Source: SCRIP CITELINE COMMERCIAL Jeeva’s founder and CEO talks to Scrip about how the firm’s clinical trial management platform does away with the need for
Source: Dermatology Times Gender gaps, with consistent underrepresentation of females, present a substantial challenge in clinical research.(1) Achieving a balanced representation of both genders has
Source: Pharmacy Times Gender gaps, with consistent underrepresentation of females, present a substantial challenge in clinical research.1 Achieving a balanced representation of both genders has
Source: Cision PRweb The FDA has released new guidance for decentralized clinical trials (DCTs) for drugs, biological products, and medical devices to improve DCT implementation.
Remote informed consent for a 14-site biospecimen collection study by a US brain disorders research consortium The client is a non-profit consortium led by 25+
Clinical trials are the long and complex process by which biopharmaceutical companies must prove the safety and efficacy of investigational new therapies to FDA before
Source: Nashville Medical News Between logistical burdens, distrust in the healthcare system, and lack of awareness and information in many non-English languages, key demographic groups
Source: Yahoo Finance MARKET INSIGHTS The virtual clinical trials market is one of the innovative approaches for traditional clinical trials, through remote monitoring and more
Source: ReportLinker Summary The global virtual clinical trials market is expected to grow at a CAGR of 17.59% during 2022-2027. MARKET INSIGHTS The virtual clinical
Patient recruitment is a major barrier in clinical trials. This involves the identification of patients, screening them for inclusion/exclusion criteria of a given clinical trial,
Jeeva Clinical Trials Inc.
