CyberActa is a boutique consultancy empowering medical device, digital health, and pharmaceutical companies in all their commercialization endeavors.
We draw upon our design, regulatory, technology, quality expertise, and the broad range of commercialization experience to advise clients on matters spanning the product life cycle, from product development and clinical trials to post-market compliance, privacy practices, software validation, and Quality System requirements in the US, UK, EU, Brazil, South Korea, Japan, and the rest of the World. Whether traditional medicinal products and devices or rapidly evolving medical and health technology products and services, such as SaMD or digital diagnostics and therapeutics, we have broad-based practical experience in advising clients to achieve approval and market acceptance.
We continuously seek out ways to improve and build a leaner, more flexible, and responsive approach by making use of innovative technologies and cutting edge, market-driven approaches to plan, organize and manage time and activities to deliver a high quality and efficient service, applying program and project management approaches to deliver operational excellence and creating the most appropriate and cost-effective delivery model for service in Product Development, Project Management, Regulatory Affairs & Compliance, Medical Device Cybersecurity Management, Privacy, Data Governance & Integrity, and Software Validation.
Our clients select the tailored strategic or tactical services at CyberActa because our services are effective, efficient, add value, and generate a sustainable and formidable competitive advantage.
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