49:28

B2B Sales And Generating Revenue: Tatyana Eliseeva, Healthcare Startup Meetup #3

06:37

Agile Development For Medical Device Software: Is It Possible?

03:40

Launching Free Regulatory Updates: Stay Updated With The ISO 13485 And Other Standards

09:21

Jira QMS: Can You Set Up a QMS And Requirements Management In Jira For Medical Device Compliance?

05:37

Get The ISO 13485 Almost For Free: How to Buy Standards on the Estonian Website

02:18

Bringing Transparency To MDR Compliance

03:06

Free MDR Templates

08:09

ChatGPT For Medical Device Documentation (MDR / FDA)?

05:24

Software Detailed Design Documentation in Formwork

10:17

Medical Device QMS Software Comparison: Shady Business Practices!

47:35

Matthew Fenech: DiGA For Glucose Control at Una Health (Healthcare Startup Meetup #2)

05:18

MDR Clinical Evaluation: Understanding the Process

06:33

QMS Overview: Automate Your ISO 13485 Documents and Records

24:46

Leander Märkisch: Building AI For Radiology at Floy (Healthcare Startup Meetup #1)

07:04

Use ChatGPT to Generate Your QMS In Minutes

12:06

Medical Device Starter Course, Part 6: ChatGPT For Medical Devices And Automating QMS Trainings

12:48

Medical Device Starter Course, Part 5: Auto-Generate Audit Spreadsheets For Requirements Management

07:25

Medical Device Starter Course, Part 4: Saving Time By Copying OpenRegulatory Templates

04:55

Custom File Documents / Records

08:59

QMS Trainings: Automatically Train Your Employees in Formwork

07:06

Formwork Batch Export: The Only eQMS Software Without Lock-In

07:17

Manage your Technical Documentation in Formwork (eQMS software)

15:20

Medical Device Starter Course, Part 3: What next? How to save money and automate things?

14:35

Medical Device Starter Course, Part 2: What do you need to do? Looking at IEC 62304 and other docs

10:12

Medical Device Starter Course, Part 1: How much does it cost? How long does it take?

07:22

Creating a UDI For a Medical Device at IFA

09:57

Registering at GS1 To Purchase a UDI For A Medical Device

11:59

Introduction To Understanding Unique Device Identifiers (UDIs) For Medical Devices

10:16

Meet CrowdCovid (Example Medical Device Software For IEC 62304 Compliance)

05:42

Getting Started With The IEC 62366 (Usability Engineering For Software as a Medical Device)

07:34

How Does The IEC 62304 V-Model Work For Software Development Of Medical Devices?

07:07

Medical Device Software Development: Introduction To The IEC 62304

05:41

Hardware Medical Devices in Formwork

10:45

Formwork vs GitHub, Jira, ClickUp, Asana

07:56

AI-Assisted Writing of Technical Documentation

10:36

Manage Your Medical Device CAPAs in Formwork (eQMS)

09:25

Formwork: Auto-Generate Your Technical Documentation With The New Audit Export

10:46

Document and Record Control For Medical Device Quality Management Systems (ISO 13485 QMS)

06:35

Internal Audit For Medical Device Manufacturers (ISO 13485 Compliance)

11:39

Writing a Quality Manual For Medical Device Quality Management (ISO 13485)

09:06

The Magical Wizard and How It Helps You

26:01

SaMD Meetup #11: Post-Market Surveillance

13:07

Automate Your Medical Device Risk Management With Formwork, An eQMS (ISO 14971 Compliance)

06:04

Audit Export and Sanity Check

08:13

IEC 62304 - Compliant Software Requirements Specification For Software as a Medical Device (SaMD)

06:37

Employee QMS Training For ISO 13485 Compliance, Using eQMS Software

06:49

ISO 13485 - Compliant Handling Of Records, Save Time Using OpenRegulatory Templates

11:50

FDA and EU - Complaint E-Signatures: Documents and Review Workflow in eQMS Software Formwork

05:55

Introducing Formwork

01:01:58

OpenRegulatory Workshop at Digital Medicine Conference 2021

09:09

Kicky van Leeuwen: AI in Radiology, Current State of Play

11:00

Leon Doorn: Risk Management in Decision Support Systems

48:25

Pat Baird: An AI Medical Device Global Status Update (ISO, IMDRF, Legislation)

10:11

Dr. Oliver Eidel: Opening Talk

09:51

Dr. Johannes Tanne: Using git for QMS Document Control

42:31

Audience Questions and Discussion

08:54

Jouke Waleson: What's so hard about building Medical Devices for consumers?

10:40

Astrid Ottosen: Supplier Evaluation of Medical Annotators for AI SaMD

32:26

Martin Witte: Digitalization of Technical Documentation

28:15

Natascha Cuper: Common Findings in SaMD Applications and Notified Body Expectations