Digital Dentistry in Contemporary Practice From Intraoral Scanning to Integrated CAD/CAM Workflows

An introductory seminar for dental professionals who want to understand how digital data moves from patient capture and diagnosis to restorative design, manufacturing, verification and clinical delivery – and how to introduce digital workflows into practice with realistic expectations, sound quality control and appropriate clinical governance.

Delivery Format

Specialty

Program Overview

Program Overview

Digital dentistry is not a single device and it is not defined by replacing an impression tray with a scanner. It is an interconnected clinical and technical pathway in which patient information is captured, combined, interpreted, designed, manufactured, verified and retained. The quality of the final outcome depends on every transition in that pathway.

This seminar provides a structured map of the contemporary digital ecosystem. It begins with intraoral scanning and the practical conditions that influence data quality: field control, preparation visibility, tissue management, reflective surfaces, scan strategy, movement, edentulous areas, scan-body seating and the operator’s ability to identify and correct incomplete or distorted data.

Participants then follow the dataset into restorative CAD. They examine how diagnosis, preparation design, margin definition, insertion path, contacts, occlusion, anatomy and material requirements inform the virtual restoration. Chairside, laboratory and hybrid models are compared so that participants can understand where clinical control, laboratory expertise and efficient communication are most valuable.

Manufacturing is presented as more than a machine cycle. Milling, crystallisation, sintering, staining, glazing, polishing and additive manufacturing each have distinct requirements. Material selection is connected to indication, restoration design, thickness, strength, aesthetics, bonding or cementation and the manufacturer’s current instructions.

The seminar also introduces more complex digital applications: implant scanning, full-arch records, integration of surface data with justified CBCT, guided surgery, digital wax-ups, facial data, smile planning, occlusal appliances and 3D printing. These topics are taught with their limitations and verification requirements. The presence of a technology in a workflow does not guarantee accuracy, passive fit, safety or a predictable clinical result.

Finally, participants explore how to decide whether and how to adopt a digital workflow. The discussion includes staff roles, training, laboratory collaboration, service and subscriptions, file compatibility, data security, maintenance, downtime, remakes, time-per-case and the distinction between a compelling demonstration and a sustainable clinical system.

Entry Requirements

Appropriate dental or dental-technology qualification for the participant's role

Lawful professional scope for any clinical application discussed or later undertaken

Basic understanding of indirect restorative dentistry and clinical record keeping

No previous CAD/CAM ownership or software experience is required for the introductory seminar unless stated for a specific edition

Any participant-provided case must be de-identified and submitted only through the secure pathway announced by the organiser

No identifiable photographs, radiographs, DICOM files, surface scans or laboratory prescriptions should be uploaded through a general registration form

Participants using a demonstration workstation must follow the edition-specific data, equipment and infection-control instructions

Those seeking competence in CBCT, guided surgery, manufacturing or specific clinical procedures will require additional training beyond this seminar

Highlights

Program Highlights

The complete digital pathway: capture, evaluate, design, manufacture, finish, verify and document

Intraoral scanning principles, scan strategy and quality-control checkpoints

Digital impressions for teeth, implants and selected arch indications

Accuracy, trueness, precision and the clinical meaning of digital error

Chairside, laboratory and hybrid CAD/CAM workflows

Restorative design from single units to more complex indications

Material selection according to indication, design and processing pathway

Subtractive manufacturing: milling, tool access, nesting and post-processing

Staining, glazing, crystallisation, sintering and polishing as distinct procedures

Implant scan bodies, data capture and verification of multi-unit or full-arch records

Digital wax-ups, smile planning, facial data and the virtual patient concept

Integration of CBCT and surface scans for implant planning

Guided implant surgery workflow, cumulative error and safety boundaries

Digital design and 3D printing of occlusal appliances and other approved applications

Practice-laboratory communication, file exchange and traceability

Workflow timing, true cost, return-on-investment assumptions and implementation planning

