Refine by
Safety Testing Articles & Analysis: Older
35 news found
The process of antipsychiatric drug development typically involves several stages, including identifying potential drug targets, conducting preclinical research to test the safety and efficacy of potential drug candidates, and then moving on to clinical trials to further evaluate the drug’s effectiveness and safety in human subjects. ...
The company now offers a comprehensive portfolio of Patulin Test Reagents for food safety applications, including Patulin ELISA Kit, Patulin Standard (95%), and Anti-Patulin Polyclonal Antibody. ...
The new service offerings include medical device safety testing, biocompatibility testing, validation and verification, and reusable medical device testing. ...
We are thrilled to announce that Vantage, has successfully passed NHS England’s rigorous LFPSE (Learning from Patient Safety Events) compliance testing and are officially recognised as an accredited LFPSE supplier. This accreditation is a testament to our commitment to enhancing patient safety in healthcare organisations across the nation. ...
” “These exciting results provides further confidence in the Oligomerix approach as we prepare to enter clinical testing next year,” said Bill Erhardt, M.D., Chief Medical Officer of Oligomerix. ...
The company announced plans to begin clinical testing of ASC618 in hemophilia A patients last year, after the FDA gave the green light for such trials. ...
In addition, the Logica-C offering will use the advanceable leads and trained predictive models to rapidly progress the program, ultimately aiming to deliver a development candidate that has undergone necessary safety and efficacy tests and is ready for IND-enabling studies. Logica utilizes industry-leading predictive models, chemical design and synthesis ...
Occupational asthma is triggered by an exposure on the job and the National Institute for Occupational Safety and Health (NIOSH) states that there are over 300 known, or suspected, substances in the workplace that can cause or worsen asthma. ...
Participants’ response to treatment will be assessed via parent, and teacher rating scales, as well as cognitive tests. A subgroup of approximately 58 children will receive functional magnetic resonance imaging (fMRI) at baseline and after four weeks of therapy. ...
Kurin, Inc., the inventor and manufacturer of the Kurin® blood culture collection sets announced that they have commenced the commercial launch of their push-button needle, to be used as part of Kurin blood culture sets. The Advance Safety Needle System was tested in 2021 and is now being sold into accounts using Kurin. “We are proud to commercialize ...
Cosmetic manufacturers have legal responsibility for the safety and labeling of their products. However, FDA can and does take action on cosmetics that are not in compliance with the law on the market. ...
Many patients are reluctant to visit surgeries and extensive testing causing severe backlogs across laboratories, POC devices provide the first step in the diagnostics pathway, supported by further lab or clinical evaluation, if required. ...
This early feasibility study (EFS) of the device will begin later this year at Mount Sinai Hospital, New York, and will assess the safety and efficacy in patients with severe paralysis. Outcomes will include the use of the brain data to control digital devices and achieve improvements in functional independence. ...
By providing support and intellectual property that enables both non-profit and for-profit entities to develop CRISPR-based diagnostic testing, The 221b Foundation seeks to aid in the fight against the global COVID-19 pandemic while furthering access and diversity in STEM industries. Led by industry experts in the fields of diagnostic testing, STEM and diversity, ...
The CMC SME : a key role to acceptance and patient safety Enter the Chemistry, Manufacturing and Controls Subject Matter Expert (CMC SME) for the purpose of technical oversight. ...
“By providing our CRISPR technology to these test developers, the critical need for improved testing during the pandemic will be further satisfied, improving healthcare at a global ...
The candidate generated strong immune responses in animal models and was approved for combined phase 1 and 2 clinical trials by the South Korean Ministry of Food and Drug Safety in January. The first phase will include 50 healthy Korean adults and tests for safety, tolerance and immune response. The second phase will include 230 adults and ...
INOVIO and CEPI are committed to making a vaccine available as soon as possible for emergency use as a stockpile product post-Phase 2 testing. Dr. J. Joseph Kim, President and CEO of INOVIO, said, "We have observed that INO-4500 vaccination generates robust antibody and T cell immune responses in a Phase 1 clinical trial conducted in the U.S., and this continued advancement of ...
” The goal of this project is to prepare for and then conduct a First-In-Human pilot clinical trial that will test the safety of Cytex’s innovative hip implant. Cytex is grateful for the ongoing support of the NIH. ...
” The goal of this project is to prepare for and then conduct a First-In-Human pilot clinical trial that will test the safety of Cytex’s innovative hip implant. Cytex is grateful for the ongoing support of the NIH. ...