Discover how the FDA promotes the transition from CSV to Computer Software Assurance to improve software quality and optimize processes.
Navigating the HR landscape
With rapidly evolving human resources, this guide and platforms like V-Apps are essential for cutting-edge organizations.
Understanding FDA QMSR and ISO 13485 integration for medical device manufacturers
Discover how medical device manufacturers can meet FDA compliance by aligning with QMSR FDA and ISO 13485 standards using tools like eqMS.
ISO 13485:2016 and ISO 14971:2019 standards remain unchanged
L’Organizzazione Internazionale per la Normazione (ISO) ha annunciato che i diffusissimi standard ISO 13485:2016 e ISO 14971:2019 relativi ai dispositivi medici non subiranno revisioni al momento.
White Paper – IEC 62304 2nd edition insights
has officially released the 2nd draft edition of the renowned IEC 62304 standard for medical device software development.
White Paper – New Logistics contract combats illegal practices
Download our white paper and find out how the renewal of the National Collective Labour Agreement (CCNL) brings significant changes aimed at combatting illegal practices in logistics, handling, and freight forwarding activities.
White Paper – The critical role of Supplier Management in reducing risk and ensuring compliance
Download our white paper and explore in detail the importance of supplier risk assessment to ensure operational continuity, regulatory compliance, and commitment to sustainable and safe practices.
White Paper – Sustainability report: a practical guide for companies and SMEs
Download the white paper to transform the preparation of the sustainability report into a real engine of value and responsible growth.
White Paper – Construction Sites 4.0: Safety and Digitalization
The integration of access control software can improve transparency and compliance with regulations.