Beyond Silos: Unifying Quality & Regulatory
Welcome back to the Ennovation Podcast, where we bring you the latest trends, insights, and expertise in life sciences and regulatory affairs. This time, I’m joined by Paul Palmer, pharmaceutical…
Case Study: Vetoquinol
Discover how Ennov’s unified ecosystem eliminated vendor sprawl, standardized processes, and enabled internal teams to own their expansion, all while maintaining zero disruption to business operations.
From Siloes to Synergy: Aligning Quality & Regulatory Ops
Learn how unified platforms eliminate traditional system boundaries to accelerate compliance, reduce costs, and create competitive advantage.
Why life science companies are ditching Point Solutions for Unified Platforms
Picture this: Your Quality team discovers a manufacturing deviation requiring immediate global notifications. But instead of a streamlined response, disconnected systems force manual work: exporting data from Quality, reformatting for…
EMA IDMP Roadmap: PMS Data Alignment (Session 2 of 2)
As the EMA continues to refine its IDMP implementation approach — including adjustments to PMS migration rules — organizations must shift from a one-time data alignment effort to an ongoing…
Best Practices for Implementing RIM and QMS Systems in 2025
Life sciences organizations face mounting pressure to accelerate regulatory processes while maintaining rigorous quality standards. Whether ensuring compliance, expanding globally, or managing complex product portfolios, success depends on implementing Regulatory…
Ennov IDMP EASI Connector for RIM Integration
Meeting the EMA’s IDMP requirements is critical, but it doesn’t have to be complicated. Ennov’s powerful automated solution simplifies PMS data enrichment, saving you time and ensuring accuracy. Why It…
AI and Its Impact on Life Sciences
Discover how Generative AI is revolutionizing drug development, healthcare, and regulatory compliance, shaping the future of the industry.
IDMP & xEVMPD Compliance: How to Manage Structured Data for EMA and Global Regulatory Success
1. Introduction: Why IDMP and xEVMPD Matter More Than Ever If you work in regulatory affairs or operations in life sciences, you’ve likely encountered the terms IDMP and xEVMPD more…
Ennov Successfully Completes eCTD 4.0 Submission with EMA – Giving Customers a Head Start
Ennov is proud to be one of only four technology vendors to have successfully submitted an eCTD 4.0 test sequence as part of the European Medicines Agency’s (EMA) ongoing pilot. …
EMA IDMP Roadmap: Updates, Requirements and Impact on Industry (Session 1 of 2)
By the end of 2024, EMA released updated IDMP guidance and the PMS implementation guide, following key milestones including the go-live of PMS. Closely connected to SPOR, XEVMPD, SIAMED, and…
YORIK DRAFT – EMA IDMP Roadmap: Updates, Requirements and Impact on Industry (Session 1 of 2)
By the end of 2024, EMA updated the IDMP guidance and the Product Management Service (PMS) implementation guide after the achievement of some milestones including PMS go live. The EMA…
EMA IDMP Roadmap: Updates, Requirements and Impact on Industry (Session 1 of 2)
By the end of 2024, EMA released updated IDMP guidance and the PMS implementation guide, following key milestones including the go-live of PMS. Closely connected to SPOR, XEVMPD, SIAMED, and…
Inside Sales Executive (On-Site, Hybrid, Remote)
As a key member of the Customer Support team, the mission of the Customer Support Engineer is to answer customer requests and issues regarding to the usage of Ennov Software, from a functional or technical perspective. When required, the Customer Support Engineer will work with or escalate within different departments at Ennov, such as Hosting, Integration, Professional Services or Developers.
Introducing Ennov 10.4: Working Smarter Across the Life Sciences Lifecycle
Ennov 10.4 is here, thanks to the valuable feedback from our customers. This release reflects our ongoing commitment to delivering software solutions that truly bring value. Every update in 10.4…
Publishing: Common Issues and How to Improve Timelines
Regulatory teams know the feeling: your documentation is complete, the submission plan is sent, and yet, you're still waiting days for your submission to be ready for review. With regulatory…
AI Reality Check & The IDMP Countdown
Welcome back to the Ennovation Podcast, where we bring you the latest trends, insights, and expertise in life sciences and regulatory affairs. This time, I’m joined by Pierre Stanislawski, our…
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 click and go! What’s In It for You? 📝…
Sales Executive – Regulatory IT Solutions (Life Sciences)
As a key member of the Customer Support team, the mission of the Customer Support Engineer is to answer customer requests and issues regarding to the usage of Ennov Software, from a functional or technical perspective. When required, the Customer Support Engineer will work with or escalate within different departments at Ennov, such as Hosting, Integration, Professional Services or Developers.
