Johner-institute ทางเลือก & คู่แข่ง
The Johner Institute supports medical device manufacturers in the standard-compliant and efficient development of their products and the establishment of QM systems through consulting, seminars, books and video trainings.
ทางเลือกและคู่แข่งของ johner-institute.com ในแง่ของเนื้อหา การจราจร และโครงสร้าง
Keep Calm and start creating your MDR Transition Plan - Medical Device Regulation.
Oriel STAT A MATRIX has been a global leader in medical device and IVD quality and regulatory consulting, auditing and training since 1968.
I3cglobal.com is ranked number 10M in the world.
The leading MedTech Services provider, offering Medical Device Consulting, clinical trial, lab & reimbursement services to support the entire product lifecycle.
The European Union Medical Device Regulation – Regulation (EU) 2017/745 (EU MDR).
Learn about the first and only holistic Regulatory Information Management (RIM) software for medical device companies that consolidates all the functions of regulatory affairs.
Ensure 100% medical compliance. Decomplix does your CE certification for medical devices and IVD in the pre- and post-market phase. Learn more here.
Want to Master Medical Device Regulation & learn how to put a product on the market in Europe. Easy Medical Device is a platform for tools and resources for Regulatory Affairs, Quality Management, Regualtory Compliance. Learn how to choose your notified body or how the device regulation is different in other countries
Der Regulatory Affairs Blog für alle Themen rund um die internationale Zulassung von medizintechnischen Produkten.
The ISO 13485 Store provides instructions, materials, and services for your organization to become certified in the ISO 13485 Quality Standard.
Qserve is your MedTech Consultant for Regulatory Affairs & Quality Assurance and Clinical Trials. Need regulatory advice, support or training? Contact us.
Germany based EU Authorized Representative "mdi Europa" helps small to medium sized manufacturers to enter european medical device market.
Cite Medical Solutions is the leader in EU MDR (medical device regulatory) consulting, high-quality literature search, and post market surveillance systems. Contact today!
Celegence provides you with leading life sciences regulatory solutions & services for medical writing, medical device regulations, labeling, IDMP and more.
The Regulatory Writing Experts
Regulatory Globe offers Expert Regulatory Affairs strategies and helpful implementation tools for medical devices. Stay updated with EU MDR, IVDR and more.
Medical Device consulting services - regulatory and quality - FDA, CE marking, ISO 13485, MDSAP, biological and clinical evaluation.
Das Johner Institut unterstützt Medizinprodukte-Hersteller bei der normenkonformen und effizienten Entwicklung ihrer Produkte und dem Aufbau von QM-Systemen durch Beratung, Seminare, Bücher und Videotrainings.
Freyr provides Regulatory Software, Automation and Digital Transformation Solutions to Lifesciences companies across the globe.
Advena Ltd – EU Regulatory & Quality Consultants for Medical Devices & Cosmetics.
Lne-america.com is ranked number 1985982 in the world and links to network IP address 205.134.253.67.
Internal & lead auditor training, IRCA approved experts for over 50 years. Specialists in ISO 9001/14001, OHSAS 18001, ISO / TS 16949, AS 9100.
Naveen Agarwal on technology in Healthcare. Build and improve Quality Systems to fuel business growth. Covering FDA Risk Management, Quality Systems Regulation, FDA Medical Devices, Regulatory Compliance, NLP in Healthcare, Healthcare Quality Solutions, Medical Device Risk, and MedTech News.
EUDAMED services: EUDAMED UDI submission software, EUDAMED consultancy, training, and MDR, MDD, IVDD, AIMDD, SPP & IVDR EUDAMED device templates
RCA Inc. has global regulatory & compliance expertise for medical device, pharmaceutical, biologics, combination products and compounding pharmacies.
Experts in Clinical Research and Regulatory Services for MedTech and IVD Industry. Optimize your clinical trials with AKRN Medical Device CRO.
Our team of Medical Device Regulatory Consultants are specialists offering tailored EU MDR Compliance services.
Learn more about Network Partners, a medical device and pharmaceutical consulting and contract staffing agency providing packaging engineering, regulatory affairs, labeling, cold chain solutions and project management.
Alysidia is solution provider for Blockchain, Cloud, IoT, AI, RFID integration for Supply Chain, Eudamed, UDI, e-IFU, e-QMS for the Medical Device & Pharma field
Clinical Evaluation Report | Number one source for Clinical Evalution Reports.
Freyrtechnology.com is ranked number 10M in the world.
Agatha provides intelligent document management applications for life sciences companies including clinical trial management, quality management, regulatory management and standard operating procedures
GreatFour Systems is one of the leading enterprise software company for Packaging, Labeling, Proofing, Regulatory and Project Management solutions.
GxP-konforme Software der Digital Life Sciences GmbH. Ihr Anbieter für das digitale Dokumenten- & Qualitätsmanagement. ✓ Mehr erfahren
SimplerQMS helps Life Science organizations work more efficiently with their regulatory documentation through cloud-based QMS software.
Our experts accelerate regulatory process and regulatory strategy submission and innovations worldwide through customized, tech-enabled regulatory solutions.
Setting up complete quality systems or streamlining a burdensome one? Contact us for our QMS solutions for medical devices. We help you get more done, faster!
Medidee: advisory in regulatory affairs, quality insurance, clinical affairs and digital health for medical devices and in vitro diagnostics.
Home - Global Regulatory Partners, Inc.
Partner der Medizintechnik, Spezialist für Regulatory and Clinical Affairs, klinische Bewertungen und Risikomanagement.
Qualitätsmanagement Beratung und ISO 9001 Berater für klein- und mittelständische Unternehmen bundesweit. QM - Kompetent, flexibel, kostengünstig.
MEDCERT ist Spezialist für die Zertifizierung von Medizinprodukten und QM-Systemen im Medizinbereich. Als Benannte Stelle bieten wir CE-Kennzeichnung für Medizinprodukte sowie internationale Zulassungen an.
Cavendish Scott | The Standard in Quality and Environmental Consulting Since 1985.
We help MedTech startups develop their medical device from scratch. Medical Device Software and Hardware Development | Regulation for FDA, CE & NMPA.
LuminLogic is a premiere Medical Device Quality Management System used for medical device research, testing and regulatory compliance.
