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    Minoti Patel, RAC (US)
    Manager, Regulatory Affairs at Thermo Fisher Scientific
    July 2015
    Complaint Handling - Complaint or Not?
    Joe Hage
    🔥 Find me at MedicalDevicesGroup.net 🔥
    April 2013
    ISO13485 requirements on component parts
    Saurabh Dubey
    Regulatory Affairs & Quality System
    November 2018
    EU MDR Article 22
    Rob Packard
    Ship & Print Your FDA eCopy
    March 2017
    Is a DHF Required for a Class I Device?
    Rob Packard
    Ship & Print Your FDA eCopy
    October 2015
    How to write a clinical evaluation report (CER) for CE Marking
    Antonia Trevisan
    regulatory engineer presso Lima Corporate
    August 2018
    MDR: Are custom-made devices exempt from CE marking?
    Joe Hage
    🔥 Find me at MedicalDevicesGroup.net 🔥
    July 2019
    The Innovation Every Ostomy Patient Needs
    Joe Hage
    🔥 Find me at MedicalDevicesGroup.net 🔥
    February 2019
    $350 worth of free advice about reimbursement
    Aurélie HOUEL
    Directeur Assurance Qualité / Responsable Affaires Réglementaires Sécurité Produits chez SEPPIM SAS
    September 2015
    Autoclave with no drying cycle - what is the consequence on sterilization state during the storage?
    Eyal Lerner, Ph.D., B.Pharm, ICQE
    Pharmaceutical Quality Consultant [email protected]
    March 2018
    Was Theranos approved by CSM, FDA or both?
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