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Qinecsa Solutions
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Clinical Research *
Clinical Reporting
Product Development
Real World Data Research
Study Operations & Management
Trial Design & Planning
Commercialization *
Brand Planning & Activation
Customer Engagement
Finance & Investment *
Financial Services
Investment Banking
Market Access & Policy *
Global Market Access
Government Policy
Medical Affairs *
Defining the Value of Medical Affairs
Evidence Generation
Scientific Communications Development
Strategic Communications Planning
Strategic Stakeholder Engagement
Pharmacovigilance *
Risk Management
Safety Systems
Quality & Mfg *
Facilities & Equipment
Production & Supply Chain
Quality Management
Testing & Release
Regulatory *
Compliance
Labeling & Promotions
Maintenance & Renewals
Transparency & Disclosure
Technology & Operations *
Automation & Efficiency
Data & Analytics
Digital Health Solutions
Early Development
Informatics Infrastructure
Operations
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Qinecsa Solutions
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Qinecsa Solutions is a reliable international collaborator uniting top-notch technology and scientific proficiency to link life science enterprises with optimal safety solutions.
Qinecsa Solutions is a reliable international collaborator uniting top-notch technology and scientific proficiency to link life science enterprises with optimal safety solutions.
Products (2/3)
Drug Safety Services
Complete pharmacovigilance and medical information services Supported by the highest caliber of medical and scientific staff to generate vital safety insights, rapidly.
Drug Safety Technology Products
Industry-leading technologies to support the pharmacovigilance landscape Supporting the needs of today with a clear roadmap to support the future requirements of the life sciences industry.
Featured Content (2)
by
Tina Fumic
🕒 Multiple time slots:
Americas: 6am | 10am | 2pm EDT
Europe: 12pm | 4pm | 8pm CET
⏳ Duration: 30 minutes
What To Expect:
Join us for a focused and dynamic 30-minute session where our expert speaker dives into the latest advancements in pharmacovigilance literature screening:
✓ Gain expert insights into literature screening processes
✓ Leverage AI and automation
✓ Discover practical solutions to industry pain points
✓ Learn about emerging trends shaping the future of pharmacovigilance
✓ Q&A to address your specific questions
About The Speaker:
✓ 20+ years in clinical practice & pharmacovigilance
✓ Experienced in literature screening solutions
✓ Skilled client partner
Register Now
Can't make it? Request the recording
Join us for Part 2 of our webinar series on post-marketing safety surveillance, where we dive deeper into the intricate world of medical devices and drug-device combination products.
Building upon the foundation set in Part 1, this session explores the reporting essentials and obligations associated with the post-marketing safety surveillance of these products in both the EU and USA markets. Industry expert Veronika Valdova will guide you through current trends and challenges in the industry, offering valuable insights into best practices and regulatory expectations. Attendees will gain a comprehensive understanding of how to navigate the complexities of safety surveillance and ensure compliance with international standards.
Agenda:
- Introduction Drug-Device and Combination Products.
- Types of DDCs in Europe and the U.S.
- Reporting Essentials and Obligations
- Essential Procedures to Cover
- Comparison of Reporting Requirements in the EU vs the U.S.
- Current Trends and/or Challenges
- Best Practices
- Key Takeaways
- Q & A Session
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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Qinecsa Solutions UK
Leman Street, London, ENG, GBR
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Insife
Revolutionizing Pharmacovigilance with Cutting-Edge Technology Insife is a leading provider of pharmacovigilance solutions, offering a comprehensi...
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