Series topic: Vigilance Medical Device Guidance Part 1- topic: “Vigilance Medical Device Regulations (EU) 2017/745
Posted by Florence D. from Qinecsa Solutions18 days ago
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Clinical Research *
5
Clinical Reporting
3
Abstract & Poster Development
Clinical Study Report Writing
Manuscript Development
Product Development
8
Analytical Methods Development
Clinical Research
Clinical Trial Material Supply
Clinical Trials
Document Management
Show More (3)
Drug Product Manufacturing
Formulation Development
Submissions Management
Show Less (3)
Real World Data Research
5
Analytics Methods Development
Data Standardization & Curation
Late Phase Data Curation
Lifecycle Evidence Generation
Observational Research
Study Operations & Management
5
Patient Recruitment
Site Contracting & Payments
Site Identification & Activation
Site Relationship Management
Study Tracking & Analytics
Trial Design & Planning
5
Data Management Planning
Enrollment Analytics
Patient Recruitment Planning
Protocol Feasibility Planning
Statistical Analysis Planning
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2
Brand Planning & Activation
3
Brand Vision & Positioning
Campaign Concept Testing
Multi-Channel Campaign Launch
Customer Engagement
5
Omnichannel Optimization
Patient Engagement
Patient Facing Solution Design
Patient Journey Analysis
Retention Program Effectiveness
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2
Financial Services
4
Billing & Reporting Operations
Internal Audit Support
Investment Performance Analytics
Revenue Forecasting & Planning
Investment Banking
3
Buy & Sell Side Advisory
Capital Raising & Financing
Investor Relations
Market Access & Policy *
2
Global Market Access
3
Payer Evidence Generation
Payer Relationship Management
Reimbursement Consulting
Government Policy
2
Advocacy Management
Legislative Monitoring
Medical Affairs *
4
Evidence Generation
5
Clinical Trial Concepts
Health Economics Modeling
Internal Medical Education
Patient Journey Mapping
Research Gap Analysis
Scientific Communications Development
2
Market Access Advisory Panels
Payer Advisory Board Strategy
Strategic Communications Planning
3
Competitive Publications Analysis
Publication Planning
Scientific Platform Planning
Strategic Stakeholder Engagement
3
Advisory Board Strategy
KOL Relationship Management
Stakeholder Influence Mapping
Pharmacovigilance *
2
Risk Management
3
Risk Evaluation & Minimization
Risk Management Evaluation
Safety Communications
Safety Systems
3
Safety Data Analytics
Safety Data Intake & Triage
Safety Signal Evaluation
Quality & Mfg *
4
Facilities & Equipment
5
Calibration & PM Programs
Deviation Investigations
Equipment Maintenance
Facility Maintenance Programs
Facility Security Management
Production & Supply Chain
3
Clinical & Commercial Production
Labeling & Packaging
Storage & Distribution
Quality Management
3
Corrective Action Verification
Deviation Investigation
Quality Process Governance
Testing & Release
3
Batch Release Testing
Raw Material Testing
Stability Program Testing
Regulatory *
4
Compliance
5
Agency Meeting Support
Dossier & Application Development
eCTD Publishing & Validation
Pre-Submission Advisory Meetings
Regulatory Compliance
Labeling & Promotions
2
Core Data Sheet Management
Labeling Strategy Development
Maintenance & Renewals
3
Post-Approval Safety Reporting
Promotional Material Compliance
Variations & Supplements
Transparency & Disclosure
2
Clinical Disclosure
Clinical Transparency
Technology & Operations *
6
Automation & Efficiency
3
Clinical Data Automation
Lab Automation Systems
Supply Chain Automation
Data & Analytics
3
Advanced Analytics
Data Curation
Data Visualization
Digital Health Solutions
6
5G Infrastructure
Blockchain Applications
mHealth Applications
Patient Portals
Telemedicine Platforms
Show More (1)
Wearables & Sensors
Show Less (1)
Early Development
2
Clinical Supply Chain Automation
Clinical Trial Management Systems
Informatics Infrastructure
3
Cloud Computing Systems
Data Security Solutions
Data Storage Platforms
Operations
11
Communications
Communications & Corporate Affairs
Content Creation & Development
Human Resources & Talent Acquisition
Management Consulting
Show More (6)
Marketing
Medical Information Services
Medical Writing
Operations Management
Other
Public Relations
Show Less (6)
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Back
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!
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