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Taste Testers FAQs
New Testers | Current Testers | Driving Directions | Test Day Tips | Taste Testers FAQs | Contact Information Taste Testers FAQs How do I sign up to participate? Sign up here and provide your contact information. All of your information is confidential. Covance and The National Food Lab never provides or sells any personal taste tester information to outside parties. How often can I participate? Most testers will be able to participate several times per year. If you’ve already...
SEND Solutions - Standard for the Exchange of Nonclinical Data | Covance
The SEND countdown to December 17, 2016 has begun. Your move to SEND doesn’t have to be stressful – we can help.
SEND Solutions - Standard for the Exchange of Nonclinical Data | Covance
The SEND countdown to December 17, 2016 has begun. Your move to SEND doesn’t have to be stressful – we can help.
SEND - What to Expect
The Standard for the Exchange of Nonclinical Data (SEND) is the FDA's new nonclinical submission requirement that goes into effect in December of 2016. The webinar guides you, step by step, through a practical and proactive look at using a SEND dataset and walking through a typical SEND experience: receiving a file, opening and viewing your dataset and saving to spreadsheet format. Also discussed are the domains of a SEND dataset and the ways that the FDA may view your data, along with...
Begin With the SEND in Mind: Challenges, Learnings and Opportunities
During this webinar, you will receive a brief review of SEND, Understanding Compliance, Data Integration and Multi-Site Studies, Logistics and Uses and what's next for SEND.
SEND Sell Sheet
SEND Sell Sheet
Are You SEND Ready? Preparing for SEND Implementation and Its Resulting Benefits
Learn how to handle and interpret datasets for the FDA requirement for SEND (Standard for the Exchange of Nonclinical Data).
The Tale of a Real-life SEND Test Submission
What to Expect When Submitting Your First SEND Dataset to the FDA. With the December 17, 2016* requirement for the FDA Standard for the Exchange of Nonclinical Data (SEND*) fast-approaching, our Covance SEND action team prepared a dataset for test submission to the FDA. This helped us to better understand the FDA's SEND submission requirements, build experience and confirm our readiness to help clients submit their SEND datasets.
Overcoming Data Integration Challenges to Produce SEND Datasets
ACT 2016 -- Nonclinical toxicology studies that include phases run at multiple test sites (aka multi-site studies) are commonplace in the industry and can involve one or more organizations. With the FDA requirement for including SEND (Standard for Exchange of Nonclinical Data) datasets in NDA submissions taking effect on 17 Dec 2016, integrating data generated from the test facility and multiple test sites into one submission-ready and compliant SEND dataset is challenging. Covance...
SEND is Here. Are you Ready for Data-Driven Decision Making?
There's no denying that studies are only as strong as their resulting data-and nonclinical studies produce a lot of data.
PowerPoint Presentation
The FDA requires nonclinical data in all submissions for carcinogenicity and general toxicology studies initiated after December 17, 2016, to comply with data standards specifications. Learn more about the new SEND regulatory requirements and how Covance can help you get SEND-ready.
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Search Filters Showing results 1 - 16 of 36 for send. Showing results 1 - 16 of 36 for send. Taste Testers FAQs New Testers | Current Testers | Driving Directions | Test Day Tips | Taste Testers FAQs | Contact Information Taste Testers FAQs How do I sign up to participate? Sign up here and provide your contact information. All of your information is confidential. Covance and The National Food Lab never provides or sells any personal taste tester information to outside...
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Contract Research Organization (CRO) | Clinical Trials | Covance
Covance, a global contract research organization and drug development services company, has helped bring 49 of the top 50 best-selling drugs to market.
General Toxicology Studies | Safety Assessment | Covance
As the world's largest GLP tox enterprise, gain insights with Covance general toxicology studies quickly so you can advance your best drug prospects.
Global CRO Drug Development Services | Covance
Covance, a top global CRO, partners with you for each stage in drug evaluation and development life cycle, from research to commercialization.