Founder and principal consultant of this consultancy specializing in project roles for medical device manufacturer and pharmaceutical companies in the following areas:
•	FDA compliant Non-Conformance management, Deviations, purchasing controls, global supplier quality & development including quality assurance (extensive experience in managing and executing remediation or work stream activities related to 483 citation, Recall or Consent Decree)
•	CAPA/SCAR system management 
•	FDA compliant medical device complaint handling business process 
•	Process Improvement (business & technical)
•	Supply chain improvements (diagnostic, analysis and recommendations)
•	Biosensor (strip) technology resolution, development & transfer 
•	Manufacturing technology development & transfer 
•	Due-diligence (product, process & supply chain)

For more details, please visit ravibhullar.com 

*   Technology Development & Transfer -Special expertise in disposable biosensor-glucose strips (optical and electrochemical) product design and manufacturing technologies.

*   Medical device complaint Management Process per FDA requirements, ( per QSR 21 CFT 820.198) 

*   Continuous Process Improvement & Lean Initiative Implementation (Cost Reduction, Efficiency Improvement, Accuracy Improvements, Eliminating Non-Value-Add Activities, Automation and Compliance Management)

RAVIBHULLAR, LLC

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RAVIBHULLAR, LLC

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