News

ACRP and CenterWatch released a collaborative benchmarking report on clinical research site performance

With numerous strategic partnerships underway, X-Chem emerges as a leading biotechnology company focused on drug discovery

Radiant Research/Clinical Research Advantage has completed enrollment for the Dynavax Technologies Corporation phase III clinical trial

Effective leadership is needed in a trial leader, but what exactly does that entail?

Thomas Krohn, Director of Clinical Open Innovation at Eli Lilly, showcased a breakthrough study design platform and process that study teams are currently utilizing.

Medical imaging is an important source of subject eligibility, drug efficacy, and safety data for many clinical trials.

Key differences and gaps in requirements for testing and documenting product similarity have emerged among the European Union, the US and other regions.

New addition expands WCG's eClinical offerings for improving clinical trial start-up and management

PHT Corporation announced its LogPad System has been selected by Agile Therapeutics for use

OpenClinica announces that University of Maryland School of Medicine has selected the OpenClinica Enterprise Edition for the Ultra Registry

The University of Maryland School of Medicine uses OpenClinica's EDC platform to support their multi-center aneurysm trial.

WIRB-Copernicus Group announced that ePharmaSolutions has joined its group of companies.

eDiary System selected to promote data quality and clinical trial efficiencies

What can be gleaned about the direction that health policy will take for the next five years under the new European Commission, scheduled to take office at the beginning of November?

President and Co-founder of Canadian CRO Scimega Research, Denise Deakin, addresses last week's article published in the Toronto Star

Cloud technology is enabling more clinical trial sponsors to meet health authorities' increasing demands for trial master file accessibility and completeness.

Timely completion of clinical trials is the weak link in the drug development process, and there is no shortage of suggestions for how to improve it.

ClinicalTrials.gov

The US FDA, in open meetings, stated the Thorough QT trial "must" be replaced.

Inevitably, the conversation consistently comes back to a simple philosophical debate?should software solutions be configurable or customizable?

WIRB-Copernicus Group announced that its Western Institutional Review Board has been reaccredited

Reaccreditation underscores WIRB-Copernicus Group's commitment to enhancing safeguards for clinical trial participants

Veeva Systems announced updated results of a large TMF survey

Cloud technology enables clinical trial sponsors to meet health authorities' increasing rigor for trial master file accessibility and completeness

A Polish legal expert and the German/Canadian President of the European Federation of Pharmaceutical Industries and Associations will be the co-chairs of the next Drug Information Association EuroMeeting.

The current regulatory system for medicines in Europe could be used in a more efficient and effective manner, according to a report from Escher.

A new report from Escher, the independent TI Pharma platform for regulatory innovation, shows that the current regulatory system for medicines in Europe can be used in a more efficient and effective manner.

AAHRPP announced that it has accredited three more organizations.

The Association for the Accreditation of Human Research Protection Programs today announced that it has accredited three more organizations

There are various estimates in the public domain that applying big data strategies could potentially generate up to $100 billion in value annually across the US healthcare systems.