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.
Artwork Management Made Easy (w. practical examples)
Optimizing Artwork Management in Regulatory Processes Join us for a 30-minute webinar on improving Artwork management through standardized, compliant
How to Save Time Managing Agency Correspondence with AI
The increased volume of health authority interactions in the review and approval cycle has created a commensurate challenge for life
Effective Training Management Powered by AI
Proving training records to regulatory authorities? Our AI-powered solution automatically generates compliance assessments from your documentation—no more manual effort, just
Effortless Data Enrichment for IDMP Compliance
Meeting the EMA’s IDMP requirements is critical, but it doesn’t have to be complicated. Ennov’s powerful automated solution simplifies PMS
Aligning RIM and PMS: Challenges for a Systematic Comparison
Discover essential strategies in this informative session with Ennov’s own Pierre Stanislawski and Maxime Delpire, as they dive into the
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
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.
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.
PV Made Simple
Are you looking for a transformative solution to streamline your PV processes without compromising compliance?
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
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.
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
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.
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.
Leveraging RIM for DADI and IDMP | Ep 2: Enterprise-Level Data Architecture
Learn about enterprise-level data architecture using master level data management.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Pharmacovigilance Signal Detection and Data Analysis
Learn how PV-Analyzer can help prepare statistical detailed analyses of safety data to reduce risk
Migrating Legacy Documents to Ennov
Learn best practices for migrating documents from legacy systems into Ennov.
Ennov and 21 CFR Part 11
Learn how Ennov enables compliance with the US FDA’s 21 CFR Part 11 guidance.