Remo CRO

News

Unlocking the Value of Ethics in Clinical Research

04.29 2017.

Although the quest for profit is understandable, research site leaders who are looking to fill their clinical trials would do well to first be sure their organizations are viewed as trustworthy, says Marcy J. Maslov, CPA, CGMA, MBA, founder and CEO of Empowerment Unlimited Coaching, LLC. “Positive ethical culture reduces turnover, builds loyalty, saves money, […] Details

Navigating the Clinical Trials Regulatory Landscape in the European Union

04.29 2017.

With a new Regulation on clinical trials coming into full effect in the European Union (EU) by October 2018, U.S.-based sponsors can expect a greater degree of harmonization across the countries in the EU, especially in terms of review, approval, and reporting, says Jo Burmester, BSc, director of global operations with PharmaSchool Ltd. “There will […] Details

ACRP, Barnett Announce Training Partnership

04.28 2017.

The Association of Clinical Research Professionals (ACRP) and Barnett International (Barnett) today announced the formation of a strategic partnership to provide ACRP’s 13,000-plus global members with expanded access to high-quality education and training programs through Barnett. As a result of the partnership, ACRP members have immediate, exclusive access at a reduced rate to Barnett’s curriculum, […] Details

Synexus, Radiant Research to integrate operations

04.28 2017.

European-headquartered Synexus and U.S.-based Radiant Research announced a full operational integration to form a single global site network of 185 sites with 1,500 employees. This move will create the world’s largest site network, spanning 11 countries and offering access to more than 100 million patients in key clinical development markets, operating under the Synexus name. […] Details

Quorum Review IRB launches IRB-integrated eConsent solution

04.28 2017.

Quorum Review IRB is launching a cloud-based and secure electronic informed consent (eConsent) solution that simplifies research studies, accelerates study startup and improves participant engagement. Developed by Kinetiq, the technology and consulting division of Quorum, Q Consent is the first and only IRB-integrated eConsent solution. “Our mission at Quorum is to move research forward together, and our Q Consent […] Details

CytRx Announces FDA Agreement on Regulatory Pathway to Approval for Aldoxorubicin in Soft Tissue Sarcomas

04.27 2017.

LOS ANGELES, April 19, 2017 /PRNewswire/ — CytRx Corporation (NASDAQ: CYTR) today announced the U.S. Food and Drug Administration (FDA) has reached an agreement with CytRx on preparations for a New Drug Application (NDA) submission for… Details