InstantGMP推出软件成功的五点实施计划-动脉网

InstantGMP Launches 5-Point Implementation Plan for Software Success

CISION 等信源发布 2025-04-16 21:28

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CARY, N.C.

北卡罗来纳州凯里市

，

April 16, 2025

2025年4月16日

/PRNewswire/ --

InstantGMP™

即时GMP™

, a leading provider of GMP-compliant software solutions for pharmaceutical and regulated manufacturing, is proud to announce the launch of its 5-Point Implementation Plan, a strategic, streamlined onboarding process designed to help new clients achieve

，一家为制药和受监管制造业提供符合GMP规范的软件解决方案的领先供应商，自豪地宣布推出其五点实施计划，这是一项战略性、简化的入职流程，旨在帮助新客户实现目标。

GMP success

GMP 成功

faster and more effectively.

更快更有效地。

The new

新的

5-Point Implementation Plan

五点实施计划

is based on years of hands-on experience and

基于多年实际操作经验，并且

direct feedback from clients

客户直接反馈

across the pharmaceutical, biotech, dietary supplement, and cannabis industries. This structured approach to manufacturing software implementation provides a clear roadmap that ensures each customer, regardless of their starting point, receives the support, guidance, and tools needed to unlock the full potential of the .

跨制药、生物技术、膳食补充剂和大麻行业。这种结构化的制造软件实施方法提供了一个清晰的路线图，确保每个客户，无论他们的起点如何，都能获得支持、指导和工具，以充分释放潜力。

InstantGMP™ PRO

InstantGMP™ 专业版

pharmaceutical manufacturing software.

制药生产软件。

'The best software won't deliver results without the right implementation behind it,' said Dr.

“最好的软件如果没有正确的实施，也无法产生结果，”博士说道。

Richard Soltero

理查德·索尔特罗

, President of InstantGMP

，InstantGMP总裁

. 'We designed our implementation plan to be collaborative, customizable, and comprehensive so that our customers feel confident and in control from day one.'

“我们设计的实施计划旨在实现协作、可定制和全面，让客户从第一天起就感到信心十足并掌控全局。”

The 5 Phases of the Implementation Plan include:

实施计划的五个阶段包括：

Phase 1: Planning & System Design:

第一阶段：规划与系统设计：

A virtual kick-off meeting to define scope, goals, responsibilities, and project timelines.

一个虚拟的启动会议，用于定义范围、目标、职责和项目时间表。

Phase 2: System Configuration & Implementation

第二阶段：系统配置与实施

: On-site configuration of

：现场配置

inventory

库存

，

equipment

设备

，

documents

文档

, and

，以及

LMS curricula

LMS 课程大纲

, including MPR entry and testing.

，包括MPR条目和测试。

Phase 3: Pilot Testing, Operator Training & Launch:

第三阶段：试点测试、操作员培训和启动：

On-site pilot project selection, training for operational and

现场试点项目的选择、操作培训和

quality roles

质量角色

, and live rollout with performance monitoring.

，并通过性能监控进行实时部署。

Phase 4: Optimization:

第四阶段：优化：

Virtual meetings to optimize workflows, refresh training, and fine-tune system functionalities.

虚拟会议以优化工作流程、更新培训并微调系统功能。

Phase 5: Ongoing Configuration Assistance:

第五阶段：持续的配置协助：

Continued support, virtually or on-site, including assistance with

持续支持，无论是虚拟的还是现场的，包括协助

dynamic fields

动态字段

，

scale integrations

规模集成

, or operational resets.

，或操作重置。

By combining expert-led training, live collaboration, and on-demand assistance, this implementation plan transforms software adoption into a structured, manageable, and measurable process that helps manufacturers meet

通过结合专家指导的培训、实时协作和按需协助，该实施计划将软件采用转变为一个结构化、可管理和可衡量的过程，帮助制造商满足需求。

FDA and GMP compliance standards

FDA和GMP合规标准

while maximizing operational efficiency.

同时最大化运营效率。

To learn more about InstantGMP's 5-Point Implementation Plan and how it can benefit your manufacturing operations,

要了解更多关于InstantGMP的5点实施计划及其如何使您的制造业务受益，

contact our sales team today

联系我们的销售团队今天

。

About InstantGMP™, Inc.

关于InstantGMP™公司

Founded by pharmaceutical industry veteran Dr.

由制药行业资深人士Dr.创立

Richard Soltero

理查德·索尔特罗

，

InstantGMP, Inc.

即时GMP公司

, offers affordable all-in-one manufacturing, inventory and quality software. The company develops cloud-based electronic batch record software and standard operating procedures specific to industries that are required to follow

，提供价格合理的全方位制造、库存和质量软件。该公司开发基于云的电子批记录软件和标准操作程序，专门针对需要遵循相关规定行业的具体情况。

FDA manufacturing regulations and Good Manufacturing Practices ('GMP')

FDA制造法规和良好生产规范（“GMP”）

。

As a manufacturing software company, InstantGMP™ pioneered accessible, easy-to-use

作为一家制造软件公司，InstantGMP™ 开创了易于访问、方便使用的软件

electronic batch record software

电子批记录软件

for products manufactured using GMPs. The Company's updated software simplifies the documentation and approval procedures for quality processes that keep all quality documentation organized in electronic format while providing for quality checks and workflow processes to make compliance with FDA requirements easy..

对于按照GMP生产的产品，公司更新的软件简化了质量流程的文档记录和审批程序，将所有质量文档以电子形式有序组织，同时提供质量检查和工作流程以轻松符合FDA要求。

SOURCE InstantGMP, Inc.

来源：InstantGMP, Inc.

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