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Scientific Communications Development

Medical Writing

Payer Advisory Board Strategy

Market Access Advisory Panels

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KOL Relationship Management

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Stakeholder Influence Mapping

Defining the Value of Medical Affairs

Evidence Generation

103

Clinical Trial Concepts

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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

103

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

187

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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Multi-Channel Campaign Launch

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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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Deviation Investigation

Corrective Action Verification

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Labeling & Packaging

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Evidence Prioritization

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Study Operations & Management

133

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Show More (1)

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Show Less (1)

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Clinical Study Report Writing

Abstract & Poster Development

Manuscript Development

Product Development

261

Clinical Research Network Development

Analytical Methods Development

Clinical Research

156

Clinical Trial Material Supply

Clinical Trials

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

Supply Chain Automation

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150

Data Curation

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Early Development

Clinical Trial Management Systems

Clinical Supply Chain Automation

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101

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A Trusted CRO Partner for End-to-End Drug Development

Biomapas provides comprehensive clinical research, regulatory affairs, pharmacovigilance, and medical information services for the biopharmaceutical and medical device industries across Europe, CIS, EAEU, MENA, LATAM, and the US. With expertise spanning the entire product lifecycle, Biomapas acts as an extension of your team to accelerate development, achieve authorization, and ensure compliance.

Whether you need to set up a pharmacovigilance system, conduct multinational clinical trials, or manage post-authorization requirements, Biomapas has the reach and capabilities to seamlessly support your global programs. Their tailored solutions and hands-on approach enable efficient, cost-effective execution that meets milestones and exceeds expectations.

A Trusted CRO Partner for End-to-End Drug Development

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