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登録と申し込み

CARA forRIM™は、規制情報の強力なWebを提供し、データを管理して、組織全体での識別と再利用を容易にします。この一貫したグローバル情報はプロセスに出入りするため、効率が向上します。
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Generis Digital Transformation White Paper

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The Big Debate - The future will be data driven

Medical Writing

Area

Type

Clinical

Summary Page

CTMS

Area

Type

Clinical

Summary Page

eTMF

Area

Type

Clinical

White Paper

CARA Cloud Enterprise Platform

Area

Type

Cloud Adoption

Infographic

Optimising Digital Transformation in Regulated Industries

Area

Type

Digital Transformation

eBook

Structured Content Authoring

Area

Type

General

White Paper

The Big Debate

Area

Type

General

eBook

City of Sacramento Case Study

Area

Type

Government

Case Study

Pharmaceutical Labelling

Area

Type

Labelling

White Paper

'Where Used' Functionality on the CARA Life Sciences Platform

Area

Type

Life Sciences

Video

CARA for Life Sciences

Area

Type

Life Sciences

White Paper

Medical Device Process

Area

Type

Medical Devices

Diagram

Medical Devices

Area

Type

Medical Devices

White Paper

Inconsult Partner Spotlight

Area

Type

Partners

Partner Spotlight

Syneos Health Partner Spotlight

Area

Type

Partners

Partner Spotlight

DocShifter Partner Spotlight

Area

Type

Partners

Partner Spotlight

Daelight Partner Spotlight

Area

Type

Partners

Partner Spotlight

fme Partner Spotlight

Area

Type

Partners

Partnership

Batch Records Management

Area

Type

Quality

Data Sheet

Quality Management Infographic

Area

Type

Quality

Infographic

Quality Events Summary

Area

Type

Quality

Summary Page

Quality Docs and QMS

Area

Type

Quality

White Paper

The Big Debate : What Will Quality Management Look Like By 2025?

Area

Type

Quality

eBook

Building the business case for better Regulatory Information Management : 3 Key Considerations

Area

Type

RIM

ebook

Biogen Case Study

Area

Type

Regulatory

Case Study

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