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Thank you for considering NovintiX. We're excited to collaborate with you.
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Whether you're exploring a new project, looking to improve existing processes, or seeking expert guidance on regulatory compliance—we're here to help you succeed.
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Common Questions
What industries do you serve?
We specialize in medical devices, biotechnology, pharmaceuticals, and digital health solutions, serving clients across the healthcare ecosystem.
How quickly can you start a project?
Depending on scope and resource availability, we can typically begin new engagements within 1-2 weeks of contract finalization.
Do you offer remote collaboration?
Yes, we have extensive experience with distributed teams and offer flexible engagement models including on-site, remote, and hybrid arrangements.
What regulatory standards do you work with?
We're experienced with FDA, CE marking, ISO 13485, ISO 14971, IEC 62304, and other relevant medical device and pharmaceutical regulations.