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At Mittal Consulting, we take charge of all regulatory tasks from product development to approval. This service is pivotal for ensuring your medical device aligns with regulations, facilitating efficient market entry. Here's a snapshot of what our Regulatory Project Management includes:

  • Project Planning
  • Regulatory Strategy (e.g., 510(k), PMA, CE Marking)
  • Regulatory Submissions
  • Communication with Regulatory Authorities
  • Risk Management (ISO 14971)
  • Training

With Mittal Consulting, your regulatory journey is seamlessly managed, guaranteeing compliance and a streamlined path to market.