Medicaldevicehq 备择方案 & 竞争对手
Templates and training courses for medical device product development and risk management. We have public and inhouse courses to choose from!
替代品和竞争对手 medicaldevicehq.com 在内容、流量和结构方面
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.
Promenade Software provides a comprehensive array of services and solutions for medical device software development and associated mobile and cloud applications. Learn more, today!
LuminLogic is a premiere Medical Device Quality Management System used for medical device research, testing and regulatory compliance.
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.
Ensure 100% medical compliance. Decomplix does your CE certification for medical devices and IVD in the pre- and post-market phase. Learn more here.
Navigating MedTech product realization has many obstacles. Having a guide with experience can help you avoid common pitfalls. Leverage our Vantage point
Proxima Clinical Research Is The Diligent FDA CRO Consultant That Works With Emerging Biotech & Medical Device Companies Across All Phases Of Development.
Our medical device development solutions include design, manufacturing, & regulatory support. We specialize in minimally invasive medical devices.
DeviceLab is a one stop shop for your medical device design, engineering, and regulation/testing. Contact us today to for a consultation!
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.
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.
Keep Calm and start creating your MDR Transition Plan - Medical Device Regulation.
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.
Oriel STAT A MATRIX has been a global leader in medical device and IVD quality and regulatory consulting, auditing and training since 1968.
The European Union Medical Device Regulation – Regulation (EU) 2017/745 (EU MDR).
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
Learn about the first and only holistic Regulatory Information Management (RIM) software for medical device companies that consolidates all the functions of regulatory affairs.
Celegence provides you with leading life sciences regulatory solutions & services for medical writing, medical device regulations, labeling, IDMP and more.
Software to manage quality management processes. From Document Control, Audits, CAPA, Supplier Vendor Management, Non Conformances & Training.
Software for Process Management, Quality Management, Complaints, CAPA, Audits and Workflow Management
Qmssystems.com is ranked number 10M in the world and links to network IP address 166.62.10.137.
A medical device quality management system (eQMS) connecting quality and regulatory compliance with a human touch. ISO 13485:2016 Certified
Medical Device consulting services - regulatory and quality - FDA, CE marking, ISO 13485, MDSAP, biological and clinical evaluation.
Located in Sterling, MA, we are an OEM medical contract manufacturing company that specializes in custom injection molded medical supplies.
Be audit-ready in every way with the best QMS software for FDA, ISO and GxP Compliance. Doc Control, Training, CAPAs, NCRs, Audits, Complaints...
Regulatory Affairs Consultancy, EU MedTech Regulation Support, EU Medical Device Regulatory affairs services, Regulatory Affairs Consultancy, Regulatory compliance for medical devices, How to ensure regulatory compliance for medical devices, Best practices for regulatory compliance in the medtech sector, Regulatory compliance software for medical devices, Regulatory compliance consulting for medical devices, CE marking for medical devices, ISO 13485 certification for medical devices, IEC 62366 compliance for medical devices, GAMP 5 training for medical devices, MDR 2017/745 compliance for medical devices, IVDR 2017/746 compliance for medical devices, Medical device risk management, Clinical trials for medical devices, Postmarket surveillance for medical devices, Product registration for medical devices, Regulatory affairs for medical devices, Quality management for medical devices, Auditing of medical devices, Training for medical device professionals, Consulting for medical device companie
SimplerQMS helps Life Science organizations work more efficiently with their regulatory documentation through cloud-based QMS software.
Lead industrial design company in New-York & Massachusetts. We work in the development of industrial design projects in the fields of medical device engineering and more.
Technosoft Innovation offers the best engineering services across the United States. Technosoft Innovation is an innovative platform for engineering services.
Omnica Corporation provides top-quality product design and engineering services for the medical device, diagnostic and other high-tech industries.
Seven out of the top ten medical device organizations chose to contract with RBC Innovations as their manufacturing company. We bring any project to life.
Promedica delivers the quality and consistent results of a large CRO with the efficiencies and responsiveness of a small CRO. Schedule a Consultation today.
IMed Consultancy Ltd provides expert guidance in quality assurance and regulatory compliance to the life science sector: IVD and Medical Device.
A full-service CRO that delivers Functional Support, Quality & Validation, Patient Recruitment and Retention, and Strategic Talent Acquisition solutions.
PROMETRIKA is a global full-service clinical research organization (CRO) with extensive experience in clinical operations, data management, biostatistics, medical writing, and pharmacovigilance.
Synteract.com is ranked number 10M in the world and links to network IP address 69.20.3.178.
Leon Research,15 years as a CRO (Contract Research Organization) and pharmaceutical consulting company in Spain, Italy and Portugal.