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Welcome to Ennov Insider
Take advantage of the knowledge and best practices gained from more than 20 years of research, innovation and development for the health and life sciences sectors.
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Compliance Without Compromise: Med Device Edition
Medical device companies must navigate the complexities of new regulations like the EU’s MDR/IVDR and the FDA’s UDI requirements. These mandates demand a higher
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IDMP without Data Re-entry
Join us on a journey to discover the key strategies for streamlining IDMP compliance without the burden of data re-entry.
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Navigate PV Safety with Confidence, Gain Instant Insights, and Take Action!
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Ennov’s Agnostic Solution for IDMP, the EASI connector
How are you going to be ready for IDMP compliance? Ennov has the answer.
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PV Made Simple
Are you looking for a transformative solution to streamline your PV processes without compromising compliance?
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Streamlining your eTMF: 10 Best Practices for Reducing Both Effort and Risk
Are you looking to maximize the efficiency of your electronic Trial Master File (eTMF) while minimizing effort and risk? Look
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Why SMBs should choose a right-sized RIM
Maximize your regulatory team’s potential with a right-sized RIM. Learn how SMBs can bring products to market faster with fewer resources.
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Sponsor Oversight and the Role of eTMF
Sponsor oversight of TMFs is a critical regulatory requirement for clinical trials, but it can be challenging to know where
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Benefits of Implementing an End-to-end RIM Platform
Why should you consider a Regulatory Platform instead of a standalone RIM solution? In less than 30 minutes, learn first steps, realistic objectives, and business benefits.
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Leveraging RIM for DADI and IDMP | Ep 3: Examples of Divergence
Explore concretes examples of divergence between a RIM data model and HA guidance data format.
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Leveraging RIM for DADI and IDMP | Ep 2: Enterprise-Level Data Architecture
Learn about enterprise-level data architecture using master level data management.
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Leveraging RIM for DADI and IDMP | Ep 1: Best Practices for Data Modeling
Discover the best practices for RIM Data modeling in the context of IDMP.
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eTMF for Risk Management and Regulatory Compliance | Ep. 6: Sponsor Access
Episode 6 of our mini-series explores TMF Sponsor Access for Risk Management & Regulatory Compliance.
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eTMF for Risk Management and Regulatory Compliance | Ep. 5: TMF Inspections
Episode 5 of our mini-series explores TMF Inspections for Risk Management & Regulatory Compliance.
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eTMF for Risk Management and Regulatory Compliance | Ep. 4: TMF Quality
Episode 4 of our mini-series explores TMF Quality for Risk Management & Regulatory Compliance.
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eTMF for Risk Management and Regulatory Compliance | Ep. 3: TMF Timeliness
Episode 3 of our mini-series explores TMF Timeliness for Risk Management & Regulatory Compliance.
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eTMF for Risk Management and Regulatory Compliance | Ep. 2: TMF Completeness
Episode 2 of our mini-series explores TMF Completeness for Risk Management & Regulatory Compliance.
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eTMF for Risk Management and Regulatory Compliance | Ep. 1: Guidance Review
Episode 1 of our mini-series explores TMF Guide Review for Risk Management & Regulatory Compliance.
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Visualize Your Clinical Risk and Status with Ennov Analytics
This webinar showcases one of our newest products – Ennov Analytics, our powerful yet easy-to-use reporting and data visualization software. This presentation focuses on its use in conjunction with Ennov CTMS, our highly capable Clinical Trial Management solution.
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Visualize Your Regulatory Risk and Status with Ennov Analytics
Learn how Ennov Analytics frees you from data gathering and spreadsheet manipulation by providing targeted dashboards where you can complete a precise analysis with just a few clicks.
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Accelerate Time to Value by Leveraging Predefined Regulatory Processes
Learn how to decrease the time required to implement Regulatory Information Management systems using a streamlined approach.
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Pharmacovigilance Signal Detection and Data Analysis
Learn how PV-Analyzer can help prepare statistical detailed analyses of safety data to reduce risk
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Migrating Legacy Documents to Ennov
Learn best practices for migrating documents from legacy systems into Ennov.
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Ennov and 21 CFR Part 11
Learn how Ennov enables compliance with the US FDA’s 21 CFR Part 11 guidance.