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Found 14 results for the keyword pmcf. Time 0.005 seconds.
Post Market Clinical Follow Up (PMCF) Consulting - MakroCareComprehensive PMCF planning and post-market clinical follow-up (PMCF) solutions for medical devices. Your trusted PMCF partner.
Medical Devices Clinical Trial Management l PMCF CRO - MakroCareMakroCare offers Clinical Trial Management for Medical Device and Clinical Monitoring CRO services to Biopharma and Medical Device companies.
Medical Device CRO l Clinical Vendor l Clinical Consultant - MakroCareMakrocare Provides CRO Clinical Vendor and Clinical Consultant Services to Biopharma and Medical Device Companies. we make sure that your product complies.
Regulatory, Clinical Consulting Services to Biopharma Medical DeviceMakroCare is a leading clinical research organization (CRO) and regulatory affairs consulting firm providing expert services to the life sciences industry.
Performance Evaluation Report (PER) | IVDR PER - MakroCareFrom IVDR perspective, clinical evidence should support the intended purpose of a device as stated by the manufacturer and that is based on performance evaluation. This is guided by a performance evaluation plan (PEP), a
Regulatory Authorized Representative for Medical Device - FDAMakroCare offers Regulatory Authorized Representative services FDA authorization for Medical Device in the USA and UK. We make sure your product complies.
Medical Device Registrations Dossiers - MakroCareOur global Medical Device Regulatory experts are well experienced in registrations and technical files management for regulatory authorities.
Regulatory Strategy for Medical Devices - FDA ConsultingMakroCare helps Medical Devices Diagnostic companies with professional FDA consulting and regulatory strategy. Trust MakroCare for an effective FDA consulting.
Medical Device QMS Consulting and SOP Management - MakroCareMakroCare can create processes and Quality Management Systems that ensure the quality of your processes leading to fewer worries when the next audit
Clinical Evaluation Report (CER) for Medical Devices - MakroCareMakroCare help you ensure that your Clinical Evaluation Report (CER) meet strict new requirements of Rev 4 and the European Medical Device Regulation (MDR 2017/745) and MakroCare will assist you in completion of your CER
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