Templates save you significant time and effort costs when getting started with Intland’s software solutions. They enable you to implement our solutions fast, and can dramatically reduce the costs of regulatory compliance.
Our templates come with predefined artifacts, workflows, and baked-in domain knowledge out of the box. Need to adapt the template to your needs? Rely on Intland’s consulting services to help you custom-configure these generic templates to your specific use case.
- Use templates out of the box, and realize value from day one
- No programming or scripting experience needed
- Take the headache out of regulatory compliance
- Tailor predefined templates to your teams’ needs with minimal effort
- Accelerate safety-critical audits and simplify regulatory compliance
codeBeamer ALM Templates
Intland’s Automotive ISO 26262 & ASPICE Template was designed to help you achieve compliance with the international standard ISO 26262, and adhere to the requirements of the Automotive SPICE and CMMI models. The template, which leverages the capabilities of codeBeamer ALM, enables you to develop safety-related embedded automotive systems up to ASIL D or SIL 3.
Intland’s Avionics DO-178C & DO-254 Template provides out of the box support for compliance with the requirements of avionics standards DO-178C and DO-254. The template was designed to help developers of avionics embedded systems ensure the quality, safety and reliability of their airborne products. It contains preconfigured work items, and allows you to specify and enforce the use of compliant avionics development processes.
Intland’s Pharma GAMP® 5 Template supports the application of a risk-based approach to the management of compliant GxP computerized systems. It helps pharma companies, suppliers, and system integrators ensure that the systems used in pharma projects are fit for intended use, and comply with the requirements of the Good Automated Manufacturing Practice® 5.
Intland’s Scrum Template (included with codeBeamer ALM out of the box) was created to support teams working under the Agile framework with Scrum and Kanban. It offers various features to support Agile development, providing a great basis for any Agile project.
Agile/Scrum and Waterfall/V-model seem to be methods with really different fundamentals, but they may be complementary for complex, multi-tier system development. In most cases, hardware components are developed using a Waterfall/V-model method, while the development of software components can be managed with an Agile approach. Intland’s Agile-Waterfall Hybrid Template (included with codeBeamer ALM out of the box) is able to support both of these, as well as the combination of Agile and Waterfall in a custom Hybrid method.
Scaling Agile across large organizations is a difficult task. For enterprises looking for a safe and smooth way to transition to Agile, one that lets them keep organizational structure and control over their teams, the Scaled Agile Framework (SAFe®) is a great solution. As the first implementation of the Scaled Agile Framework in the Agile world, Intland’s SAFe® Template offers a dedicated template that supports adherence to this complex framework, and enables you to manage and monitor the work and performance of multiple Agile Release Trains in a convenient, easy to overview manner.
Intland Retina Templates
Use this template to manage your medical device software design and engineering processes from requirements all the way through to validation. Take advantage of built-in medtech development knowledge to adopt best practices with minimal effort. Use the template to ensure compliance with EU MDR and US FDA regulations and applicable standards: IEC 82304-1, IEC 62304, ISO 14971, and FDA 21 CFR Parts 11 & 820.
Use this template to ensure high product quality and accelerate regulatory audits. Control quality documents, manage eForms and CAPA, and conduct Root Cause Analysis all in one place. Adhere to regulatory requirements, simplify compliance assessments, and tackle compliance audits for QMS regulations including ISO 13485:2016 and FDA Title 21 CFR Part 820. Rely on this template to maintain rigorous quality control across the entire development lifecycle, to manage deviations from established processes, and to report on your quality activities in order to simplify audits.