Greenlight Guru subject lines
87 subject lines averaging 63 characters.
| Picture | Sent (Eastern) | Subject | Characters | Preview text | |
|---|---|---|---|---|---|
| Jul 2, 2026 10:01 AM | Greenlight Guru achieves ISO 42001 AI governance certification | 62 | Greenlight Guru achieves ISO 42001 AI governance certification 96 As the first medtech QMS… | Jul 2, 2026 10:01 AM · 62 characters. Greenlight Guru achieves ISO 42001 AI governance certification 96 As the first medtech QMS… | |
| Jun 30, 2026 11:19 AM | Webinar: AI in practice: how clinical investigation teams are working smarter right now | 88 | Webinar: AI in practice: how clinical investigation teams are working smarter right now 96… | Jun 30, 2026 11:19 AM · 88 characters. Webinar: AI in practice: how clinical investigation teams are working smarter right now 96… | |
| Jun 29, 2026 11:21 AM | How is AI changing clinical investigations? | 43 | How is AI changing clinical investigations? 96 The answer, and much more, in this week's… | Jun 29, 2026 11:21 AM · 43 characters. How is AI changing clinical investigations? 96 The answer, and much more, in this week's… | |
| Jun 24, 2026 10:19 AM | Whitepaper: SaMD quality ops: why Jira and GitHub belong inside your QMS | 73 | Whitepaper: SaMD quality ops: why Jira and GitHub belong inside your QMS 96 SaMD teams… | Jun 24, 2026 10:19 AM · 73 characters. Whitepaper: SaMD quality ops: why Jira and GitHub belong inside your QMS 96 SaMD teams… | |
| Jun 23, 2026 12:14 PM | Webinar: How to avoid seeing your name published in an FDA warning letter | 74 | Webinar: How to avoid seeing your name published in an FDA warning letter 96 June 25 is… | Jun 23, 2026 12:14 PM · 74 characters. Webinar: How to avoid seeing your name published in an FDA warning letter 96 June 25 is… | |
| Jun 22, 2026 11:14 AM | eBook: Your guide to clinical evaluation of a medical device | 60 | eBook: Your guide to clinical evaluation of a medical device 96 Clinical evaluation is… | Jun 22, 2026 11:14 AM · 60 characters. eBook: Your guide to clinical evaluation of a medical device 96 Clinical evaluation is… | |
| Jun 19, 2026 7:51 AM | Webinar: How to avoid seeing your name published in an FDA warning letter | 74 | Webinar: How to avoid seeing your name published in an FDA warning letter 96 FDA issued… | Jun 19, 2026 7:51 AM · 74 characters. Webinar: How to avoid seeing your name published in an FDA warning letter 96 FDA issued… | |
| Jun 17, 2026 10:15 AM | Join us tomorrow: closing the loop on post-market data | 54 | Join us tomorrow: closing the loop on post-market data 96 The session is tomorrow. If… | Jun 17, 2026 10:15 AM · 54 characters. Join us tomorrow: closing the loop on post-market data 96 The session is tomorrow. If… | |
| Jun 15, 2026 10:18 AM | How can you use AI to turn post-market data into better designs? | 64 | How can you use AI to turn post-market data into better designs? 96 The answer, and much… | Jun 15, 2026 10:18 AM · 64 characters. How can you use AI to turn post-market data into better designs? 96 The answer, and much… | |
| Jun 10, 2026 8:20 AM | Webinar: Closing the loop, using AI to turn post-market data into better designs | 81 | Webinar: Closing the loop, using AI to turn post-market data into better designs 96 Join… | Jun 10, 2026 8:20 AM · 81 characters. Webinar: Closing the loop, using AI to turn post-market data into better designs 96 Join… | |
| Jun 9, 2026 10:33 AM | eBook: Best QMS software comparison | 35 | eBook: Best QMS software comparison 96 Your guide to the different QMS software options… | Jun 9, 2026 10:33 AM · 35 characters. eBook: Best QMS software comparison 96 Your guide to the different QMS software options… | |
| Jun 5, 2026 7:53 AM | Whitepaper: AI, PCCP, and the FDA requirements that will catch SaMD teams off guard | 84 | Whitepaper: AI, PCCP, and the FDA requirements that will catch SaMD teams off guard 96… | Jun 5, 2026 7:53 AM · 84 characters. Whitepaper: AI, PCCP, and the FDA requirements that will catch SaMD teams off guard 96… | |
