Strategic alliances: how to expand the perception of value in complex markets
Product design centered on compliance: How to create scalable solutions for regulated markets
NR 7: What it is, how to adapt your company, and avoid fines [Step-by-step guide]
Strategic alliances: how to expand the perception of value in complex markets
In technical and regulated markets, the excellence demanded by customers, suppliers, and regulatory bodies demands more than just isolated solutions. In this scenario, creating deep alliances transforms the business ecosystem itself, expanding the perception of value for all stakeholders.
Product design centered on compliance: How to create scalable solutions for regulated markets
Product design centered on compliance transforms regulations into competitive advantage. Discover how modular frameworks and AI create scalable, user-friendly solutions for regulated markets.
NR 7: What it is, how to adapt your company, and avoid fines [Step-by-step guide]
The essential guide to Regulatory Standard 7 of the PCMSO. Understand what the regulation is, its legal obligations, required medical exams, and the step-by-step compliance process. Avoid fines!
ISO 42001: All about the new standard for Artificial Intelligence
ISO 42001 (also known as IEC 42001) is an international standard that sets standards for the adoption of an Artificial Intelligence Management System (AIMS). Although it is not mandatory, it is widely used in the market because it allows companies to create, implement, maintain, and continuously improve Artificial Intelligence management. In this way, the ISO 42001 standard ensures that AI tools are used responsibly, reliably, transparently, and ethically.
Energy Management System: How to choose the best software for your company
Discover how to choose the ideal energy management system to reduce costs, ensure ISO 50001 compliance, and turn regulatory pressure into a competitive advantage. Strategic guide!
Are you ready for Directive 2023/1791? See if your company is in the crosshairs
Is Your Company Ready for EU Energy Efficiency Directive 2023/1791? Discover Obligations, Deadlines Until 2027, and Penalties for Non-Compliance. Learn 7 Steps to Implement ISO 50001 and Turn Compliance into a Competitive Advantage.
Electronic Document Management (EDM) in 2025: integrated, intelligent, and predictive
Electronic document management in 2025 cuts costs and risks with predictive AI, D4Sign e-signatures & LGPD/GDPR compliance. Turn documents into strategic assets!
How file management software can go beyond just storing items
File management software allows you to store documents, track versions and audit trails with traceability, and manage configurable permissions per user. With all this, it is possible not only to store items but also to act collaboratively in real-time with secure access between different sectors of a company.
RDC 658/22: good manufacturing practices for medicines
A RDC 658 dispõe sobre as diretrizes gerais de Boas Práticas de Fabricação (BPF) de Medicamentos no Brasil. Publicada em 30 de março de 2022 pela Diretoria Colegiada da Anvisa, ela revogou a resolução anterior de 2019, que já tinha sido um marco para a categoria. Na prática, a RDC 658/22 não modifica o entendimento … <a href="https://blog-cms.softexpert.com:8080/en/rdc-658-22-good-manufacturing-practices-for-medicines/" class="more-link">Continue reading<span class="screen-reader-text"> "RDC 658/22: good manufacturing practices for medicines"</span></a>