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- Просмотров 15 479
Reed Tech Life Sciences
США
Добавлен 13 ноя 2013
Life Sciences Solutions Driven by Accuracy and Insight
Reed Tech offers product and service solutions to help Life Sciences professionals gain control over their own and their industry's data. Our offerings smooth the collection, transformation, submission and analysis of regulatory data for manufacturers and distributors of medical device and drug products, and for those who support them in consulting and IT roles.
Reed Tech offers product and service solutions to help Life Sciences professionals gain control over their own and their industry's data. Our offerings smooth the collection, transformation, submission and analysis of regulatory data for manufacturers and distributors of medical device and drug products, and for those who support them in consulting and IT roles.
Catch Up with LexisNexis Reed Tech: MoCRA Regulations Update
With FDA enforcement of MoCRA Product and Facility listings beginning on July 1, 2024, Reed Tech subject-matter experts, Gary Saner and Patti Shragher, are here to provide industry with the newest update.
Просмотров: 40
Видео
Ask the Experts Part II-QMS for MDR/IVDR and nonconformities, special scenarios
Просмотров 582 месяца назад
Reed Tech hosted industry panelists, Dr. Bassil Akra of AKRA TEAM and Lisa Van Ran at Greenlight Guru. EUDAMED MDR/IVDR considerations for QMS were discussed with best practices and insights.
What are companies saying about LexisNexis Reed Tech?
Просмотров 62 месяца назад
A few recent comments from customers of Reed Tech. We serve manufacturers and distributors of medical devices and drug products, and those who support them in consulting and IT roles by delivering better outcomes for the collection, transformation, submission and analysis of regulatory data. Our solutions support the innovation ecosystem and enable you to achieve regulatory compliance and impro...
Reed Tech Insights Part I IVDR Proposal and EUDAMED rollout
Просмотров 534 месяца назад
Hear the latest on the EC proposal and possible scenarios / timelines affecting IVDR UDI submissions.
Reed Tech Insights Part II EUDAMED Timeline Scenarios and Member State Adoption
Просмотров 464 месяца назад
Hear the latest update on the EC proposal concerning EUDAMED adoption of the six modules plus member state updates.
Reed Tech and Net Promoter Score Comments
Просмотров 185 месяцев назад
Customers give Reed Tech 'world-class' ratings for value and services provided for regulatory compliance submissions to global health authorities. Contact us to learn more about how Reed Tech can become an 'extension' of your team, freeing up your time for other priorities. email: Pharma@ReedTech.com or MedDevice@ReedTech.com
RTLS 2023 Holiday video short
Просмотров 106 месяцев назад
Reed Tech Coffee Talk: eCTD for Small Pharma Companies
Просмотров 196 месяцев назад
Learn from our Pharma Professional Services team how we can support the regulatory teams at small Pharma companies.
Reed Tech Insights-Intro to eCTD (Electronic Common Technical Document) Part II
Просмотров 377 месяцев назад
Gain an understanding of the illustrative 'pyramid' of components comprising an eCTD from the experts at Reed Tech. Contact us to learn more: email us at Pharma@ReedTech.com or call 1-215-557-3010
Reed Tech Insights-Intro to eCTD (Electronic Common Technical Document) Part I
Просмотров 337 месяцев назад
Learn about the background of eCTD and how it has streamlined Drug Marketing Applications to global Health Authorities. Questions about eCTD? Contact us: Pharma@ReedTech.com or call 1-215-557-3010
Reed Tech Insights -- Basic UDI GS1 Implementation Example
Просмотров 617 месяцев назад
See an example of a EUDAMED Basic UDI-DI implemented per GS1 standard. Basic UDI-DI must be assigned by May 26, 2024 in order to engage with a Notified Body. If you have questions about EUDAMED UDI data submissions, don't hesitate to contact us. Email: MedDevice@ReedTech.com
Reed Tech Insights -- Intro to EUDAMED Basic UDI DI
Просмотров 727 месяцев назад
Get a definition of EUDAMED Basic UDI-DI and how it is different from EUDAMED ID. Questions about medical device UDI submissions to health authorities? Contact us: MedDevice@ReedTech.com
Reed Tech Insights-OTC Monograph Regulations Part II
Просмотров 118 месяцев назад
Hear a quick review of changes coming into play in 2023 due to the OTC Monograph regulation, affecting makers of some OTC cosmetic related products. If you have questions about US FDA data submissions, drug listings or establishment registrations, get in touch with Reed Tech. email us: Pharma@ReedTech.com
Reed Tech Insights--Intro to OTC Monograph Regulations Part I
Просмотров 198 месяцев назад
Learn about US FDA OTC Monograph Regulations affecting companies involved with OTC drug products. Some changes are taking effect in 2023. Questions? Contact the experts at Reed Tech: Pharma@ReedTech.com
Reed Tech Insights Intro to Modernization of Cosmetics Regulation Act of 2022 (MoCRA)
Просмотров 508 месяцев назад
Hear a quick introduction into the topic of MoCRA what is it, who is affected, what cosmetic makers should consider concerning product facility and product listings to FDA. Thanks to Reed Tech (Caitlyn Lynes) and Garg Law (Shelly Garg) for taking us through the basics.