On Demand Webinars

On Demand Webinars


Revolutionizing Validation & Compliance: Unleash the Power of AI Using CIMCON’s Validated AI Agent Suite

Life science companies invest major resources in validation and compliance. Though Agentic AI can significantly reduce these costs, a lack of sufficient AI talent and validation concerns have hindered their adoption.

Leveraging its 25 years of experience in validation and compliance, CIMCON has developed a revolutionary Agentic AI platform that provides an end to end solution that includes:

  • A libary of pre-built AI Agents for validation, gap assessments and much more that can be put to immediate use – no AI knowledge required!
  • A suite of tests for validating AI agents, GenAI, LLMs and AI models that comply with the FDA AI Guidance
  • A 21 CFR Part 11 compliant , end to end AI Lifecycle Platform for Inventory, Discovery, Change Control, Use & Validation of AI models

oin CIMCON in this webinar to learn how you can convert the hype into reality and reap the benefits of Compliant AI™ in your organization.

 

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Automating AI Model Validation and Complying with the FDA Guidance on Artificial Intelligence

The FDA recently issued a draft guidance on AI in January 2025. The guidance provides recommendations on the use of AI to produce information or data that supports regulatory decision making regarding the safety, effectiveness, or quality for drugs.

Learn more about this guidance, and review how CIMCON’s AIValidator™ and EUC Insight™ software provides you with a proven and mature end-to-end AI Risk Management Platform that automates model validation and compliance with the FDA guidance.

 

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Audit Trails and E-Signatures for Your Spreadsheets

21 CFR Part 11 Compliance in Seconds

Add audit trails and e-signatures to your spreadsheets in seconds using CIMCON’s eInfotree Excel Desktop Software. Trusted by hundreds of regulated firms for over 20 years, eInfotree makes your spreadsheets 21 CFR Part 11 compliant. Additionally, the XLValidator software helps you validate spreadsheets by automatically generating validation documents.

The use of compliant spreadsheets are endless – as a form, a calculator, or to capture e-signatures. No more re-calculating or printing and signing paper copies!! Start your Digital Transformation Journey with spreadsheets!

In this webinar, learn how you can achieve data integrity for your spreadsheets with just a few clicks, minimal user training, or changes to your existing process.

 

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Simple and Easy to Use Quality Management System

Using a Seamless On-Premise or SaaS Solution

Replace your paper, spreadsheet or disparate document/training processes with a single integrated system. Reap the benefits of digital transformation with electronic signatures, faster review and approvals, and a seamless training process where a new SOP revision automatically triggers new training requirements, that can be met using self-training and training assessments.

 

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Achieve Lab Excellence by Optimizing Operations and Enhancing Data Integrity, Security and Compliance

Fragmented and disparate lab applications are a major barrier to optimize operations and a significant source of data integrity issues. As such, they represent the “last mile” of Digital Transformation.

Attend our free webinar to learn how you can achieve lab excellence by integrating all lab applications into a centralized system, implement security, automated data backups and workflows, audit trails and e-signatures, resulting in significant productivity and compliance benefits.

 

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Automatically Migrate Your Existing Paper Forms to Electronic

Convert your existing paper-based forms in Word, Excel or PDF format to Part 11 compliant electronic forms automatically without having to recreate them!!

Eliminate the effort required with printing, filling, signing and storing paper forms to realize significant time and cost savings using CIMCON’s smart and Compliant Digital Transformation technology. Join us in this webinar to learn how CIMCON’s Transform software can help you reap the following Additional Benefits:

  • Control data quality at point of entry with validation rules
  • Apply E-Signatures
  • Route for Review/Approval
  • Store Form Data for Searching, Reporting, Analysis and Integration
  • 21 CFR Part 11 Compliant

 

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eCADinfo Engineering Data Management System

Demonstrate eCADinfo Engineering Data Management Solution.

Additional Benefits:

  • Gain an in-depth understanding of the 21 CFR Part 11 compliant eCADinfo
  • Engineering Data Management Solution with integrated modules to track changes to AutoCAD drawings and Excel spreadsheets
  • Route for Review/Approval
  • View a demonstration of the software in a recorded, web-based, no obligation seminar
  • An Internet connection and computer speakers are all you need

 

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