Data protection, consent, cybersecurity and responsible use of patient files

Demonstrations and case-based discussion according to the announced edition

Learning Objectives

What You Will Learn

  • Map the principal stages of an integrated digital dental workflow.
  • Identify common types of digital clinical data and explain their different purposes and limitations.
  • Describe the factors that influence intraoral scan quality and recognise common scanning defects.
  • Distinguish suitable applications for straightforward tooth-supported scanning from more demanding complete-arch and implant workflows.
  • Explain the importance of scan-body compatibility, seating, visibility, library selection and verification.
  • Describe the principal CAD steps for a basic indirect restoration and the clinical decisions that remain operator-dependent.
  • Compare chairside, laboratory and hybrid workflows at a conceptual level.
  • Relate restorative material selection to indication, design, processing and current instructions for use.
  • Distinguish milling, crystallisation, sintering, staining, glazing and polishing.
  • Explain the principal stages and quality-control requirements of an additive manufacturing workflow.
  • Describe how intraoral, facial and imaging datasets may contribute to a virtual patient while recognising registration error.
  • Explain why digital smile simulations support communication but do not guarantee treatment outcomes.
  • Outline the workflow for computer-guided implant planning and identify major sources of cumulative error.
  • Explain why CBCT requires individual justification, optimisation and complete-dataset evaluation.
  • Recognise why full-arch implant records require additional verification before a definitive prosthesis is produced.
  • Build a preliminary implementation checklist including training, people, equipment, laboratory, data, costs and backup planning.
  • Ask more informed questions before investing in or expanding a digital system.
  • Define the limits of an introductory seminar and identify the product-specific or clinical training needed next.
Content

Program Content

01

Module 1 - Building the Digital Patient

  • What makes a workflow digital and where clinical responsibility remains
  • Intraoral scans, photographs, radiographs, CBCT, facial scans and jaw records
  • Open and proprietary file ecosystems: STL, PLY, OBJ and DICOM concepts
  • Dataset quality, alignment and registration error
  • Consent, de-identification, access, storage and secure transfer
02

Module 2 - Predictable Intraoral Scanning

  • Scanner principles and indication-specific expectations
  • Field preparation, moisture, tissue displacement and margin visibility
  • Scan strategy, landmarks, bite records and rescanning
  • Detecting holes, stitching errors, artefacts and distorted data
  • Tooth-supported, edentulous and implant-supported differences
  • Final scan approval before design or laboratory transfer
03

Module 3 - Restorative CAD and Material Decisions

  • Case setup, restoration type and margin confirmation
  • Insertion path, spacer, contacts, occlusion and morphology
  • Automated proposals and the need for operator review
  • Minimum dimensions and material-specific design limits
  • Glass ceramics, zirconia, polymers, composites and other announced materials
  • Chairside, laboratory and hybrid workflow selection
04

Module 4 - Manufacturing and Finishing

  • Block/disc selection, nesting, bur access and milling strategy
  • Wet and dry processing, machine care and calibration awareness
  • Crystallisation versus sintering
  • Staining, glazing and polishing as separate finishing routes
  • Additive manufacturing: design, orientation, supports, washing and post-curing
  • Traceability, inspection and acceptance criteria before clinical delivery
05

Module 5 - Implant and Full-Arch Digital Workflows

  • Scan bodies, component libraries and seating verification
  • Scan span, landmarks, soft tissue and cumulative error
  • Single implant versus multi-unit and complete-arch records
  • Passive fit as a verified objective, not a scanner promise
  • Verification jigs, photogrammetry and alternative validation concepts
  • When to rescan, repeat, supplement or refer
06

Module 6 - CBCT Integration and Guided Surgery

  • Restoratively driven planning and the clinical question
  • Justified CBCT, field of view, image quality and full-volume evaluation
  • Surface scan and DICOM registration
  • Virtual implant position, anatomy and safety margins
  • Guide design, support, sleeves, manufacture and verification
  • Cumulative deviation and intraoperative control
07

Module 7 - Smile Design, Virtual Patient and 3D Applications

  • Standardised photographs, video and facial references
  • Digital wax-up and treatment communication
  • Smile simulation versus clinical feasibility
  • Combining facial, intraoral and imaging data
  • Digital design of occlusal appliances
  • 3D-printed models, guides, provisionals and other approved indications
08

