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Medical Affairs *

Scientific Communications Development

Medical Writing

Payer Advisory Board Strategy

Market Access Advisory Panels

Strategic Stakeholder Engagement

KOL Relationship Management

Advisory Board Strategy

Stakeholder Influence Mapping

Defining the Value of Medical Affairs

Evidence Generation

104

Clinical Trial Concepts

Internal Medical Education

Health Economics Modeling

Patient Journey Mapping

Research Gap Analysis

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Medical and Scientific Communications

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117

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Medical Affairs *

Scientific Communications Development

Medical Writing

Payer Advisory Board Strategy

Market Access Advisory Panels

Strategic Stakeholder Engagement

KOL Relationship Management

Advisory Board Strategy

Stakeholder Influence Mapping

Defining the Value of Medical Affairs

Evidence Generation

104

Clinical Trial Concepts

Internal Medical Education

Health Economics Modeling

Patient Journey Mapping

Research Gap Analysis

Strategic Communications Planning

Publication Planning

Medical and Scientific Communications

Scientific Platform Planning

Competitive Publications Analysis

Regulatory *

Labeling & Promotions

Labeling Strategy Development

Core Data Sheet Management

Maintenance & Renewals

Variations & Supplements

Post-Approval Safety Reporting

Promotional Material Compliance

Compliance

186

Regulatory Compliance

117

Dossier & Application Development

Pre-Submission Advisory Meetings

eCTD Publishing & Validation

Agency Meeting Support

Show More (1)

Structured Content Authoring

Show Less (1)

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Clinical Disclosure

Clinical Transparency

Commercialization *

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Patient Engagement

Patient Facing Solution Design

Patient Journey Analysis

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Show More (1)

Retention Program Effectiveness

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Multi-Channel Campaign Launch

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Government Policy

Legislative Monitoring

Advocacy Management

Global Market Access

Payer Evidence Generation

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Reimbursement Consulting

Payer Relationship Management

Launch Sequencing

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Safety Systems

Safety Database Hosting

Signal Detection

Case Processing

Safety Data Intake & Triage

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Literature Searching

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Facility Maintenance Programs

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Deviation Investigation

Corrective Action Verification

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Production & Supply Chain

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Labeling & Packaging

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Study Operations & Management

133

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Clinical Study Report Writing

Abstract & Poster Development

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262

Clinical Research Network Development

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Clinical Research

156

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110

Show More (4)

Drug Product Manufacturing

Submissions Management

Formulation Development

Document Management

Show Less (4)

Trial Design & Planning

Protocol Feasibility Planning

Statistical Analysis Planning

Enrollment Analytics

Patient Recruitment Planning

Data Management Planning

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Lab Automation Systems

Clinical Data Automation

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149

Data Curation

Artificial Intelligence

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Early Development

Clinical Trial Management Systems

Clinical Supply Chain Automation

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101

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5 Independence Way Ste 300, Princeton, NJ 08540, USA

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Trusted Document Management for Life Sciences

DACHS

has been building its full-service IT business for over 20 years based on excellent human minds committed to delivering great solutions to the Life Sciences and healthcare industry. Our primary focus is to develop and support document management systems that enable the release of new medications and treatments strictly complying with governing regulations to ultimately reach those who need them. With over 20 years of experience and 250+ projects completed, DACHS offers reliable and competent IT services including content management, data migration, software development, and technical support to boost effectiveness in controlled environments.

Trusted Document Management for Life Sciences

DACHS

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5 Independence Way Ste 300, Princeton, NJ 08540, USA

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