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Search Results (13)
Type: Conference
Date: 2017-09-19
Duration: 3 days
Location: Sottsdale Plaza Resort, AZ
Registration: More Information
The Omnify Software User Conference provides an opportunity for Omnify Software customers and partners to experience an unparalleled training event over the course of two days. From beginner to seasoned-there is training for every level of user.
Omnify customers who attend the conference will gain in-depth product training, learn best practices from peers and access takeaway material to share with their team.
The Omnify Software User Conference is provided free of charge for current Omnify Software customers and partners.
Type: Seminar
Date: 2017-05-08
Duration: 3 Days
Location: San Jose, CA
Registration: Register Online
The IEEE Product Safety Engineering Society hosts a premier symposium annually on all relevant topics for workers and innovators in the product safety area. The symposium offers 3 days of technical sessions and exhibits.
Compliance Dynamics, an Omnify Software partner, will be presenting on the topic of "Creating efficient business processes for compliance".
Visit booth #7 to see a live demo of Omnify Empower PLM and learn how it can support your product compliance initiatives.
Type: Webinar
Date: 2017-04-06
Duration: 45 minutes
Location: Online
Registration: Registration Closed
Small and Mid-sized Businesses (SMBs) have many compliance requirements levied upon them by regulators, industry, and customers. SMB manufacturers have the difficult job of interpreting each requirement and deciding when compliance is enough, and when additional investment and effort are warranted. One such requirement is ISO 9001 – the quality management backbone for many manufacturers – and the new ISO 9001:2015 update. ISO 9001 is a contractual requirement for certain industries and customers, and SMB suppliers to these industries and customers must be re-certified to ISO 9001:2015 by October 2018.
Type: Demonstration
Date:
Duration: 1 Hour
Location: Online
Registration: Register
See the latest version of Omnify Empower PLM in action and join our interactive question and answer sessions
Type: On-Demand Webinar
Date:
Duration: 26 Minutes
Location: Online
Registration: View Recording
Transitioning from a paper-based document control and change management process to an electronic system can be a bit intimidating, particularly for regulated medical device companies. If your company considered moving to a more efficient electronic product development process to manage BOMs, ECOs, Documents and Quality data but hesitated because of concerns about meeting compliance or weren''t quite sure where to begin or what to do, check out this webinar.
This webinar provides an overview on why and how a medical device client transitioned from a paper-based product development process to an electronic Product Lifecycle Management (PLM) system. Guest speaker, Joseph Ko, Director of Quality for Autonomic Technologies (ATI) shares best practices and the three steps his company took to achieve an FDA and ISO compliant implementation.
Topics covered include:
  • Paper-based development process pitfalls
  • Why ATI chose to automate
  • Why ATI chose PLM
  • Things to be aware of as a medical device manufacturer
  • Three steps to a compliant implementation (prototype phase, validation phase and migration phase)
  • Keys to a successful implementation
This webinar will provide an overview of the timeline and resources needed for ATI's implementation as well as an overview of the entire validation project including: planning, risk management, FDA Part 11 compliance, requirements, and verification protocols.
Type: On-Demand Webinar
Date:
Duration: 42 Minutes
Location: Online
Registration: View Recording
Are your Bill of Material (BOM) and Engineering Change processes driven by paper management, spreadsheets, documents, small databases, or a combination?
If your company is among those that still manage product data with manual processes, you will want to view this webinar. Manual processes can result in inaccurate data, duplicate efforts, re-work and overall wasted time. It is important to have the right tools in place to get the job done effectively and efficiently.
Learn how to assess and address your paper BOM and Change Management processes. You will have a better understanding of the benefits and improvements an automated system can deliver and how to implement best practices that fit your company.
Presented by Charity Perillo, Independent Consultant, this webinar covers:
  • Assessing your current BOM, Change and Document Management environment
  • How to leverage technology to automate and improve processes
  • Moving from legacy to automated practices-ensuring a smooth transition
  • The human element; how moving from paper to electronic affects employees
Type: On-Demand Webinar
Date:
Duration: 42 Minutes
Location: Online
Registration: View Recording
This webinar provides clarification on the differences between ERP and PLM, where they fit in the product development and manufacturing process, and how integrating these environments can deliver positive results.
Guest speakers from Treske Precision Machining provide a detailed overview of the integration of their ERP and PLM systems, what information is shared, process improvements they have realized and a demonstration of their integration.
