Empowering pharmaceutical companies with trusted, standardized product data

为制药公司提供可信、标准化的产品数据支持

AACHEN, Germany, October 20, 2025 / Biotech Newswire / --

德国亚琛，2025年10月20日 /生物技术新闻社/ --

ACCURIDS

准确识别系统

, the IDMP Data Standardization Fabric for Life Sciences, today announced it has joined the

，生命科学领域的IDMP数据标准化平台，今天宣布其已加入

Veeva Product Partner Program

Veeva产品合作伙伴计划

. This collaboration enables pharmaceutical companies to integrate ACCURIDS with

。此次合作使制药公司能够将ACCURIDS与

Veeva Vault applications

Veeva Vault 应用程序

– including Regulatory, Clinical, Safety, and Quality – to accelerate compliance and improve data quality across departments.

——包括法规、临床、安全和质量——以加速合规并提高各部门的数据质量。

ACCURIDS provides regulatory and product data with

ACCURIDS 提供法规和产品数据 với

identity, context, and clarity

身份、背景和清晰度

, ensuring that information can be trusted, shared, and reused throughout the medicinal product lifecycle. Purpose-built for the pharmaceutical industry, the platform helps organizations overcome key data challenges such as

，确保信息在整个药品生命周期中可以被信任、共享和重复使用。该平台专为制药行业量身打造，帮助组织克服关键的数据挑战，例如

IDMP alignment, regulatory compliance, data quality management

IDMP 对齐、法规遵从、数据质量管理

, and

，以及

submission readiness

提交准备情况

.

。

With the

随着

Veeva RIM connector

Veeva RIM 连接器

and the

和

EMA PMS API

EMA PMS API

, ACCURIDS is now the

，ACCURIDS现在是

first out-of-the-box software solution

首个开箱即用的软件解决方案

enabling

启用

end-to-end data comparison for proactive monitoring of product compliance

端到端数据对比，用于产品合规性的主动监控

. This innovation allows regulatory and product teams to identify discrepancies early, ensure continuous data alignment, and maintain compliance throughout the product lifecycle.

这一创新使监管团队和产品团队能够及早发现差异，确保数据的持续一致，并在整个产品生命周期中保持合规性。

Through the integration with Veeva Vault, life sciences companies benefit from:

通过与Veeva Vault的集成，生命科学公司受益于：

• Higher automation in regulatory data standardization and submission processes

• 监管数据标准化和提交流程的更高自动化

• Improved efficiency in maintaining high-quality, compliant product data

• 提高了维护高质量、合规产品数据的效率

• Reduced manual effort and faster onboarding through semantic harmonization

通过语义协调减少人工投入并加快入职速度

• Consistent, reusable data across regulatory and other critical business functions

• 在监管和其他关键业务功能中保持一致、可重复使用的数据

“Joining the Veeva Product Partner Program is a major milestone for us and our customers,” said

“加入Veeva产品合作伙伴计划对我们及我们的客户来说都是一个重要的里程碑，”表示

Heiner Oberkampf, CEO of ACCURIDS

海纳·奥伯坎普夫，ACCURIDS首席执行官

. “By connecting our data standardization platform with Veeva Vault, we enable pharmaceutical companies to automate data flows, ensure consistency and quality, and unlock value across the entire product lifecycle.”

“通过将我们的数据标准化平台与Veeva Vault连接，我们使制药公司能够自动化数据流，确保一致性和质量，并在整个产品生命周期中释放价值。”

This partnership underscores ACCURIDS’ commitment to

这一合作关系强调了ACCURIDS的承诺

precision, innovation, and scalability

精度、创新和可扩展性

– empowering pharmaceutical companies to fully leverage their regulatory and product data without the complexity of custom integrations.

- 赋能制药公司充分利用其监管和产品数据，而无需面对定制集成的复杂性。

About

关于

ACCURIDS

准确识别

ACCURIDS is the

ACCURIDS 是

IDMP Data Standardization Fabric

IDMP数据标准化架构

for the pharmaceutical industry. The platform gives product data

对于制药行业。该平台提供产品数据

identity, context, and clarity

身份、背景和清晰度

– enabling organizations to harmonize, validate, and reuse regulatory and product data while ensuring compliance with global standards and delivering value across the entire medicinal product lifecycle.

- 使组织能够协调、验证和重复使用监管和产品数据，同时确保符合全球标准，并在整个医药产品生命周期中提供价值。

Contact

联系

ACCURIDS

准确识别

Walid Atai

瓦利德·阿泰

Business Development,

商务拓展，

This email address is being protected from spambots. You need JavaScript enabled to view it.

该电子邮件地址正受到防垃圾邮件机器人的保护。您需要启用 JavaScript 才能查看它。

Keywords: Data Accuracy; Reference Standards; Automation; Software; Germany; ACCURIDS; Veeva Product Partner Program; pharmaceutical companies; product data standardization; trusted data; IDMP Data Standardization Fabric; life sciences; Veeva Vault integration; regulatory compliance; data quality; data management; medicinal product lifecycle; IDMP alignment; submission readiness; Veeva RIM connector; EMA PMS API; end-to-end data comparison; product compliance monitoring; regulatory data standardization; automation; semantic harmonization; data consistency; data reuse; onboarding acceleration; Heiner Oberkampf; data standardization platform; data harmonization; data validation; regulatory data quality; product data lifecycle; global standards compliance.

关键词：数据准确性；参考标准；自动化；软件；德国；ACCURIDS；Veeva产品合作伙伴计划；制药公司；产品数据标准化；可信数据；IDMP数据标准化架构；生命科学；Veeva Vault集成；法规合规性；数据质量；数据管理；医药产品生命周期；IDMP对齐；提交准备；Veeva RIM连接器；EMA PMS API；端到端数据对比；产品合规性监控；法规数据标准化；自动化；语义协调；数据一致性；数据重用；上手加速；Heiner Oberkampf；数据标准化平台；数据协调；数据验证；法规数据质量；产品数据生命周期；全球标准合规性。

Source: Biotech Newswire

来源：生物技术新闻专线