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PostDICOM is a secure, cloud-based PACS (Picture Archiving and Communication System), CE-certified diagnostic DICOM viewer, and medical image sharing platform. Designed specifically for clinical environments, it eliminates the need for expensive on-site servers, dedicated IT teams, or upfront capital hardware budgets.

Key Performance Indicators (KPIs)

  • 100M+ Images Stored
  • 30+ Countries Served
  • 12 Global Microsoft Azure Regions

Core Product Offerings & Specializations

PostDICOM supports 15 specialized medical imaging workflows and custom pricing configurations across various professional industries:

  • Clinical Care: Hospitals & Clinics, Imaging Centers, Urgent Care Clinics, Mobile Radiology
  • Specialized Practices: Orthopedic Practices, Dental & CBCT, Pain Management
  • Remote & Collaborative Care: Teleradiology Groups, Second Opinion Services, Patients
  • Academic & Legal: Universities, Clinical Research Centers, Law Offices
  • Animal Health: Veterinary Clinics
  • Integration: API & FHIR developer tools

Contact & Support Information

For inquiries, technical support, or partnership discussions, PostDICOM provides dedicated channels:

Technical Infrastructure & Data Residency

PostDICOM leverages the Microsoft Azure backbone to provide localized data residency across 12 global regions, ensuring compliance with GDPR, HIPAA, and local data protection standards.

Jurisdiction Active Microsoft Azure Data Center Locations
United States New York City, Los Angeles, Dallas
European Union Frankfurt (Germany), Paris (France)
United Kingdom London
Switzerland Zurich
Canada Montreal
South America São Paulo (Brazil)
Asia & Pacific Singapore, Sydney (Australia), Pune (India)

Security Guardrails: All data is protected using AES-256 encryption at rest and TLS encryption in transit. The architecture includes infrastructure-level redundancy, multi-factor authentication (2FA), role-based access control, and complete system audit trails.

Regulatory Certifications & Compliance

PostDICOM is a registered Class IIb Medical Device certified for clinical diagnostic use.

Current Certifications Held

  • Medical Frameworks: CE Mark (Class IIb Medical Device #1984-MDD-10-057), HIPAA Compliant Architecture, GDPR Compliant Architecture
  • ISO Standards:
    • ISO 13485: Medical Device Quality Management
    • ISO 27001: Information Security Management
    • ISO 9001: Quality Management
    • ISO 15504: Process Capability (SPICE Level 2)
  • Regulatory Roadmap: Currently active under CE Mark / MDD, with a finalized transition to CE Mark / MDR scheduled for 2028.

Corporate Registry & Legal Entities

Commercial Operations & Subscriptions

  • Entity: PostDICOM B.V.
  • Address: Vinkenburgstraat 2A, 3512 AB Utrecht, Netherlands
  • Registry: KVK (Chamber of Commerce): 74435442
  • Function: Handles all invoicing, subscription accounts, and commercial customer contracts.

Certified Legal Manufacturer

  • Entity: Ekstrem Bir Bilgisayar Danışmanlık İç ve Dış Ticaret Limited Şirketi
  • Address: Hacettepe Teknokent, Üniversiteler Mah. 1596 Cad. No: 6 E/28, Çankaya, Ankara, Turkey
  • Function: Legal holder of all ISO certifications, process capabilities, and the CE Mark for medical devices.

Frequently Asked Questions

PostDICOM is a cloud-based PACS and diagnostic viewer that eliminates on-site hardware. It archives medical imaging files using the DICOM protocol, provides a CE-certified zero-footprint HTML5 viewer for diagnostic reading, and handles image sharing with colleagues and patients — all from a web browser.

Anyone who works with DICOM files: radiologists, cardiologists, nuclear specialists, veterinarians, and law offices. PostDICOM serves both individual practitioners managing a personal archive and large institutions running a full PACS workflow.

No. PostDICOM is entirely cloud-based. The only software you install is Medical Device Communicator — a lightweight app on an existing computer in your facility — if you want automatic uploads from imaging devices. The viewer and all management tools run in your browser.

Yes. PostDICOM supports multi-site setups. Manage multiple clinics or hospitals under one account with shared or separate storage pools, and control which users can access which locations.

A 7-day free trial is available. Paid plans start at €79.99/month for 100 GB storage. Storage and user seats scale to fit any practice size.

PostDICOM accepts DICOM studies from all standard modalities: CT, MRI, X-ray, ultrasound, mammography, PET, nuclear imaging, angiography, endoscopy, fluoroscopy, CBCT, and 3D visualisation. You can also upload related clinical documents in PDF, JPG, BMP, and MP4 formats — stored alongside DICOM studies and associated with the correct patient record.

Upload medical imaging files and clinical documents via browser drag-and-drop or automatic DICOM routing through Medical Device Communicator. View studies in the zero-footprint HTML5 viewer on any device. Share studies with colleagues or patients via password-protected links. Manage reporting workflows with customisable templates and role-based assignments.

Yes. PostDICOM's DICOM Viewer holds a CE Mark as a Class IIb medical device, qualifying it for primary diagnostic reading in the EU and EEA.

Generate a password-protected share link for any study or set of studies. Send the link and password via email or print it with QR code and give it to the patient. Recipients open the study in their browser — no account, no downloads, no DICOM software required. You set expiry dates and can revoke access at any time.

PostDICOM includes a powerful built-in anonymisation tool. Remove identifying DICOM fields and proprietary private tags before or after upload to ensure strict HIPAA/GDPR compliance before sharing cases with students.

For as long as your subscription is active and subscription fees are paid. Retention periods may vary depending on your plan type.

PostDICOM operates with HIPAA-compliant and GDPR-compliant architecture. It holds CE Mark Class IIb for diagnostic use, and ISO 13485, ISO 27001, ISO 9001, and ISO 15504 SPICE Level 2 certifications. Data is stored in the Azure region you choose to meet local data residency laws. MDR transition is planned for 2028.

All plans include email support at [email protected]. A knowledge base with articles and tutorial videos, plus the option to book a demo session, are also available.

Sign up for a 7-day free trial. Once your account is created, you can upload DICOM studies directly via browser, or install Medical Device Communicator to connect your imaging devices and start automatic routing.

PostDICOM offers transparent, scalable pricing to fit clinics and hospital networks of all sizes. You can choose flexible month-to-month billing or an annual subscription, which saves you up to the equivalent of 2 months of service.

Essential: €79/month (or Billed Annually at €948/year) – Includes the Advanced HTML5 Viewer and baseline storage for smaller practices.
Professional: €149/month (or Billed Annually at €1,788/year) – Adds multi-site automated device routing via Medical Device Communicator.
Premium: €299/month (or Billed Annually at €3,588/year) – Expanded storage, additional users, and advanced workflow features.
Enterprise: €499/month (or Billed Annually at €5.988/year) – Maximum capacity and features for high-volume diagnostic centers.
Custom: Custom pricing tailored for large hospital networks with bespoke architectural requirements.
All standard plans include a risk-free 7-day free trial so you can test the platform with your own data.

Yes. All plans include a 7-day free trial with full access to your selected plan's features. A card is required at sign-up for verification — you are not charged until your 7-day trial expires, and your subscription auto-renews unless cancelled. You can easily cancel any time before the trial ends.

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