Promenadesoftware 备择方案 & 竞争对手
Promenade Software provides a comprehensive array of services and solutions for medical device software development and associated mobile and cloud applications. Learn more, today!
替代品和竞争对手 promenadesoftware.com 在内容、流量和结构方面
Templates and training courses for medical device product development and risk management. We have public and inhouse courses to choose from!
Team-NB is the European Association of Notified Bodies active in the Medical device sector. The members are Notified Bodies under any or all of the three medical device directives: 90/385/EEC; 93/42/EEC; 98/79/EC.
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.
Navigating MedTech product realization has many obstacles. Having a guide with experience can help you avoid common pitfalls. Leverage our Vantage point
OpenRegulatory: Learn How to Certify Software as a Medical Device.
Providing product development for medical devices, life sciences, & consumer health in San Diego and worldwide. Shaping innovation in medical design.
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.
OWASP CycloneDX is a full-stack Bill of Materials (BOM) standard that provides advanced supply chain capabilities for cyber risk reduction. The specification supports Software Bill of Materials (SBOM), Software-as-a-Service Bill of Materials (SaaSBOM), Hardware Bill of Materials (HBOM), Operations Bill of Materials (OBOM), Vulnerability Disclosure Reports (VDR), and Vulnerability Exploitability eXchange (VEX).
Adolus.com is ranked number 10M in the world and links to network IP address 76.76.21.21.
Unioncrate.com réunit des informations et annonces. Nous espérons que vous y trouverez les informations que vous recherchez !
Oriel STAT A MATRIX has been a global leader in medical device and IVD quality and regulatory consulting, auditing and training since 1968.
The leading MedTech Services provider, offering Medical Device Consulting, clinical trial, lab & reimbursement services to support the entire product lifecycle.
I3cglobal.com is ranked number 10M in the world.
Keep Calm and start creating your MDR Transition Plan - Medical Device Regulation.
The European Union Medical Device Regulation – Regulation (EU) 2017/745 (EU MDR).
Be audit-ready in every way with the best QMS software for FDA, ISO and GxP Compliance. Doc Control, Training, CAPAs, NCRs, Audits, Complaints...
Located in Sterling, MA, we are an OEM medical contract manufacturing company that specializes in custom injection molded medical supplies.
SimplerQMS helps Life Science organizations work more efficiently with their regulatory documentation through cloud-based QMS software.
Proxima Clinical Research Is The Diligent FDA CRO Consultant That Works With Emerging Biotech & Medical Device Companies Across All Phases Of Development.
DeviceLab is a one stop shop for your medical device design, engineering, and regulation/testing. Contact us today to for a consultation!
Our medical device development solutions include design, manufacturing, & regulatory support. We specialize in minimally invasive medical devices.
LuminLogic is a premiere Medical Device Quality Management System used for medical device research, testing and regulatory compliance.
Ensure 100% medical compliance. Decomplix does your CE certification for medical devices and IVD in the pre- and post-market phase. Learn more here.
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!
We help MedTech startups develop their medical device from scratch. Medical Device Software and Hardware Development | Regulation for FDA, CE & NMPA.
Dependency-Track is a continuous SBOM analysis platform that allows organizations to identify and reduce risk in the software supply chain. Dependency-Track is open-source and distributed under the Apache 2.0 license.
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We make licensing easy for humans and machines alike. REUSE solves a fundamental issue that Free Software licensing has at the very source. Adopting our recommendations is as easy as one-two-three!
The Distribution Solution (TDS) offers storage fulfilment and distribution services plus fulfilment warehousing for retailers and online e-commerce stores in UK and Ireland. We also ship and distribute to Europe.
Our one-of-a-kind, enterprise solution empowers brands to efficiently convert slow-moving and excess inventory into working capital.
Der Regulatory Affairs Blog für alle Themen rund um die internationale Zulassung von medizintechnischen Produkten.
A simple, free, indented bill of materials tool using an open source project. Integrated with modern tools like Octopart to pull in the latest sourcing information to optimize your BOM for cost, and Google Drive for quick access to your files (coming soon). Get rid of your PLM tool and try IndaBOM!
Demand planning, forecasting and optimization software for your business. Prevent stockouts, reduce excess stock, and maximize your inventory ROI with our AI.
It’s time to put strength back in your supply chain planning. Transform your supply chain into an AI-driven digital platform with John Galt Solutions.
Learn about the first and only holistic Regulatory Information Management (RIM) software for medical device companies that consolidates all the functions of regulatory affairs.
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
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.