Sales Executive – Pharmacovigilance/Clinical Trial IT Solutions (Life Sciences)
As a key member of the Customer Support team, the mission of the Customer Support Engineer is to answer customer requests and issues regarding to the usage of Ennov Software, from a functional or technical perspective. When required, the Customer Support Engineer will work with or escalate within different departments at Ennov, such as Hosting, Integration, Professional Services or Developers.
Is Your Portfolio Ready for Data Enrichment?
The EMA has taken a huge step towards IDMP implementation with the go live of the Product Management Service (PMS) and integration of PMS data into the e-Application Form (eAF). …
AI Vendor Checklist
Generative AI and LLMs are rapidly becoming essential in life sciences. To maximize impact, companies must critically assess use cases and choose vendors whose tools integrate seamlessly with their teams.
IDMP Starter Pack
The EMA is moving to a phased implementation, requiring MAHs to iteratively enrich data in the Product Management Service. With each stage demanding more information, early preparation is key. Without it, manual processes may become unsustainable. All MAHs face upcoming deadlines—act now to ensure your data, tools, and teams are ready.
MHRA consider dramatic changes to the regulation of medical devices and in vitro diagnostics
The MHRA recently closed their consultation on routes to market for medical devices and in vitro diagnostic devices. The consultation, which closed on 5 January 2025, asked for input on…
Artwork Management Made Easy (with practical examples)
This 30-minute webinar covers improving Artwork management through standardized, compliant processes. Learn how to better organize and control your Artwork content while ensuring efficiency and compliance. In this session, we…
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 sciences companies: increased workload and accelerated timelines to respond to agency questions and queries. The physical capture of…
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 click and go! Here's what you'll learn: Auto-Generated Assessments: Seamlessly align…
eCTD 4.0 & Medical Devices: What’s Happening in 2025?
Welcome to the Ennovation Podcast, where we bring you the latest trends, insights and expertise in life sciences and regulatory affairs. For the first episode, we're joined by Diarmuid Waide,…
eCTD 4.0: Key Milestones
eCTD 4.0 is one of the main focal points of the regulatory world and there has been significant progress over the last year, with some major steps to come in…
eCTD 4.0 Pilot Readiness Checklist
eCTD 4.0 is one of the main focal points of the regulatory world, and participating in an eCTD 4.0 pilot is a great opportunity to get experience with the future of regulatory submissions. Make sure you’re prepared and get the most out of your pilot experience!
Ennov Training
Streamline Training with a Learning Management System. Simplify compliance monitoring, evaluate staff proficiency, automate onboarding.
Ennov to Sponsor the 2025 DIA RSIDM Forum
Ennov is thrilled to announce our Platinum Sponsorship of the 2025 DIA Regulatory Submissions, Information, and Document Management (RSIDM) Forum. This highly anticipated event will take place February 3-5, 2025,…
Introducing Ennov 10.3
We are thrilled to announce the release of Ennov 10.3, delivering even greater satisfaction to our platform's users. This latest version introduces two significant new features: Enhanced AI Capabilities Ennov…
Product Management Service (PMS)
The Product Management Service (PMS) is a core element of the European Medicines Agency's (EMA) IDMP implementation. PMS provides a centralized, standardized database for managing medicinal product information across the…
IDMP at the EMA: The European Shortage Monitoring Platform
More than four years after the initial publication of the EMA’s IDMP Implementation Guide in February 2020, the EMA have taken their biggest step towards IDMP implementation yet with the…
Global eCTD Regulatory Updates
The eCTD framework is evolving—and with it, new requirements, tools, and harmonization efforts impact regulatory submissions worldwide.