This webinar covers:
  • Overview of ERP and PLM (What's the Difference?)
  • Automated data sharing as a best practice (engineering changes, BOMs, AVLs/AMLs, costs, lead times, etc...)
  • How to keep design and manufacturing in sync
  • Case in point demonstration from Treske Precision Machining
Type: On-Demand Webinar
Date:
Duration: 22 Minutes
Location: Online
Registration: View Recording
This presentation was given during the MedTech Cardio conference and discusses developing and utilizing information-sharing platforms such as Product Lifecycle Management (PLM) to promote cross-functional collaboration and innovation and avoid “reinventing the wheel” in multiple product lines.
This webinar covers:
  • Leveraging technology to promote sharing of ideas for cardiovascular and other medical device innovations
  • Best practices for efficient collaboration among engineers, scientists, manufacturing, etc.
  • Tracking product information to avoid duplicating efforts and improve resource efficiency
  • Managing information for quality and compliance
Type: On-Demand Webinar
Date:
Duration: 34 Minutes
Location: Online
Registration: View Recording
This webinar is based on a client interview and addresses the top ten questions many organizations have about adopting an automated Quality Management System.
You will hear from a Sr. Quality Engineer on his experience with implementing a PLM-based Quality Management system to address ISO 9001 compliance requirements.
Type: On-Demand Webinar
Date:
Duration: 40 Minutes
Location: Online
Registration: View Recording
FDA and IEC requirements for validation of your manufacturing and quality system software can conjure up a lot of questions. Understanding the actual guidelines and best practices for meeting these requirements isn't always clear.
This educational webinar provides answers the top five software validation and documentation questions asked by others in FDA regulated industries and demonstrates best practices for meeting the guidelines.
This webinar covers:
  • Why documentation is important
  • What documentation is required for regulatory validation
  • How to upgrade a validated system
  • Best practices for meeting and maintaining compliant processes
Type: On-Demand Webinar
Date:
Duration: 45 Minutes
Location: Online
Registration: View Recording
Today's supply chain is more complex than ever. How are companies efficiently managing supply chain data to ensure accuracy and compliance?
View this educational webinar to learn how to improve Supplier Management efficiency by adopting best practice guidelines such as APQP and PPAP, centralizing supplier information and managing data electronically.
This webinar covers:
  • Compliant Supplier Management requirements and challenges
  • Adopting APQP and PPAP as best practice processes for compliant Supplier Management (not just for automotive anymore!)
  • PLM for Supplier Management-creating centralized and automated supplier data management (automate AVL/AML management, forecast materials, access management dashboards and reports)
  • Demonstration of PLM software as the technology backbone for compliant Supplier Management processes
Type: On-Demand Webinar
Date:
Duration: 45 Minutes
Location: Online
Registration: View Recording
FDA statistics show that 45 to 50 percent of all device recalls stemmed from poor product design. Design controls are not only a regulatory requirement, they lay the foundation for the proper design and development of medical devices and can provide device manufacturers with the opportunity to address and/or correct problems early in the design process.
Learn how to implement effective and efficient product development procedures with Product Lifecycle Management (PLM) technology in order to ensure compliant design controls, address design control challenges, simplify the audit process, and reduce the cost of compliance through automated enterprise resource systems and best practices.
This webinar covers:
  • ISO and FDA Design Control requirements
  • Compliance documentation requirements
  • Recommendations to effectively meet the requirements of Design Control
  • Integrating Design Controls into the business of best in class New Product Development (NPD)
  • Demonstration of PLM technology supporting best practice Design Controls
Type: On-Demand Webinar
Date:
Duration: 29 Minutes
Location: Online
Registration: View Recording
RoHS, the RoHS Recast and the impending Conflict Minerals directives have greatly impacted manufacturers. As an organization required to meet these regulatory guidelines, do you have the proper data management tools and processes in place to comply?
View this educational webinar with guest speaker, Mike Shannon, the Director of Hardware Shared Services at Avid where Mike will discuss the value of creating a central data driven system to manage compliance information and address compliance early in the planning and design of new products.
This webinar covers:
  • Brief overview of RoHS, the recast and Conflict Minerals
  • Being compliant and what it means to your product developers
  • How to manage data for RoHS, Conflict Minerals and CE Technical Files
  • Approaches for outsourced Contract Manufacturing partnerships
  • Best practices for meeting and maintaining compliant processes