Series topic: Vigilance Medical Device Guidance Part 1- topic: “Vigilance Medical Device Regulations (EU) 2017/745
Posted by Kalina S.Qinecsa Solutions
239 days ago
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Clinical Research *
Clinical Reporting
9
Abstract & Poster Development
3
Clinical Study Report Writing
7
Manuscript Development
1
Product Development
204
Analytical Methods Development
1
Clinical Research
120
Clinical Research Network Development
1
Clinical Trial Material Supply
3
Clinical Trials
74
Show More (4)
Document Management
5
Drug Product Manufacturing
3
Formulation Development
1
Submissions Management
2
Show Less (4)
Real World Data Research
28
Analytics Methods Development
3
Data Standardization & Curation
3
Evidence Prioritization
1
Late Phase Data Curation
7
Lifecycle Evidence Generation
2
Show More (1)
Observational Research
14
Show Less (1)
Study Operations & Management
113
Patient Recruitment
20
Site Contracting & Payments
2
Site Identification & Activation
11
Site Relationship Management
2
Study Tracking & Analytics
79
Show More (1)
Trial Implementation
1
Show Less (1)
Trial Design & Planning
65
Data Management Planning
7
Enrollment Analytics
3
Patient Recruitment Planning
43
Protocol Feasibility Planning
7
Software
1
Show More (1)
Statistical Analysis Planning
6
Show Less (1)
Commercialization *
Brand Planning & Activation
15
Brand Vision & Positioning
7
Campaign Concept Testing
1
Multi-Channel Campaign Launch
7
Customer Engagement
46
Omnichannel Optimization
12
Patient Engagement
2
Patient Facing Solution Design
16
Patient Journey Analysis
7
Retention Program Effectiveness
11
Show More (1)
Strategic Account Management
1
Show Less (1)
Finance & Investment *
Financial Services
8
Billing & Reporting Operations
3
Internal Audit Support
1
Investment Performance Analytics
3
Revenue Forecasting & Planning
1
Investment Banking
6
Buy & Sell Side Advisory
3
Capital Raising & Financing
4
Investor Relations
0
Market Access & Policy *
Global Market Access
57
Launch Sequencing
1
Payer Evidence Generation
3
Payer Relationship Management
16
Pricing Strategy
2
Reimbursement Consulting
41
Government Policy
2
Advocacy Management
1
Legislative Monitoring
2
Medical Affairs *
Defining the Value of Medical Affairs
1
Defining the Value of Medical Affairs
1
Evidence Generation
101
Clinical Trial Concepts
15
Health Economics Modeling
60
Internal Medical Education
20
Patient Journey Mapping
3
Research Gap Analysis
5
Scientific Communications Development
10
Market Access Advisory Panels
2
Payer Advisory Board Strategy
9
Strategic Communications Planning
32
Competitive Publications Analysis
5
Publication Planning
4
Scientific Platform Planning
24
Strategic Stakeholder Engagement
68
Advisory Board Strategy
41
KOL Relationship Management
8
Stakeholder Influence Mapping
29
Pharmacovigilance *
Risk Management
22
Risk Evaluation & Minimization
19
Risk Management Evaluation
5
Safety Communications
3
Safety Systems
85
Safety Data Analytics
35
Safety Data Intake & Triage
33
Safety Signal Evaluation
25
Quality & Mfg *
Facilities & Equipment
13
Calibration & PM Programs
1
Deviation Investigations
0
Equipment Maintenance
0
Facility Maintenance Programs
8
Facility Security Management
4
Production & Supply Chain
54
Clinical & Commercial Production
28
Labeling & Packaging
17
Storage & Distribution
22
Quality Management
82
Corrective Action Verification
51
Deviation Investigation
8
Quality Process Governance
25
Testing & Release
16
Batch Release Testing
2
Raw Material Testing
12
Stability Program Testing
3
Regulatory *
Compliance
153
Agency Meeting Support
45
Dossier & Application Development
22
eCTD Publishing & Validation
10
Pre-Submission Advisory Meetings
2
Regulatory Compliance
89
Labeling & Promotions
2
Core Data Sheet Management
1
Labeling Strategy Development
1
Maintenance & Renewals
9
Post-Approval Safety Reporting
4
Promotional Material Compliance
4
Variations & Supplements
3
Transparency & Disclosure
4
Clinical Disclosure
2
Clinical Transparency
3
Technology & Operations *
Automation & Efficiency
8
Clinical Data Automation
6
Lab Automation Systems
1
Supply Chain Automation
1
Data & Analytics
80
Advanced Analytics
34
Artificial Intelligence
1
Data Curation
8
Data Visualization
44
Digital Health Solutions
75
5G Infrastructure
3
Blockchain Applications
0
mHealth Applications
5
Patient Portals
24
Telemedicine Platforms
22
Show More (1)
Wearables & Sensors
23
Show Less (1)
Early Development
3
Clinical Supply Chain Automation
1
Clinical Trial Management Systems
2
Informatics Infrastructure
74
Cloud Computing Systems
51
Data Security Solutions
17
Data Storage Platforms
8
Operations
61
Communications
1
Communications & Corporate Affairs
0
Content Creation & Development
6
Human Resources & Talent Acquisition
27
Management Consulting
2
Show More (7)
Marketing
24
Medical Information Services
0
Medical Writing
2
Operations Management
0
Other
4
Product/Service
0
Public Relations
1
Show Less (7)
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Back
Qinecsa Solutions
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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