Ennov and CognifAI Partner for AI-Driven Pharmacovigilance
Ennov, a leading provider of unified compliance software solutions for the Life Sciences, is pleased to announce a strategic partnership with CognifAI, an innovative AI solutions company specializing in pharmacovigilance.…
Ennov to Sponsor the 2024 Global Pharmaceutical Regulatory Affairs Summit
Ennov is excited to announce its sponsorship of the 2024 Global Pharmaceutical Regulatory Affairs Summit (GPRAS), a hybrid event taking place from October 22-24, 2024, at the Sheraton Brussels Airport,…
Why The Future of Pharma Starts with IDMP
The pharmaceutical industry is no stranger to complex regulations and compliance requirements. Among them, the Identification of Medicinal Products (IDMP) standards set by the European Medicines Agency (EMA) stand out…
Ennov to Exhibit at ICTMC 2024
Ennov will exhibit at the 7th International Clinical Trials Methodology Conference (ICTMC) 2024, being held from September 30 to October 3 at the EICC in Edinburgh, UK. At ICTMC 2024,…
Preparing for eCTD 4.0 Pilots
At Ennov, we have always encouraged participation in Health Authority (HA) pilot schemes for new and emerging technologies. By having an open platform of communication and collaboration we ensure that…
Ennov to Exhibit at RAPS Convergence 2024
Ennov is excited to announce our participation at RAPS Convergence 2024, the largest and most well-recognized annual gathering of global regulatory affairs professionals. This year, the event will take place…
Brexit’s Ripple Effect: Veterinary Safety Reporting in the UK
Brexit has sent shockwaves through numerous industries, with one of its less publicized but significant impacts being on veterinary safety data reporting. The UK's departure from the European Union has…
Transforming Regulatory Affairs for a Biopharma Leader
One of the world's largest and most respected biopharma companies selected Ennov for its world-class Regulatory Information Management (RIM) system. This leader in animal health now has its entire product…
Cut the Complexity: From Cumbersome Legacy Systems to Next-Gen Solutions
Small and mid-sized life sciences companies face big hurdles. They must follow strict regulations, meet rigorous quality standards, and adapt to rapidly changing digital technologies - all with limited resources…
Ennov Completes the Enterprise Technology Integration from Calyx
Ennov is proud to announce the successful integration of the Enterprise Technology division from Calyx into our organization. This strategic acquisition, completed on June 1, 2024, significantly enhances Ennov’s portfolio…
Ennov Artwork
Ennov Artwork offers a powerful set of tools focused on content management, allowing content to be itemized, annotated, proofed, and compared down to the pixel. Changes between versions can be…
Ennov RIM for Med Device
A tailored, agile, and comprehensive regulatory information management solution designed specifically for medical devices, enabling seamless global compliance, enhancing operational agility, and reducing the risk of non-compliance in the fast-evolving…
Future-Proofing Quality Management: A Guide for SMBs in Life Sciences
For small and mid-sized life sciences companies, maintaining quality standards amid constant industry evolution is an uphill battle. With limited resources and leaner teams, these businesses grapple with unique obstacles…
Gartner Insights: Maximize Your QMS Success with Peer Guidance
Implementing a Quality Management System (QMS) software is a pivotal step for any organization aiming to enhance their quality policies and standard operating procedures. Gartner’s recent report, “Peer Lessons Learned…
Ennov to Exhibit at the 2024 DIA Global Annual Meeting, June 16-20 in San Diego, CA
Ennov is set to exhibit at the 2024 DIA Global Annual Meeting, taking place from June 16-20 in San Diego, CA. Be sure to visit us at booth #1427! The…
How to Future-Proof MedDevice/MedTech Compliance
The medical device industry is at a pivotal point, grappling with significant regulatory updates like the European Union’s Medical Device Regulation (MDR) or the FDA’s Quality Management System Regulation (QMSR)…
Ennov to Sponsor the 2024 CDISC + TMF Europe Interchange
Ennov is pleased to announce that we will be attending the 2024 CDISC + TMF Europe Interchange. The event is set to take place in Berlin from April 24-26, and…
Ennov to Sponsor the Pronovea Pharma Summit 2024
Ennov is excited to announce our participation as a Bronze Sponsor in the upcoming Pronovea Pharma Summit 2024: Drug Safety and Risk Management. The summit is scheduled for April 24-25…
Accelerating Drug Development: Unpacking FDA’s Master Protocol Guidance
In December, FDA issued a draft guidance, Master Protocols for Drug and Biological Product Development. This guidance is currently in the public comment period; comments received to date can be…
New MoCRA Adverse Event Reporting Requirements: Impact on the Cosmetic Industry
Product safety and consumer protection stand at the forefront of the cosmetics industry, underpinned by regulatory frameworks like the Modernization of Cosmetics Regulation Act of 2022 and its 2023 amendment.…
Artificial Intelligence (AI)
A branch of computer science dedicated to creating systems capable of performing tasks that typically require human intelligence. These tasks include learning, decision-making, problem-solving, and pattern recognition.
