inVentiv Health says it will now offer a one-stop-shop for pharma and biotech training services after merging its subsidiaries Pharmaceutical Institute and Preceptiv Learning Solutions.
Europe’s Innovative Medicines Initiative (IMI) has adopted the Clinical Data Interchange Standards Consortium’s (CDISC) standards for all future projects in a move announced this week.
The EU Clinical Trials Register (EU-CTR) has been formally recognised by the World Health Organization (WHO) as one of the primary registries for its International Clinical Trials Registry Platform (ICTRP).
Kellman Pharmaceutical Services (KPS) and trial management services firm Y-Prime have put pen to paper in a deal to develop a series of clinical electronic monitor visit reporting (e-MVR) tools.
AmerisourceBergen has bought informatics firm IntrinsiQ for $35m (€25m) continuing the spending spree it began earlier this week with the acquisition of market access consultancy Premier Source.
Outsourcing-Pharma presents a round-up of CRO M&A, including inVentiv closing the PharmaNet deal, Icon adding technology, and Bracket inking its first takeover.
US contract research organisation (CRO) PRA International claims it intends to “reshape how the industry manages trials” after acquiring Indian eClinical software developer, Kinship Technologies, for an undisclosed amount.
Phlexglobal, a contract research organisation (CRO) specialising in trial master file (TMF) and eTMF management, has expanded its US operations with the opening of an office in Philadelphia, Pennsylvania.
Algorithmic Research (ARX), the digital signature specialist, has released a short video to highlight the benefits of using digital signature technology in clinical environments.
Perceptive Informatics, an eClinical solutions provider, has announced the results of a survey to find out what the biopharma industry considers the most important eClinical attributes.
BioClinica grew service revenues in the fourth quarter and predicted the trend will continue in 2011 when it will “eliminate certain duplicate functions”.
Passwords used to protect personal health information in Canadian clinical trials are often too easy to crack, according to a report in the Journal of Medical Internet Research (JMIR).
The FDA has issued guidance on electronic data in clinical trials to help eliminate duplication, reduce transcription errors and promote real-time entry.
PRO Consulting has expanded its range of Patient Reported Outcomes (PRO) offerings to better support drug and medical device developers using PROs in all stages of their clinical development programs.
PharmaNet has launched its Initiator data capture and PKS analysis platforms in a bid to speed up data acquisition and processing of Phase I trial reports.
Clinical software developer, Forte Research Systems, has opened a new office in Bangalore, India, to take advantage of growth in the clinical research industry on the sub-continent.
BioClinica’s Optimiser software has bagged the firm a new five-year deal with a “top-ten” pharma company which intends to use the tool for all its clinical trial operations.
BioClinica is launching its new Trident IVR/IWR platform, to provide a cheaper, quicker way to set up, monitor and maintain randomisation and supplies in clinical trials.
Oracle Health Sciences has strengthened its clinical trial analytics offering to reduce start up times and offer greater insight into screening, recruitment and retention.
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