Report Reveals 70% of Medtechs Use Manual Processes for Managing Content and Claims
Report Reveals 70% of Medtechs Use Manual Processes for Managing Content and Claims
Reducing content approvals from more than four weeks and automating claims are key opportunities to drive speed to market
縮短內容審批時間,從四周以上減少到更短,同時自動化索賠是加快市場速度的關鍵機會
BARCELONA, Spain, Nov. 21, 2024 /PRNewswire/ -- Veeva Systems (NYSE: VEEV) today announced findings from the 2024 Veeva MedTech Commercial Benchmark survey revealing nearly 70% of medtech organizations rely on manual processes and homegrown applications to manage commercial content and claims. Without a purpose-built content management system, medtech commercial teams face go-to-market delays and growing compliance risk.
西班牙巴塞羅那,2024年11月21日 /PRNewswire/ -- veeva systems(紐交所:VEEV)今天公佈了2024年veeva MedTech商業基準調查的結果,顯示近70%的醫療科技組織依賴手動流程和自制應用程序來管理商業內容和索賠。沒有專門構建的內容管理系統,醫療科技商業團隊面臨市場推出延遲和日益增長的合規風險。
Despite the importance of connecting claims, evidence, and promotional materials, only 15% of organizations have streamlined processes with a central data repository where claims are directly linked to substantiation. The data shows there is significant opportunity for improvement across commercial content and claims management to gain visibility and speed.
儘管連接索賠、證據和促銷材料的重要性不容忽視,但只有15%的組織已經簡化流程,並建立了中央數據倉庫,索賠與證明直接相關。數據顯示,商業內容和索賠管理在提高可見性和速度方面有顯著的改善機會。
The benchmark survey of over 130 commercial medtech leaders found that:
對130多位商業醫療科技領導者的基準調查發現:
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Content personalization is a growing focus. More than 80% are pursuing strategies to tailor and specify messaging. Achieving compliant personalization at scale without the right systems remains a challenge amid strict regulatory requirements.
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Digital asset management (DAM) not yet in place for true omnichannel. Nearly 40% of organizations report not having a DAM system in place, limiting the management of personalizing content. Among those with a DAM, only 31% report having it accessible across marketing.
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Prolonged approval times result in missed opportunities. 60% of medtech companies using manual processes or homegrown solutions experience approvals taking more than four weeks. Marketing assets undergo an average of three to five rounds of reviews which can delay campaign launches, affecting product awareness and sales momentum.
- AI and automation of content continues to influence medtech. 45% of medtech organizations feel the most significant area AI can contribute is content creation.
- 內容個性化是一個日益關注的重點。超過80%的企業正在追求定製和具體化信息的策略。在嚴格的法規要求下,實現合規個性化大規模仍然是一個挑戰。
- 數字資產管理(DAM)尚未到位,無法實現真正的全渠道。將近40%的組織報告沒有建立DAM系統,限制了個性化內容的管理。在擁有DAM的組織中,只有31%報告能夠在市場營銷中訪問。
- 漫長的審批時間導致錯失機會。60%的醫療科技公司使用手動流程或自制解決方案,審批時間超過四周。營銷資產平均經歷三到五輪審查,這可能延遲活動發佈,影響產品知名度和銷售勢頭。
- 人工智能和內容自動化繼續影響醫療科技。45%的醫療科技組織認爲,人工智能能貢獻的最重要領域是內容創作。
"As the demand grows for more personalized promotional materials, medtech companies face scale and compliance challenges to adhere to regulatory standards and accurately reflect product efficacy and safety," said Jeff Gorski, senior director of commercial content strategy, Veeva MedTech. "This report shows that nearly every medtech organization has an opportunity to improve content and claims management processes for greater speed to market, compliance, and efficiency."
「隨着對個性化宣傳材料需求的增長,醫療科技公司面臨規模和合規挑戰,以遵守監管標準並準確反映產品的有效性和安全性,」 veeva systems商業內容策略高級董事Jeff Gorski表示。「這份報告顯示,幾乎每個醫療科技組織都有機會改善內容和聲明管理流程,以更快地上市、符合規定和提高效率。」
The 2024 Veeva MedTech Commercial Benchmark survey examines the current processes, challenges, and future opportunities for improvement in managing promotional content and claims.
2024年veeva systems醫療科技商業基準調查研究了當前管理宣傳內容和聲明的過程、挑戰及未來改進的機會。
Additional Information
For more on Veeva Vault PromoMats for MedTech, visit: veeva.com/medtech/PromoMats
Connect with Veeva on LinkedIn:
補充信息
有關醫療科技的veeva Vault PromoMats的更多信息,請訪問:veeva.com/medtech/PromoMats
在LinkedIn上與veeva systems聯繫:
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, 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/eu.
Veeva Systems Inc.
Veeva是全球領先的生命科學業雲端軟件。致力於創新、產品卓越和客戶成功,Veeva爲1000多個客戶提供服務,包括全球最大的生物製藥公司和新興生物技術公司。作爲公共利益公司,Veeva致力於平衡所有利益相關者的利益,包括客戶、員工、股東和服務的行業。欲了解更多信息,請訪問veeva.com/eu。
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, which you can find here (a summary of risks which may impact our business can be found on pages 36 and 37), and in our subsequent SEC filings, which you can access at sec.gov.
Veeva前瞻性聲明
本發佈包含有關veeva公司產品和服務以及使用我們產品和服務的預期結果或效益的前瞻性聲明。這些聲明基於我們目前的期望。實際結果可能與本發佈中提供的結果有實質不同,我們沒有義務更新這些聲明。存在許多風險可能對我們的結果產生負面影響,包括我們在2024年7月31日結束的10-Q表格中披露的風險和不確定性(您可以在這裏找到關於可能影響我們業務的風險的摘要,具體見第36和37頁),以及我們隨後的SEC申報文件,您可以在sec.gov查閱。
Contact:
聯繫方式:
Meera Lakhani-Patel
Veeva Systems
+44-790-430-0698
[email protected]
梅拉·拉可哈尼-帕特爾
veeva systems
+44-790-430-0698
[email protected]
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