With us you stay compliant and innovative despite regulatory requirements
Navigating compliance in life sciences: Increased demand for digitalization increases the need for lean but compliant computerized systems validation.
In the life sciences industry, meeting diverse requirements, from customer demands to strict adherence to laws, standards, and guidelines, is crucial. At BearingPoint, we understand the complexity imposed by regulations such as GxP, FDA 21 CFR Part 11, ISO 13485, MDR, and IVDR. Part of that encompasses validating computerized systems, including ERP systems, and the qualification of the underlying IT infrastructure. Our clients face a variety of questions that require flexible solutions and approaches. BearingPoint, together with you, will find lean, compliant, and business-oriented answers.
Our clients must ensure that computer systems in regulated areas, such as pharmaceuticals, medical devices, healthcare, and life sciences, meet regulatory requirements and operate reliably. Several challenges are associated with computerized systems validation, from digital transformation to reconciling compliance and innovation. Rapid technological advancements present challenges in validating and maintaining compliance with newer systems. Adapting validation processes to emerging technologies like cloud computing, artificial intelligence, and the Internet of Things (IoT) can be particularly complex.
We assist clients in finding customized solutions by leveraging our profound expertise in consulting and providing relevant products to address their challenges effectively. Our goal is to facilitate computerized systems validation to help our clients focus on what is essential: their patients’ health.
In a rapidly evolving industry, we consider ourselves to be a facilitator for compliance. Join us on a journey that aligns innovation with compliance, the future of the GxP-regulated industry.
Join us in facilitating compliance to ensure your patients’ safety. Contact us today.