| Jun 4, 2026 4:49 AM | Last chance: Rethinking change control for software medical devices in Europe | 78 | Last chance: Rethinking change control for software medical devices in Europe 96 Today's… | Jun 4, 2026 4:49 AM · 78 characters. Last chance: Rethinking change control for software medical devices in Europe 96 Today's… | |
| Jun 2, 2026 1:20 PM | Webinar: Rethinking change control for software medical devices in Europe | 74 | Webinar: Rethinking change control for software medical devices in Europe 96 The EU MDR… | Jun 2, 2026 1:20 PM · 74 characters. Webinar: Rethinking change control for software medical devices in Europe 96 The EU MDR… | |
| Jun 1, 2026 10:49 AM | How do notified bodies handle changes to SaMD? | 46 | How do notified bodies handle changes to SaMD? 96 The answer, and much more, in this… | Jun 1, 2026 10:49 AM · 46 characters. How do notified bodies handle changes to SaMD? 96 The answer, and much more, in this… | |
| May 27, 2026 10:18 AM | What auditors are actually finding after QMSR took effect | 57 | What auditors are actually finding after QMSR took effect 96 The QMSR is in effect. Here's… | May 27, 2026 10:18 AM · 57 characters. What auditors are actually finding after QMSR took effect 96 The QMSR is in effect. Here's… | |
| May 25, 2026 10:38 AM | Whitepaper: FDA and CMS are rewriting the rules on device access | 64 | Whitepaper: FDA and CMS are rewriting the rules on device access 96 Here's what medtech… | May 25, 2026 10:38 AM · 64 characters. Whitepaper: FDA and CMS are rewriting the rules on device access 96 Here's what medtech… | |
| May 21, 2026 11:33 AM | Webinar: Handling audits around the QSR to QMSR transition | 58 | Webinar: Handling audits around the QSR to QMSR transition 96 QMSR is here. Auditors are… | May 21, 2026 11:33 AM · 58 characters. Webinar: Handling audits around the QSR to QMSR transition 96 QMSR is here. Auditors are… | |
| May 19, 2026 11:23 AM | 2 days out: See AI built for medtech in action | 46 | days out: See AI built for medtech in action 96 Live Thursday: Troy Michels and Will… | May 19, 2026 11:23 AM · 46 characters. days out: See AI built for medtech in action 96 Live Thursday: Troy Michels and Will… | |
| May 18, 2026 10:03 AM | How does AI really fit into medtech? | 36 | How does AI really fit into medtech? 96 Find out what intentional AI looks like in an eQMS | May 18, 2026 10:03 AM · 36 characters. How does AI really fit into medtech? 96 Find out what intentional AI looks like in an eQMS | |
| May 14, 2026 10:16 AM | Webinar: AI built for medtech. Here's what that looks like. | 59 | Webinar: AI built for medtech. Here's what that looks like. 96 Your best people shouldn't… | May 14, 2026 10:16 AM · 59 characters. Webinar: AI built for medtech. Here's what that looks like. 96 Your best people shouldn't… | |
| May 12, 2026 12:12 PM | Still time to register: How to work with a medtech CRO and stay in control | 75 | Still time to register: How to work with a medtech CRO and stay in control 96 The webinar… | May 12, 2026 12:12 PM · 75 characters. Still time to register: How to work with a medtech CRO and stay in control 96 The webinar… | |
| May 11, 2026 10:46 AM | eBook: What comes after launch? | 31 | eBook: What comes after launch? 96 A practical guide to the stages of post-market maturity… | May 11, 2026 10:46 AM · 31 characters. eBook: What comes after launch? 96 A practical guide to the stages of post-market maturity… | |
| May 7, 2026 8:51 PM | Tomorrow: see how Ultralight works for software teams | 53 | Tomorrow: see how Ultralight works for software teams 96 Live walkthrough of how SaMD and… | May 7, 2026 8:51 PM · 53 characters. Tomorrow: see how Ultralight works for software teams 96 Live walkthrough of how SaMD and… | |
| May 6, 2026 12:22 PM | Webinar tomorrow: How to avoid seeing your name published in an FDA warning letter | 83 | Webinar tomorrow: How to avoid seeing your name published in an FDA warning letter 96 It's… | May 6, 2026 12:22 PM · 83 characters. Webinar tomorrow: How to avoid seeing your name published in an FDA warning letter 96 It's… | |
