Consent Vault

Main Menu
Schedule a Demo
  • All
  • AI in Medicine
  • Archived
  • Clinical Trials
  • News
  • Patient Rights
  • Real-World Data

News

AI in Medicine, News / By

New Patent – Permission Monitoring and Data Exchange

Consent Vault, Inc receives issuance of a patient for a groundbreaking AI- and machine learning–enabled consent management system designed to accelerate data-driven insights, data enablement and governance.  The current application of this patented technology empowers patients to define how their clinical, genomic, and real-world data may be used—specifying access by data type, purpose, authorized parties, […]

New Patent – Permission Monitoring and Data Exchange Read More »

doctor, patient, consultation-5710152.jpg
Clinical Trials, News / By

Minimizing $50-60B loss in annual failed Cancer Clinical Trials by Optimizing Patient Identification and Recruitment Strategies

Clinical trials are crucial in the development of new cancer treatments, but the staggering loss of $50-$60 billion annually due to failed oncology clinical trials emphasizes the need for improved oncology patient identification and recruitment strategies. A recent review found patient participation in oncology trials to be low, ranging from 2% to 8% of adult

Minimizing $50-60B loss in annual failed Cancer Clinical Trials by Optimizing Patient Identification and Recruitment Strategies Read More »

dna, evolution, technology-3778336.jpg
News / By

Florida imposes criminal sanctions for violation of certain health privacy rights

Florida imposes criminal sanctions for violation of certain health privacy rights Florida took data and health privacy rights a step further and passed HB 833 the Protecting DNA Privacy Act which went into effect October 1, 2021, which “establishes new criminal offenses applicable to persons” in violation of HB 833. This new law is designed to  a) extend

Florida imposes criminal sanctions for violation of certain health privacy rights Read More »

research, virus, corona-5297028.jpg
News / By

Tissue and DNA material used without informed consent and authorization leads to lawsuits

Tissue and DNA material used without informed consent and authorization leads to lawsuits On the 70th anniversary of the death of Henrietta Lacks, her family has filed a lawsuit on October 4, 2021, against Thermo Fisher Scientific for using cells taken from Henrietta Lacks while a patient at Johns Hopkins Hospital in Baltimore without her

Tissue and DNA material used without informed consent and authorization leads to lawsuits Read More »

News, Patient Rights / By

Implications of Informed Consent: Lessons Learned from Henrietta Lacks on Patient Rights, Medical Ethics, Transparency and Research

The story of Henrietta Lacks first came to light in the early 1970s, long after her cells were taken without her knowledge or consent. The first public mention of Henrietta Lacks and her cells was in a 1976 article

Implications of Informed Consent: Lessons Learned from Henrietta Lacks on Patient Rights, Medical Ethics, Transparency and Research Read More »

Scroll to Top