Simpler at every step.

Streamline your regulatory compliance systems and processes with our new end-to-end regulatory technologies, advisory and tech-enabled services. Free your team from labor-intensive tasks and maintenance to focus more on delivering valuable products to market.

让我们谈谈

>2,000 changes

自1998年以来的FDA法规中
"Disruptive Trends in Pharma Regulation", PwC, Pharmaboardroom.com, June 2018

53% of CEOs

在全球生命科学中,考虑行业法规是最大的破坏性业务趋势

Explore our comprehensive regulatory capabilities

Regulatory compliance has long been viewed as a cost center and a necessity, but leading organizations are recognizing opportunities for innovation in this space.

iqvia综合全球合规性Ronan Brown,高级副总裁兼负责人

通过IQVIA监管生产力工具,可以负担得起的改善发行和电子提交周期时间。

IQVIA的新监管生产力工具使创作和PDF发布迅速有效。并且我们的验证工具可确保您提交给监管机构的内容在派遣之前处于技术合规性。

  • More easily prepare, publish, and validate eCTD and Non-eCTD electronic submissions
  • 提高效率并降低相关的基础设施成本
  • 使用直观,设计良好的界面最大化吞吐量
先试后买
做出承诺之前的测试驱动器。在免费试验中访问IQVIA生产力工具。发现他们如何简化监管人员的日常活动,改善周期时间并最大程度地减少风险。
要求免费试用

借助全面的RIM系统,公司可以更深入地了解其监管计划。

高级董事米歇尔·吉岑(Michelle Gyzen)
集成的全球合规性

RIM Smart – an intelligent, integrated approach to regulatory management.

RIM Smart is the modern regulatory information management solution built to increase speed, collaboration, efficiency and visibility across your entire global portfolio, improving performance at a lower cost.

IQVIA RIM SMART在云中安全地交付,为整个监管过程提供了互连,全面和智能的管理。

了解更多

信息和实施的单一来源

粉红色盒子
粉红色盒子

In future, authors’ and publishers’ jobs will be transformed by artificial intelligence with algorithms custom-built to manage the routine work, freeing up professionals to focus on higher-value activities.

Devjani Ghosh Dasgupta,博士主任
Global Regulatory Affairs

Lower administrative burden across the product lifecycle with IQVIA’s Global Regulatory Affairs services

Our experienced GRA team helps biopharma and medtech companies handle regulatory workflows more flexibly, productively and efficiently. From strategic regulatory advice to regulatory maintenance and lifecycle support, we’ve got you covered. IQVIA’s expert resources, streamlined processes and leading technologies provide

  • 优化的时间用于关键决策点
  • Regulatory and operational risk mitigation
  • Streamlined regulatory pathways
  • 灵活的方法,以产生更有信息的证据
  • Improved transparency and proactive problem-solving

参与当地资源以应付可变需求

Dealing with workload peaks can be difficult—and expensive. Deploy trusted IQVIA resources to meet your needs around the world and allow your in-house professionals to focus on innovation and strategy. Scale quickly and reduce fixed costs by using our local, highly skilled, knowledgeable professionals to handle your work—on-demand.

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