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ISO 13485 Medical Devices

QualityMedDev is a platform for discussions about ISO 13485 and new standards and regulation for Medical Devices.

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Alec Alpert - Quality Assurance and Regulatory Compliance

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pkp.com.au
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mantrasystems.co.uk
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TS Quality & Engineering - Medical Device Consulting - TS Q&E - MDR
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Regulatory Pharma Net (RPN), founded in 1999, is a qualified Regulatory Affairs service and consulting company based in Italy. RPN highly-qualified team includes Regulatory Affairs, DrugDevelopment, Market Access and Pharmacovigilance Experts. RPN gives support during development, registration, launch and life cyclemanagement of Medicinal Products, Medical Devices, Cosmetics,Biocides and Food Supplements. RPN is partner of many pharmaceutical companies, managing hundredsof multitask projects, on a worldwide scale. We are proudly part of Pharos Healthcare Consulting, a new European Network of highly-specialised Market Access Strategic Consultancy. While maintaining each company’s independence and high local knowledge, we will be able to support Pharmaceutical companies in launching new drugs through our coordinated Market Access network across Europe, find out more at www.pharos-healthcare-consulting.com

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GMP Templates ISO 13485 and 21 CFR 820 for Medical Device manufactures and developers. Download your template now.

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