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
将内容审批时间从四周以上缩短和自动申报是加快上市速度的关键机会
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.
西班牙巴塞罗那,2024年11月21日 /PRNewswire/ — Veeva Systems(纽约证券交易所代码:VEEV)今天公布了2024年Veeva MedTech商业基准调查的结果,显示近70%的医疗技术组织依赖手动流程和本土应用程序来管理商业内容和索赔。如果没有专门构建的内容管理系统,医疗技术商业团队将面临上市延迟和日益增长的合规风险。
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.
尽管将索赔、证据和宣传材料联系起来很重要,但只有15%的组织通过中央数据存储库简化了流程,在该存储库中,索赔与证实直接相关。数据显示,商业内容和索赔管理有很大的改进机会,可以提高知名度和速度。
The benchmark survey of over 130 commercial medtech leaders found that:
对130多家商业医疗技术领导者的基准调查发现:
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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.
- 内容个性化越来越受到关注。超过80%的人正在寻求量身定制和指定消息的策略。在严格的监管要求下,在没有合适的系统的情况下大规模实现合规的个性化仍然是一项挑战。
- 真正的全渠道的数字资产管理(DAM)尚未到位。近 40% 的组织报告说没有建立 dAM 系统,这限制了对个性化内容的管理。在拥有 DaM 的受访者中,只有 31% 的人表示可以在整个营销部门使用它。
- 审批时间延长会导致机会错失。在使用手动流程或本土解决方案的医疗技术公司中,有60%的批准时间超过四周。营销资产平均要经过三到五轮的审查,这可能会延迟活动的启动,从而影响产品知名度和销售势头。
- 人工智能和内容自动化继续影响医疗科技。45% 的医疗技术组织认为,人工智能可以贡献的最重要领域是内容创作。
"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."
Veeva MedTech商业内容战略高级董事杰夫·戈尔斯基表示:“随着对更多个性化宣传材料的需求增长,医疗科技公司在遵守监管标准和准确反映产品功效和安全性方面面临规模和合规性挑战。”“这份报告显示,几乎每个医疗技术组织都有机会改善内容和索赔管理流程,从而加快上市速度、合规性和效率。”
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 MedTech 商业基准调查研究了促销内容和索赔管理的当前流程、挑战和未来改进机会。
Additional Information
For more on Veeva Vault PromoMats for MedTech, visit: veeva.com/medtech/PromoMats
Connect with Veeva on LinkedIn:
附加信息
有关适用于医疗技术的 Veeva Vault PromoMats 的更多信息,请访问:veeva.com/Medtech/promoMats
在 LinkedIn 上与 Veeva 联系:
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.
关于 Veeva 系统公司
Veeva是生命科学行业云软件领域的全球领导者。Veeva致力于创新、产品卓越和客户成功,为1,000多家客户提供服务,包括全球最大的生物制药公司和新兴生物技术公司。作为一家公益公司,Veeva致力于平衡所有利益相关者的利益,包括客户、员工、股东及其所服务的行业。欲了解更多信息,请访问 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 前瞻性陈述
本新闻稿包含有关Veeva产品和服务以及使用我们的产品和服务的预期结果或收益的前瞻性陈述。这些陈述基于我们当前的预期。实际结果可能与本新闻稿中提供的结果存在重大差异,我们没有义务更新此类声明。有许多风险可能会对我们的业绩产生负面影响,包括我们在截至2024年7月31日的10-Q表中披露的风险和不确定性,您可以在此处找到(可能影响我们业务的风险摘要见第36和37页),以及我们随后在sec.gov上访问的美国证券交易委员会文件中披露的风险和不确定性。
Contact:
联系人:
Meera Lakhani-Patel
Veeva Systems
+44-790-430-0698
[email protected]
米拉·拉哈尼-帕特尔
Veeva 系统
+44-790-430-0698
[电子邮件保护]
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