Why Unified Platforms are the Future of Cosmetovigilance
In an industry where innovation meets stringent safety requirements, cosmetovigilance (CV) stands as the critical backbone of consumer protection and brand integrity. The enactment of the EU Cosmetics Regulation 1223/2009 has brought…
AI-Driven Cosmetovigilance Solution for the Global Leader in Luxury
In a pioneering collaboration, the leading entity in the luxury cosmetics industry, known for its commitment to innovation and quality since 1987, has partnered with Ennov to enhance consumer safety…
Dermatological Safety Assurance with Unified Platforms
The Challenge In the pursuit of dermatological excellence, maintaining the integrity of safety data is not merely an option; it is the bedrock of consumer trust. Companies bear the critical…
Ennov Announces Strategic Acquisition of Calyx’s ‘Enterprise Technology’ Division
In a landmark move for the life sciences industry, Ennov has acquired the 'Enterprise Technology' division from Calyx. This acquisition significantly expands Ennov's portfolio by integrating the advanced eClinical and…
Ennov Boosts Portfolio with Acquisition of DocShifter: The Market-Leading Document Transformation Solution
In a move that signifies a major advancement in the life sciences industry, Ennov, a leader in regulated content management solutions, has acquired DocShifter, a top provider of document automation…
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The New Wave of QMS [8/8]: Reflections & Looking Ahead
The horizon for Quality Management Systems (QMS) is brimming with opportunities, ready to revolutionize the Life Sciences field. As we conclude our blog series on the future of QMS, let's…
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The New Wave of QMS [7/8]: Cybersecurity Measures
In today's digitally-driven era, data plays a paramount role in shaping the trajectory of the Life Sciences industry. As organizations increasingly rely on digital tools and platforms for quality management,…
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The New Wave of QMS [6/8]: Flexibility & Adaptability
The Life Sciences sector, by its very nature, is in a state of continual evolution. Innovations in research, shifts in market dynamics, and alterations in regulatory landscapes mean that static…
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The New Wave of QMS [5/8]: User-Centric Interface
The global nature of the Life Sciences industry brings with it an inherent diversity—geographically spread teams, a variety of roles, and a broad range of technical expertise levels. Amidst this…
The Trust Equation: Safety, Branding, and Consumer Loyalty
In ethical skincare, the challenge is balancing safety, brand values, and consumer loyalty. Companies must align products with values, meet global safety standards, and navigate complexity during innovation and expansion.…
Ennov to Sponsor the 2024 DIA RSIDM Forum
Ennov is pleased to announce that we will be attending the 2024 DIA Regulatory Submissions, Information and Document Management (RSIDM) Forum as a Platinum Sponsor. This event will be held at the…
Holistic Beauty and Safety Compliance: Bridging the Gap
In holistic skincare, marrying natural wellness with global safety standards is challenging. Companies must ensure products are effective and safe while complying with diverse regulations in expanding markets. This balance…
Sustainability in Safety: The Cosmetovigilance Approach
In the organic skincare sector, balancing safety and sustainability is a challenge. Companies must meet strict safety standards while innovating eco-friendly products and navigating global regulations. Managing safety data sustainably,…
Streamlining Operations with Digital Cosmetovigilance
In dermatology and aesthetic medicine, operational efficiency is vital. Companies must manage safety data efficiently, uphold product safety, and streamline operations to innovate faster while meeting global safety regulations. Scaling…
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The New Wave of QMS [4/8]: Data-Driven Decisions
In today's digitized world, data is often termed as the "new oil." The Life Sciences industry, rich in complex processes and critical operations, generates vast amounts of data. But what's…
Case Study: Pharmacosmos
Learn how Pharmacosmos implemented Ennov Doc and Ennov QMS to become paperless and unify the organization
Ennov’s Medical Device Working Group Unites Industry Leaders
At Ennov, we believe in the power of collaboration to drive innovation. Our recent Medical Device Working Group session is a testament to this belief. This gathering of minds, featuring…
The Future of Medical Device Regulation: Insights from Ennov’s Expert Working Group
In an era where medical device regulation is becoming increasingly complex, the importance of robust regulatory compliance cannot be overstated. It’s a critical component that signifies not just adherence to…
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The New Wave of QMS [3/8]: Scalability
In the evolving landscape of the Life Sciences industry, growth and diversification are constants. From expanding into new markets, and developing innovative products, to integrating cutting-edge technologies, growth can take…
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The New Wave of QMS [2/8]: Comprehensive Integration
