Greenlight البدائل & المنافسين
Greenlight Guru brings modern QMS and EDC software to 1,000+ medical device companies helping improve speed and efficiency while reducing risk.
البدائل والمنافسين ل greenlight.guru من حيث المحتوى وحركة المرور والهيكل
Medical Device and Diagnostic Industry (MD+DI) is the primary resource for manufacturers of medical devices and in vitro diagnostic products.
Be audit-ready in every way with the best QMS software for FDA, ISO and GxP Compliance. Doc Control, Training, CAPAs, NCRs, Audits, Complaints...
Are you a start-up device company that needs medical device consulting services and training for an FDA 510k submission?
MasterControl’s modern MES and QMS ensure compliance with regulations, reduce risks, and improve the quality and safety of products for regulated industries like Life Sciences.
Emergo: medical device consultants for QA/RA, device registration, clinical trials, reimbursement and distribution consulting. Offices worldwide.
A comprehensive listing of companies, products and services for medical device manufacturers.
Medical Design & Outsourcing covers technical advancements fueling innovation in medical device design, development and manufacturing.
Home - Medical Device Network.
The Medical Device Business Journal — Medical Device News & Articles | MassDevice
SimplerQMS helps Life Science organizations work more efficiently with their regulatory documentation through cloud-based QMS software.
Navigating MedTech product realization has many obstacles. Having a guide with experience can help you avoid common pitfalls. Leverage our Vantage point
ComplianceQuest is a highly flexible 100% cloud based EQMS, quality management system and Quality Management Software built upon Salesforce platform to streamline quality, compliance, content and collaboration management workflows.
Qualityze offers the perfect blend of cutting-edge Quality Management Software for all your business challenges! Choose Us, Choose Success!
Oriel STAT A MATRIX has been a global leader in medical device and IVD quality and regulatory consulting, auditing and training since 1968.
Lne-america.com is ranked number 1985982 in the world and links to network IP address 205.134.253.67.
Emergo: medical device consultants for QA/RA, device registration, clinical trials, reimbursement and distribution consulting. Offices worldwide.
Montrium is a leading electronic content management solution provider for life science organizations.
Homepage | ISPE | International Society for Pharmaceutical Engineering.
Stay in control with the most complete enterprise quality management system, SmartSolve®. Prepare to succeed with Pilgrim's EQMS software.
The world's only 100% medical device-focused, full development Contract Research Organization (CRO). Learn how to accelerate your development program today!
World leading Wellkang Tech Consulting group help you in (CE Marking) CE Mark (EC Mark) approval, ce testing for Medical Devices (MDD), Personal Protective Equipment (PPE), Low Voltage Electrical Equipment (LVD), Electromagnetic Compatibility (EMC), Machinery, Toys, etc
MedTech Dive provides medical technology news and analysis for industry professionals. We cover medical devices, diagnostics, digital health, FDA regulation and compliance, imaging, and more.
Biopharma is a fast-growing world where big ideas come along daily. Our subscribers rely on Fierce Biotech as their must-read source for the latest news, analysis and data in the world of biotech and pharma R&D.
Discover Scilife, a smart quality management software for Life Sciences, to digitize quality processes, boost performance, and become fully compliant!
The AssurX platform is an automated Quality Management System Software used to improve quality, compliance and better manage any enterprise.
Cognidox is a document management system that helps streamline complex product development cycles. As a lean DMS, we support quality and lean processes.
Rocky Mountain Regulatory Affairs Society, Centennial
IsoTracker's modular QMS software makes document control, complaint and audit management and non-conformance management quicker and easier.
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.
Regulatory and Quality Solutions (R&Q) provides industry-leading regulatory and quality consulting and engineering services to medical device and combination product companies.
Located in Sterling, MA, we are an OEM medical contract manufacturing company that specializes in custom injection molded medical supplies.
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.
TrackWise Digital is a first-of-its-kind AI-powered QMS platform to help you be ready for what’s next.
Mdc medical device certification GmbH - Startseite.
Verse Solutions provides Total Quality Management (TQM) Software that enables manufacturers of all sizes to mitigate compliance management. Features/modules include: Document Control, Employee Training, Corrective Action, Audit Management, Risk Register and Centralizes Reporting.
Ce-marking.com is ranked number 10M in the world and links to network IP address 50.63.197.205.
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.
Welcome to the City of Brampton.
Intelex cloud based software manages Environment, Health & Safety, ESG, Quality and Suppliers for regulatory compliance, and streamline ISO initiatives.
MaintainX helps you track your reactive maintenance, preventive maintenance, and control the daily operations of your business. Get started for Free!
The FDA Group is a leader in life science consulting, staff augmentation, remediation support, auditing, and other quality system services.
Ofni Systems - Software, consulting and compliance training on 21 CFR Part 11, Electronics Records and Electronic Signatures for FDA-regulated companies.