Module 8 - Practice Integration and Business Planning

  • Selecting an appropriate first workflow
  • Training, team roles and standard operating procedures
  • Laboratory communication and file-acceptance protocols
  • Equipment, software, service, subscriptions and interoperability
  • Time-per-case, remakes, downtime and complete cost calculation
  • Pilot cases, key performance indicators and staged adoption
09

Demonstration and Case Discussion

  • Live or recorded scan, design, manufacture or finishing demonstration as announced
  • Guided review of complete and defective datasets
  • Case-based comparison of chairside, laboratory and hybrid options
  • Discussion of implant, smile-design and 3D-printing workflows
  • Questions focused on indications, limitations, verification and implementation
  • Exact systems, software versions and participant access confirmed for each edition
Description

Detailed Program Description

The seminar opens by defining a digital workflow and identifying the information that may form the digital patient record: intraoral surface scans, photographs, radiographs, CBCT when justified, facial scans, jaw-relation records and existing clinical documentation. Participants learn that datasets have different purposes, resolutions, sources of error and responsibilities, and that their successful alignment does not prove diagnostic validity.

The intraoral scanning section follows a preparation or arch from initial field assessment to final data approval. It addresses moisture and soft-tissue control, margin exposure, scan path, bite capture, interproximal and occlusal data, deletion and rescanning, artefact recognition and the difference between an attractive colour model and a clinically adequate digital impression. Tooth-supported and implant-supported records are distinguished, including the importance of compatible scan bodies, complete seating, cleanliness, visibility, library selection and verification.

Restorative CAD is introduced through a stepwise design sequence. Participants review case setup, restoration type, margin confirmation, insertion axis, spacer parameters, proximal contacts, dynamic and static occlusion, morphology and minimum material dimensions. The seminar explains why automated proposals are starting points rather than final clinical decisions and why design must remain connected to preparation quality, biology, function, cleansability and the selected manufacturing material.

The manufacturing section compares subtractive and additive methods. For milling, it examines block or disc selection, bur geometry, tool access, nesting, machine maintenance and the distinction between wet and dry processing. Post-milling steps – crystallisation, sintering, staining, glazing and polishing – are separated and connected to their specific materials. For 3D printing, the seminar introduces validated resins, orientation, supports, layer parameters, washing, post-curing, finishing, environmental controls, traceability and final inspection.

Complex restorative and implant workflows are then placed on a risk continuum. Participants see why the accuracy requirements and error propagation of a single crown differ from those of a long-span restoration or complete-arch implant framework. The concepts of stitching error, scan-body geometry and distribution, soft-tissue mobility, lack of landmarks, verification jigs, photogrammetry and clinical fit assessment are introduced without promoting a single universal capture method.

For implant planning, the seminar maps the path from clinical and prosthetic objectives to imaging, surface scanning, dataset registration, virtual implant positioning, guide design, support, sleeve and drill considerations, manufacturing and intraoperative verification. It emphasises that each step can add error. CBCT is included only when justified, with attention to the smallest suitable field of view, appropriate exposure, quality assurance and evaluation of the entire volume.

The digital smile and virtual patient section explains how photographs, video, facial scans, intraoral scans and virtual wax-ups can support analysis, communication and provisionalisation. Participants consider calibration, head position, lip dynamics, facial references, occlusion, periodontal and restorative constraints, and the need to communicate that a simulation is not a guaranteed preview of the final result.

The final section turns the clinical map into an adoption plan. Participants identify suitable first indications, required training, staff responsibilities, laboratory interfaces, backup procedures and measurable outcomes. A complete cost model is introduced, including finance, software, service, consumables, staff time, maintenance, calibration, remakes, storage and downtime. The goal is to support a staged, evidence-aware decision rather than technology adoption based solely on speed or marketing appeal.