| May 4, 2026 10:17 AM | Could your name end up in an FDA warning letter? | 48 | Could your name end up in an FDA warning letter? 96 This Thursday, Mike Drues breaks down… | May 4, 2026 10:17 AM · 48 characters. Could your name end up in an FDA warning letter? 96 This Thursday, Mike Drues breaks down… | |
| Apr 30, 2026 10:52 AM | Webinar: Live Walkthrough: Greenlight Guru for Software-Enabled Devices | 72 | Webinar: Live Walkthrough: Greenlight Guru for Software-Enabled Devices 96 Your dev team… | Apr 30, 2026 10:52 AM · 72 characters. Webinar: Live Walkthrough: Greenlight Guru for Software-Enabled Devices 96 Your dev team… | |
| Apr 29, 2026 12:37 PM | Webinar: How to avoid seeing your name published in an FDA warning letter | 74 | Webinar: How to avoid seeing your name published in an FDA warning letter 96 Mike Drues… | Apr 29, 2026 12:37 PM · 74 characters. Webinar: How to avoid seeing your name published in an FDA warning letter 96 Mike Drues… | |
| Apr 27, 2026 11:43 PM | eBook: Ultimate guide to modernizing your QMS before submission | 63 | eBook: Ultimate guide to modernizing your QMS before submission 96 Ultimate guide to… | Apr 27, 2026 11:43 PM · 63 characters. eBook: Ultimate guide to modernizing your QMS before submission 96 Ultimate guide to… | |
| Apr 22, 2026 11:13 AM | Tomorrow: How modern software teams develop compliant devices | 61 | Tomorrow: How modern software teams develop compliant devices 96 Last chance to save your… | Apr 22, 2026 11:13 AM · 61 characters. Tomorrow: How modern software teams develop compliant devices 96 Last chance to save your… | |
| Apr 21, 2026 12:14 PM | Whitepaper: Clinical evaluation under EU MDR: what it actually requires | 72 | Whitepaper: Clinical evaluation under EU MDR: what it actually requires 96 Clinical… | Apr 21, 2026 12:14 PM · 72 characters. Whitepaper: Clinical evaluation under EU MDR: what it actually requires 96 Clinical… | |
| Apr 20, 2026 10:31 AM | What's the cost of doing nothing about your QMS? | 48 | What's the cost of doing nothing about your QMS? 96 It may be more than you think. That… | Apr 20, 2026 10:31 AM · 48 characters. What's the cost of doing nothing about your QMS? 96 It may be more than you think. That… | |
| Apr 16, 2026 5:15 AM | Webinar: The non-BS QMS for software-enabled medical devices | 60 | Webinar: The non-BS QMS for software-enabled medical devices 96 A practical framework for… | Apr 16, 2026 5:15 AM · 60 characters. Webinar: The non-BS QMS for software-enabled medical devices 96 A practical framework for… | |
| Apr 8, 2026 10:18 AM | Virtual Summit: How Modern Software Teams Develop Compliant Devices | 67 | Virtual Summit: How Modern Software Teams Develop Compliant Devices 96 The compliance… | Apr 8, 2026 10:18 AM · 67 characters. Virtual Summit: How Modern Software Teams Develop Compliant Devices 96 The compliance… | |
| Apr 1, 2026 12:14 PM | Webinar: The Cost of Doing Nothing: Outgrowing Manual Quality Systems | 70 | Webinar: The Cost of Doing Nothing: Outgrowing Manual Quality Systems 96 The hidden cost… | Apr 1, 2026 12:14 PM · 70 characters. Webinar: The Cost of Doing Nothing: Outgrowing Manual Quality Systems 96 The hidden cost… | |
| Mar 21, 2026 12:15 AM | Whitepaper: FDA inspections under QMSR: the changes you need to be ready for | 77 | Whitepaper: FDA inspections under QMSR: the changes you need to be ready for 96 FDA… | Mar 21, 2026 12:15 AM · 77 characters. Whitepaper: FDA inspections under QMSR: the changes you need to be ready for 96 FDA… | |
| Mar 16, 2026 10:59 AM | Webinar: PMCF Data Collection: When Surveys Work, When They Don’t, and What Regulators Expect | 93 | Webinar: PMCF Data Collection: When Surveys Work, When They Don’t, and What Regulators… | Mar 16, 2026 10:59 AM · 93 characters. Webinar: PMCF Data Collection: When Surveys Work, When They Don’t, and What Regulators… |
Based on 87 emails received from Mar 16 to Nov 4, 2026. Times in US Eastern. How we collect