news roundup
Clinical Ink, the pioneering provider of eSource and next-generation ePRO/eCOA solutions for clinical development, announced that the private equity team at NovaQuest has acquired a majority of the outstanding shares of the company from existing investors and provided a substantial infusion of additional growth capital.
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Driving Product Development and Finding the Fast Track in Early-Phase Oncology Programs
Tuesday, June 19, 2018 at 11am EDT | 10am CDT | 4pm BST | 5pm CEST Register now |
WIRB-Copernicus Group (WCG) Clinical Services Division, a provider of solutions that improve the quality and efficiency of clinical research, announced the opening of the company's new office in Tokyo, Japan which will allow them to provide global clinical trials.
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Is RBM living up to the hype? The state of RBM in clinical development
Wednesday, June 13, 2018 at 11am EDT Register now |
Saama Technologies, a clinical and health data analytics company, and ICON plc, a global provider of drug development and commercialization solutions and services, have partnered to accelerate the use of Real World Evidence across the product lifecycle and drive mission critical decisions for medical affairs, reimbursement, and commercialization functions.
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The Future of ECOA
Tuesday, June 12, 2018 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Register now |
Peter O'Donnell explores potential parallels of the U.S. "right-to-try" debate in Europe.
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Functional Service Models Reimagined: Integrating services and innovation for accelerated clinical development
Wednesday, June 6, 2018 at 11am EDT Register now |
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Design of Early Phase Clinical Trials: How to Increase Efficiency and Probability of Success?
Europe: Tuesday, June 5, 2018 at 3pm CEST | 2pm BST
North America: Thursday, June 14, 2018 at 11am EDT | 10am CDT | 8am PDT
Register now |
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Protein Biotherapeutic BioAnalysis, by Immunoaffinity LC-MS: Latest Trends and Recommendations
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Articles
From 2019, to comply with requirements for greater transparency around clinical research as part of the EU Clinical Trials Regulation 536/2014, life sciences firms will be expected to prepare plain-language summaries for all Phase I through IV interventional trials, which can be understood by patients, the general public, and experts.
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Considerations when Addressing the Challenges of Time, Cost, and Data Standardization in Clinical Trials
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When less is more. Using three referral labs vs. one central lab.
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Blog Posts
The biopharmaceutical industry continues to explore how mHealth can change clinical trials, as the discussion continued at Hanson Wade's mHealth for Clinical Trials EU Summit in London.
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Operationalizing Gene Therapy Trials
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With the rise in gene therapies entering clinical trials, it is important to address the operational challenges associated with these types of trials.
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