Fri.Apr 03, 2020

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Hybrid DCTs Reduce Dropout Rates in Long-Term Studies

VirTrial

Clinical studies are carefully designed to address the unique needs of not only the sponsor, but more importantly, the patients that commit to participate. Depending on the nature and severity of the condition, study lengths vary. A cardiovascular outcome trial (CVOT), for example, requires a long duration (potentially up to five years) in order to effectively evaluate real-life, long-term outcomes.

Trials 98
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PharmacyChecker Online Pharmacy Authentication Role Recognized in OECD/EU Report on Counterfeit Drugs

Pharmacy Checkers

When I read fancy-looking international reports that address the problem of counterfeit drugs, too seldom is our work recognized in verifying international online pharmacies in a manner that saves the lives of consumers looking online for affordable medicine. To some extent, that’s because the global pharmaceutical industry is often a major data source for these reports.

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Client-Pharma FAQs During the COVID-19 Crisis

Client Pharma

Here at Client-Pharma, we wanted to assure our clients, partners and contacts that we are continuing to maintain our high level of customer service throughout our business during the global pandemic. Please find below some FAQs addressed by Andrea Chopek , President North America at Client-Pharma, Inc. If you have any specific queries, please contact us via our normal channels – phone and email: Q: Is Client-Pharma contactable?

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Client-Pharma FAQs During the COVID-19 Crisis

Client Pharma

Here at Client-Pharma, we wanted to assure our clients, partners and contacts that we are continuing to maintain our high level of customer service throughout our business during the global pandemic. Please find below some FAQs addressed by Andrea Chopek , President North America at Client-Pharma, Inc. If you have any specific queries, please contact us via our normal channels – phone and email: Q: Is Client-Pharma contactable?

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The New Age of Decentralized Clinical Trials

White paper that delves into the complex topic of Decentralized Clinical Trials and how to master them within the confines of FDA Regulations