[PRNewswire] Major Release of Veeva Site Connect
전체 맥락을 이해하기 위해서는 본문 보기를 권장합니다.
"By standardizing how information is shared across all sites in one application with Veeva Site Connect, we aim to save time and effort that can be focused on treating patients," said a clinical operations excellence leader at a top 20 biopharma. "Our goal is to eliminate manual handoffs and inefficiencies for faster site start-up, more efficient monitoring, and simplified study closeout."
"I would be ecstatic if all our sponsors use Veeva Site Connect. It gives sites a much more efficient way to collaborate with sponsors, maintain regulatory compliance, and get critical therapies to patients faster," said Alisha Garibaldi, CEO, Skylight Health Research. "The less time we spend doing administrative work in systems, the more time we have to execute trials and help patients."
이 글자크기로 변경됩니다.
(예시) 가장 빠른 뉴스가 있고 다양한 정보, 쌍방향 소통이 숨쉬는 다음뉴스를 만나보세요. 다음뉴스는 국내외 주요이슈와 실시간 속보, 문화생활 및 다양한 분야의 뉴스를 입체적으로 전달하고 있습니다.
-- It streamlines clinical trial execution for sites and sponsors
-- New capabilities and simple, standard site experience cut trial time and expense
-- Fixed price implementation to get up and running quickly
- Industry advances to connected trials as seven of the top 20 biopharmas adopt Veeva Site Connect
SEOUL, South Korea Sept 10, 2024 /PRNewswire=연합뉴스/ -- Veeva Systems[https://www.veeva.com/ ] (NYSE: VEEV) today announced, in a major step forward for clinical trial execution, the newest release of Veeva Site Connect[https://www.veeva.com/products/veeva-site-connect/ ], adding powerful new capabilities and a streamlined site-centric experience to simplify and standardize sponsor-site collaboration. With Veeva Site Connect, sponsors reduce the time and effort of site start-up, study conduct, and closeout for higher-quality trials at a significantly lower cost.
"By standardizing how information is shared across all sites in one application with Veeva Site Connect, we aim to save time and effort that can be focused on treating patients," said a clinical operations excellence leader at a top 20 biopharma. "Our goal is to eliminate manual handoffs and inefficiencies for faster site start-up, more efficient monitoring, and simplified study closeout."
To deliver better trial execution in less time, the expansion of Veeva Site Connect includes major application and implementation advances.
- New capabilities expand Site Connect beyond document exchange and safety distribution: Veeva Site Connect adds Study Communications, Contacts, Payment Information, and quick links to sponsor systems to already powerful Document Exchange and Safety Distribution capabilities.
- Optimized site user interface that's the same for all trials: Organizing everything sites need in an intuitive site homepage with simple sidebar navigation means sites can easily stay informed and close out tasks in just a few clicks. Having the same user experience for all trials gives sites a standard way to work across sponsors.
- Open for use by any site, anywhere: Veeva Site Connect is accessible for all sites everywhere. Sites that use Veeva SiteVault[https://sites.veeva.com/ ] as their eISF get the added benefit of connecting their study for seamless bidirectional document exchange.
- Simple fixed price implementation to get up and running in two to four months: With a standard fixed fee engagement of two to four months, depending upon company size, sponsors can make a big impact quickly toward their goal of faster, higher quality trial execution.
"I would be ecstatic if all our sponsors use Veeva Site Connect. It gives sites a much more efficient way to collaborate with sponsors, maintain regulatory compliance, and get critical therapies to patients faster," said Alisha Garibaldi, CEO, Skylight Health Research. "The less time we spend doing administrative work in systems, the more time we have to execute trials and help patients."
"By implementing Veeva Site Connect for our safety letter distribution process, we anticipate achieving a significant reduction in manual processing while enhancing oversight and compliance," said Marta Jureczko-Hinzmann, head of global clinical solution services at AstraZeneca. "Sharing safety letters across all sites globally within a single application will allow us to harmonize the entire process across the company and optimize how we allocate valuable resources."
Veeva Site Connect is part of Veeva Clinical Platform[https://www.veeva.com/products/veeva-clinical-platform/ ], the complete and connected solution supporting patients, sites, and sponsors. Veeva Site Connect plays a critical role as the industry moves to simplify and standardize site collaboration, and seven of the top 20 biopharmas have already adopted Veeva Site Connect to streamline trials.
See the Veeva Site Connect demo[https://www.veeva.com/resources/veeva-site-connect-demo/ ] and learn more at Veeva R&D and Quality Summit[https://www.veeva.com/kr/events/korea-summit/ ] October 15 in Korea, where top biopharmas will share how they use Veeva Site Connect to simplify trial execution for greater quality and speed.
Additional Information
For more on Veeva Site Connect, visit: veeva.com/VeevaSiteConnect
Connect with Veeva on LinkedIn: linkedin.com/company/veeva-systems
About Veeva Systems
Veeva is the global leader in cloud software for the life sciences industry. Committed to innovation, product excellence, and customer success, Veeva serves more than 1,000 customers, ranging from the world's largest biopharmaceutical companies to emerging biotechs. As a Public Benefit Corporation[https://www.veeva.com/pbc/ ], Veeva is committed to balancing the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves. For more information, visit veeva.com.
Veeva Forward-looking Statements
This release contains forward-looking statements regarding Veeva's products and services and the expected results or benefits from use of our products and services. These statements are based on our current expectations. Actual results could differ materially from those provided in this release and we have no obligation to update such statements. There are numerous risks that have the potential to negatively impact our results, including the risks and uncertainties disclosed in our filing on Form 10-Q for the period ended July 31, 2024 and in our subsequent SEC filings, which you can access at sec.gov.
Source: Veeva Systems
[편집자 주] 이 보도자료는 자료 제공사에서 제공한 것으로, 연합뉴스는 내용에 대해 어떠한 편집도 하지 않았으며, 연합뉴스의 편집방향과는 무관함을 밝혀 드립니다.
(끝)
출처 : PRNewswire 보도자료
Copyright © 연합뉴스 보도자료. 무단전재 및 재배포 금지.
- [수능] EBS·입시업계 "국어, 킬러문항 없었다…작년 수능보다 쉬워"(종합) | 연합뉴스
- 尹대통령, APEC·G20 참석차 출국…한동훈 환송(종합) | 연합뉴스
- 李, 김혜경 재판에 "먼지털기 희생제물…죽고싶을 만큼 미안" | 연합뉴스
- '3억으로 100억 사업' 막는다…부동산PF 자기자본 20%로 상향 유도(종합) | 연합뉴스
- 트럼프, 다시 김정은과 협상할까…재소환되는 '하노이 노딜'(종합) | 연합뉴스
- 외환당국 7개월만에 구두개입…"과도한 변동성에 적극 조치"(종합) | 연합뉴스
- [수능] 수험생 태워주고 수험표 찾아주고…경찰 187건 지원 | 연합뉴스
- 美대선 후 첨단산업 패권경쟁 향방은…오늘 연합뉴스 미래경제포럼 | 연합뉴스
- 정부, 북한군 전투 참여에 "침착·절제 원칙으로 단계적 대응" | 연합뉴스
- 이재명 선거법 위반 내일 1심 선고…'사법리스크' 첫 시험대 | 연합뉴스