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INDIGO GLOBAL CONSULTING GROUP. Regulatory, Quality and clinical Services. Medical Devices, Combination Products, IVDs, Pharmaceuticals & Nutraceuticals. US and Global Regulatory Strategies. Quality System Design Clinical Trial Management. PMA, 510(k) & NDA Submissions Internal & Supplier Audits OUS Clinical Trial Support. OUS Technical Submissions ISO 13485 Certification Readiness Investigation Medical Devise Dossier. INDs and IDEs FDB Drug and Medical Device Licensing Clinical Site Audits.

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INDIGO GLOBAL CONSULTING GROUP. Regulatory, Quality and clinical Services. Medical Devices, Combination Products, IVDs, Pharmaceuticals & Nutraceuticals. US and Global Regulatory Strategies. Quality System Design Clinical Trial Management. PMA, 510(k) & NDA Submissions Internal & Supplier Audits OUS Clinical Trial Support. OUS Technical Submissions ISO 13485 Certification Readiness Investigation Medical Devise Dossier. INDs and IDEs FDB Drug and Medical Device Licensing Clinical Site Audits.
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INDIGO GLOBAL CONSULTING GROUP. Regulatory, Quality and clinical Services. Medical Devices, Combination Products, IVDs, Pharmaceuticals & Nutraceuticals. US and Global Regulatory Strategies. Quality System Design Clinical Trial Management. PMA, 510(k) & NDA Submissions Internal & Supplier Audits OUS Clinical Trial Support. OUS Technical Submissions ISO 13485 Certification Readiness Investigation Medical Devise Dossier. INDs and IDEs FDB Drug and Medical Device Licensing Clinical Site Audits.

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