Certification

Trainer and Certification

The seminar combines structured teaching, workflow mapping, visual demonstration, case-based discussion and guided evaluation of digital records. Depending on the edition, a live system may be used to demonstrate scanning, restorative design, milling, furnace processing or another selected part of the workflow. The exact duration, language, class size, platform, software version, materials, equipment, participant access and practical format are announced separately. A demonstration does not mean that every participant will operate the system or produce a restoration. Individual hands-on training should be stated only when sufficient workstations, supervision, time and materials have been confirmed. Any certificate of attendance or completion, assessment and CPD/CME recognition will be stated only when formally confirmed. Attendance does not authorise a participant to interpret CBCT, perform guided implant surgery, manufacture regulated devices or independently use unfamiliar equipment. Product instructions, applicable law, clinical governance and further supervised training remain essential.
Who is the Program For

Who Should Attend

This seminar is intended primarily for qualified dentists who want a structured introduction to digital clinical and restorative workflows, are considering their first digital investment, already own an intraoral scanner or CAD/CAM system but use only part of its capabilities, or want to improve communication with a digital dental laboratory.

Dental technicians and appropriately trained members of a digital dental team may also benefit where the edition is opened to them. The seminar is introductory and strategic. It is not a substitute for product-specific operator training, formal CBCT training, implant-surgery education, laboratory technician training or supervised clinical competency development.

Frequently Asked Questions

FAQs

Yes. It provides a structured introduction to the ecosystem and helps participants understand where to begin. It is not a substitute for hands-on operator training on a selected system.

No. The permanent program is vendor-neutral. A particular edition may use a named system for demonstration, and that platform will be stated before registration.

You will learn the principles, quality checkpoints, common errors and workflow logic. Individual operating time is included only if the event listing expressly confirms hands-on scanning.

No. Suitability depends on the indication, anatomy, field control, span, restorative objective, equipment and validated workflow. Complete-arch and implant cases require particular caution and verification.

No. Passive fit is a clinical and technical objective that must be verified. Scan-body seating, scan strategy, span, data processing, manufacturing and clinical assessment can all affect fit.

No. It explains CBCT's role in selected digital workflows and the principles of justification, optimisation and data integration. Formal interpretation and operator competence require appropriate additional training and legal compliance.

No. The seminar introduces the workflow, indications, sources of error and safety boundaries. Guided surgery requires implant training, product-specific education, planning competence and appropriate supervised clinical development.

No. They are communication and planning aids. Biological, periodontal, functional, restorative and patient-related factors may alter what is clinically achievable.

It introduces the digital design-to-print workflow and its quality controls. A live print, individual design exercise or printed take-home item is included only when specifically announced.

A live or recorded example may be shown depending on the edition. The material, restoration, machine, furnace and final outcome will be stated separately and are not permanent inclusions.

It provides a framework for matching technology to clinical need and calculating training, staff time, subscriptions, service, consumables, maintenance, remakes, laboratory costs and downtime. It does not promise a guaranteed return.

Only if these are expressly confirmed for the specific edition. Attendance alone is not certification of clinical or technical competence.
Program Training & Certification

Training & Certification

The seminar combines structured teaching, workflow mapping, visual demonstration, case-based discussion and guided evaluation of digital records. Depending on the edition, a live system may be used to demonstrate scanning, restorative design, milling, furnace processing or another selected part of the workflow. The exact duration, language, class size, platform, software version, materials, equipment, participant access and practical format are announced separately. A demonstration does not mean that every participant will operate the system or produce a restoration. Individual hands-on training should be stated only when sufficient workstations, supervision, time and materials have been confirmed. Any certificate of attendance or completion, assessment and CPD/CME recognition will be stated only when formally confirmed. Attendance does not authorise a participant to interpret CBCT, perform guided implant surgery, manufacture regulated devices or independently use unfamiliar equipment. Product instructions, applicable law, clinical governance and further supervised training remain essential.
Enquire Now

Interested In This Program

    Stay Connected

    See the complete digital workflow before choosing your next digital step.

    Understand how data moves from scan to design, manufacture and clinical verification - and learn where digital technology adds value, where error can enter and what a sustainable implementation plan requires.
    This site is registered on wpml.org as a development site. Switch to a production site key to remove this banner.