5 Ways Errors Slip into Your Salesforce Production Environment – And How to Avoid Them
Salesforce is a double-edged sword. On one hand, its level of usability and ease of customization have allowed teams to modify the CRM to fit their exact needs. On the other, changes made by citizen developers can have unanticipated downstream effects that surface as defects in your production environment, bringing productivity and progress to a halt.
Read this white paper to learn:
- 5 common ways errors slip into production.
- How to spot potential points of failure before changes are deployed.
- How test automation can minimize risk and ensure that new releases do not impact your existing org.
Minimize Salesforce Bugs and Maximize ROI
Salesforce is designed to democratize innovation by empowering users to generate their own customizations through its low-code platform. Without a doubt, Salesforce is an intricate and vital piece of your organization’s digital modernization puzzle, as it’s connected to many of your critical business apps through backend flows.
Salesforce makes its platform as easy to maintain as possible. The company thoroughly tests its three yearly releases, but it’s up to customers to verify that their customizations, integrations, and applications built on the Salesforce platform work as intended.
Digital Validation: Achieving Modern Compliance for Modern Testing with Tricentis Vera™
Join us to see how modernizing compliance with Tricentis Vera™ to support digital validation for life sciences. In this webinar you will learn:
- How Tricentis Vera™ helps you meet business objectives while satisfying compliance requirements.
- How shifting to digital validation supports quality, not documents.
- How you can easily implement electronic signatures, automated review and approvals process, and technical controls across the development and testing toolchain.
- Modernize software compliance in life sciences.
- Enhance CSV lifecycle with digital validation.
- Adopt compliance for Agile testing.
Agile, Digital Validation: How to Modernize Software Testing for Life Sciences
Remain competitive and compliant when adopting a digital approach to validation. Uncover important industry trends life sciences organizations must address, such as:
- Why a modernization strategy is needed in regulated software testing, and how adopting digital, data-driven approach with Tricentis Vera™ addresses this need in Computer System Validation today.
- The industry trends influencing modernization in computer systems validation.
- The advantages of adopting an Agile, digital approach to validation.
- The limitation of document-based approaches for review and approval.
- Modernize software testing for life sciences.
- Why life science companies choose Vera™ to lower costs and increase efficiency.
Best Practices for Computer Systems Validation in The Digital Age
Negotiate changes with computer systems validation best practices to get ahead of increasing demands around digital transformation. Learn valuable tips for negotiating changes with computer systems validation, such as:
- Important steps to plan, develop, manage, and control your computer systems validation program.
- List of best practices to help implement an effective, scalable software compliance program that supports digital transformation initiatives.
- Minimize risks, reduce cost, and avoid common pitfalls.
- Reduce the costs, risks, and complexities of compliance.
- Plan an effective and efficient CSV program.
- Key mistakes to avoid with computer systems validation.
