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ISO 13485:2003 Expert Witnesses testifying in Litigation

ISO 13485:2003 experts in this Medical Devices directory provide witness opinion and testimony in all types of ISO 13485:2003 situations.

In litigation, ISO 13485:2003 experts attempt to use forensic research and years of professional experience and research to reconstruct the incident and damages or event by providing witness testimony, to opine in a compelling way to the jury

Medical Devices Expert Witnesses for Attorneys

Search results for: ISO 13485 2003

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State: CT
Region: Eastern, Northeast
Country: US

Provides Opinion & Testimony In:
Regulatory Affairs, Clinical Affairs, Quality Assurance, Regulatory Compliance, Medical Device, Combination Product, Design Dossier, Medicinal Dossier, Director, Client Manager, Project Manager, 510(k),515i, Pre IND, IND, Pre IDE, IDE, HUD, USAN, HDE, PMA, Pre Sub, Recall, Correction, CTA, FDA, CDRH, CE, OUS, MAF, Pre submission, Pre IDE, De Novo, Recall Correction, Appeal, Supplement, Annual report, FSN, FMEA, CER, FSCA, MDEL, MDR, 13485, 10993, 14971, 60601, CMDR, PMS, PMCF, NCA, EFTA, Apostille, legalization, CFG, CFS, QMS, QC, 21 CFR 820, 21 CFR 801, 21 CFR 803, MDL, 21 CFR 807, MEDDEV, NB, Product Liability, Infringement, Patent Infringement, Injury law,CE, TUV, Intertek, SGS, DGM, NSAI, SNCH, BSI, UL, Medicinal Consultations, MHRA, MPA, ETAT, License Applications, Health Canada, TGA
Click to view this experts CV View CV for Regulatory Marketing Compliance Quality Assurance Medical Device Expert Witness No.3571Click to request this expert Request This Regulatory Marketing Compliance Quality Assurance Medical Device Expert Witness No.3571

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