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Home Suppliers Qinecsa Solutions Featured Content Series topic: Vigilance Medical Device Guidance Part 1- topic: “Vigilance Medical Device Regulations (EU) 2017/745

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Scientific Communications Development

Medical Writing

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Market Access Advisory Panels

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KOL Relationship Management

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Defining the Value of Medical Affairs

Evidence Generation

103

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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

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Structured Content Authoring

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Clinical Transparency

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Patient Engagement

Patient Facing Solution Design

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Retention Program Effectiveness

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Multi-Channel Campaign Launch

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Government Policy

Legislative Monitoring

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Global Market Access

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Reimbursement Consulting

Payer Relationship Management

Launch Sequencing

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Safety Database Hosting

Signal Detection

Case Processing

Safety Data Intake & Triage

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Safety Data Analytics

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Literature Searching

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Capital Raising & Financing

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Equipment Maintenance

Facility Maintenance Programs

Facility Security Management

Deviation Investigations

Calibration & PM Programs

Testing & Release

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Batch Release Testing

Raw Material Testing

Quality Management

Deviation Investigation

Corrective Action Verification

Quality Process Governance

Production & Supply Chain

Storage & Distribution

Labeling & Packaging

Clinical & Commercial Production

Clinical Research *

Real World Data Research

Data Standardization & Curation

Late Phase Data Curation

Analytics Methods Development

Lifecycle Evidence Generation

Real World Evidence

Show More (2)

Evidence Prioritization

Observational Research

Show Less (2)

Study Operations & Management

133

Site Contracting & Payments

Study Tracking & Analytics

Site Relationship Management

Trial Implementation

Site Identification & Activation

Show More (1)

Patient Recruitment

Show Less (1)

Clinical Reporting

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

Show More (1)

Software

Show Less (1)

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Automation & Efficiency

Lab Automation Systems

Clinical Data Automation

Supply Chain Automation

Data & Analytics

150

Data Curation

Artificial Intelligence

Data Visualization

Advanced Analytics

Early Development

Clinical Trial Management Systems

Clinical Supply Chain Automation

Digital Health Solutions

101

5G Infrastructure

mHealth Applications

Patient Portals

Blockchain Applications

Telemedicine Platforms

Show More (1)

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Medical Writing

Management Consulting

Other

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Series topic: Vigilance Medical Device Guidance Part 1- topic: “Vigilance Medical Device Regulations (EU) 2017/745

Posted by

Kalina

431 days ago

Join our insightful webinar exploring the latest developments in the EU medical device vigilance landscape, with industry-renowned specialist Veronika Valdova. Learn how to seamlessly integrate medical devices into your pharma portfolio, gain practical strategies for navigating regulations, and establish robust management processes.

Key topics include:
• Introduction to Medical Device Regulatory Requirements
• Addressing Practical Challenges
• Key Takeaways
• Q&A Session

🎯 This webinar is ideal for:
• MedTech company leaders in acquisition by pharma
• Pharma company leaders expanding their portfolio to include device products.

For any questions about this webinar, or if you would like to request the recording, please write to: contact@qinecsa.com. Enjoy!