meet program goals.

Improving study data quality

Our clinical experts and advanced technology mitigates the risks of bias, variability, and human error through centralized ratings, review and training.

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Find & Attract

Study Marketing

We reach patient populations efficiently via demographic, psychographic and geographic targeting, and build awareness with advertising, online marketing and social media.

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Enroll & Manage

Recruitment & Retention

Once likely study patients are identified, don’t risk shortfall: ensure you reach–and maintain–target enrollment uding our dedicated, highly efficient recruitment and retention specialists.

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Observe & Assess

Clinical Rater Assessment

Increase the accuracy of study results by ensuring consistent scoring of therapeutic effects and outcomes with our rigorous rater training and certification.

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Patient Identification

Jump start clinical study enrollment with more focused, cost-efficient chart review. Our dedicated team frees up your site staff, rapidly identifying qualified patients so your trial begins and stays on schedule.

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eConsent

Increase patient retention by engaging patients more effectively during the informed consent process. Our advanced educational techniques and electronic consent process also reduce costs and risk.

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Clinical Outcomes Assessment

Improve signal detection and minimize error rate in clinical trials by combining Virgil, our Electronic Clinical Outcomes Assessment platform, with our unmatched therapeutic measurement expertise.

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“The physician and I were confident that we had already identified all our patients but after having WCG ThreeWire complete the Chart Review service we were impressed by how many more patients were identified.”

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“We are establishing a culture of advancement in the industry, but also advancement in our individuals. It’s a company that’s committed to ensuring that our best employees are recognized and given the opportunities to advance. I’ve been given more opportunities in the past four years at ePharmaSolutions and WCG than I have in my prior 7-10 years of working.”

Brian Mundy
Director, Product Strategy at ePharmaSolutions

“The WCG Clinical Observation Assessment service’s tablet and digital scales improve our ability to administer quality assessments with expert reviews and the assurance of higher quality data.”

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Complete the form to schedule a consultation with WCG. We’ll share benchmark data from the WCG Knowledge Base, analyze your results, and share some of the common practices of top performers.

Benchmark your study enrollment performance versus your peers

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Patient Files

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Patient Identification

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Patient Recruitment

Bio Safety

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Institutions

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Learning Management

Product Contact

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Local IBCS

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Site Payments

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Study Marketing