In an era marked by rapid technological advancements and increasingly interconnected business ecosystems, the call for seamless integration in Quality Management Systems (QMS) has become not just a desire but…
Strategic Safety Data Management for Cosmetic Compliance
The cosmetics industry is constantly changing, making safety data management a unique challenge. To adhere to global regulations, cosmetic companies need a versatile Cosmetovigilance (CV) system that evolves with the market. Choosing…
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The New Wave of QMS [1/8]: Setting the Stage for Modern Quality Management
In the Life Sciences industry, Quality Management Systems (QMS) serve as the cornerstone for ensuring product integrity, compliance with stringent regulations, and ultimately, patient safety. The landscape of QMS has…
Regulatory Compliance in the Cosmetics Industry
The cosmetics industry is subject to a complex array of regulatory frameworks that vary significantly across regions. In North America, for example, the FDA governs cosmetics under the Federal Food,…
Ennov to Sponsor 9th Annual European Drug Safety Pharma & Biotech Conference
Ennov is honored to announce that we are a Bronze sponsor of the 9th Annual European Drug Safety Pharma & Biotech Conference, a key event of the Pharmacovigilance World Tour.…
The RAP Up: Trends from 2023 RAPS Convergence
Now that we’re back from the RAPS Convergence in Montreal, I thought I’d share what stood out to me. While a number of interesting topics were discussed, what piqued my…
Ennov Forms Strategic Partnership with ION Pharma to Elevate Quality Management in Life Sciences
Ennov is pleased to announce a strategic partnership with ION Pharma. This alliance marks the beginning of a collaborative effort that merges over two decades of expertise in electronic Quality…
Ennov to Exhibit at the World Drug Safety Congress Americas 2023
Ennov is thrilled to announce our attendance at the World Drug Safety Congress Americas 2023, taking place at the Sheraton Boston, Boston, MA, on October 18-19, 2023. Meet Us at…
Ennov to Sponsor Global Pharmaceutical Regulatory Affairs Summit
Ennov is honored to sponsor the Global Pharmaceutical Regulatory Affairs Summit, a hybrid event taking place at the DoubleTree by Hilton, Brussels, from October 23-25, 2023. Accelerating Pharmaceutical Compliance with…
Navigating IDMP Compliance: The Time is Now
Navigating IDMP compliance can feel like an intricate puzzle with evolving guidelines, shifting timelines, and the complexities of data integration. Regardless, did you know, 41% of organizations are already actively…
The Future of Regulatory Affairs: Decoding the 2023 RAPS Convergence Agenda
As Life Science professionals, we often find ourselves at the crossroads of scientific innovation, compliance, and strategic business initiatives. Yet, how often do we pause to consider the transformative shifts…
Ennov to Exhibit at RAPS Convergence 2023
Ennov is thrilled to announce our participation at RAPS Convergence 2023, the largest and most well-recognized annual gathering of global regulatory affairs professionals. The event will be hosted at the…
Gartner Insights: IDMP & EMA Compliance
Navigating the labyrinth of pharmaceutical industry regulations, such as the Identification of Medicinal Products (IDMP) and European Medicines Agency (EMA) directives, demands an informed and authoritative approach. The challenge lies…
Ennov to Attend 2023 CDISC TMF Interchange
Ennov is excited to announce our participation in the 2023 CDISC TMF Interchange, a new annual conference dedicated to the TMF Reference Model Initiative and more, taking place at the…
Best Practices: Cross-Referencing in eCTD
Today, the eCTD format remains the only globally approved and ICH-recommended standard. While it has been in use for more than 15 years, it is the mandated submission format for…
Empowering Emerging Pharma Organizations through DLSP Strategy
The life sciences industry is rapidly evolving, and emerging pharmaceutical companies are at the forefront of this disruption. Companies leverage streamlined operations, nimble teams, and agile tech stacks to challenge…
Top 5 Trends in Life Sciences in 2023: Driving the Future of Innovation
The Life Sciences industry is undergoing a period of rapid transformation. As we progress through 2023, several critical trends have emerged, each presenting unique opportunities and challenges. Here are the…
Mastering Master Device Data: MDM Benefits for Compliance, Safety, Agility
For medical device companies, accurate and consistent data is critical for regulatory compliance and patient safety. Master Data Management (MDM) is an essential process that enables medical device companies to…
Ennov’s Agnostic Solution for IDMP, the EASI connector
Webinar Introducing Ennov's Agnostic Solution for IDMP, the EASI connector How are you going to be ready for IDMP compliance? Ennov has the answer.June 21st at 11:00 AM – 11:30…
Ennov to Exhibit at the 2023 DIA Global Annual Meeting, June 25-29 in Boston, MA
Ennov is set to exhibit at the 2023 DIA Global Annual Meeting, taking place June 25-29 in Boston, MA. Be sure to visit us booth #424! The DIA Global Annual…
PV-Signal Manager
Manage safety signals and demonstrate a robust approach to signal detection with a searchable repository and workflow-driven solution.
PV-Works Vet
Ensure veterinary safety with a flexible & compliant pharmacovigilance (PV) software. Manage data easily, meet critical reporting deadlines.
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