The Cutting Edge of Medical Technology Content, Community & Collaboration
July 21, 2016 from 11am to 12pm – Online Join the speaker to learn more about: The current state of safety reporting and why it has been confusing Available solutions and the challenges they still pose Qualities of an ideal safety partner… Organized by Xtalks Life Science Webinars | Type: webinar
July 21, 2016 at 9am to July 22, 2016 at 6pm – Chicago, IL Course "HIPAA for the Compliance Officer" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: I will be going in… Organized by Netzealous -MentorHealth | Type: seminar
July 19, 2016 from 1pm to 2pm – Online Description: “The goal is to transform data into information, and information into insight” - Carly Fiorina, former President of Hewlett Packard Too often we make an art form out of collecting data,… Organized by Compliance Trainings | Type: webinar
July 19, 2016 from 1pm to 2pm – Online Manufacturers and importers must report adverse events associated with a risk to health or death. Until now, the reports were submitted in hardcopy using MedWatch form 3500A. Managing the volume adve… Organized by Compliance Trainings | Type: webinar
July 19, 2016 from 1pm to 2pm – Online In this webinar the speakers will discuss why Tissue Phenomics is represented as a novel technique to discover relevant patterns in tissue slides that predict drug response or other clinical outcomes. Organized by Xtalks Life Science Webinars | Type: webinar
July 19, 2016 from 11am to 12pm – Online In this webinar, the presenter will show how pharmaceutical packaging and labeling complexity occurs, what the consequences are of inaction, and most importantly, what pharmaceutical companies can do… Organized by Xtalks Life Science Webinars | Type: webinar
July 15, 2016 from 1pm to 2pm – Online We will discuss the importance of establishing a data governance framework and program for data that is collected, analyzed, stored or reported using a computer system subject to FDA regulations. A d… Organized by Compliance Trainings | Type: webinar
July 14, 2016 from 1pm to 2pm – Online Description : “Good documentation practices” is a “current” industry practice that is reviewed and cited by federal regulators when audited. Pharmaceutical/Biological document are legal documents tha… Organized by Compliance Trainings | Type: webinar
July 14, 2016 from 12pm to 1pm – Online In this webinar, the speaker will discuss the fundamental differences in conducting research in pre-market randomized controlled trials (RCT) versus post-approval. Organized by Xtalks Life Science Webinars | Type: webinar
July 14, 2016 at 9am to July 15, 2016 at 6pm – San Diego, CA Course "Validation and 21 CFR 11 Compliance of Computer Systems: Intermediate to Advanced" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification u… Organized by Netzealous -MentorHealth | Type: seminar
| S | M | T | W | T | F | S |
|---|---|---|---|---|---|---|
| 1 | 2 | 3 | 4 | 5 | 6 | 7 |
| 8 | 9 | 10 | 11 | 12 | 13 | 14 |
| 15 | 16 | 17 | 18 | 19 | 20 | 21 |
| 22 | 23 | 24 | 25 | 26 | 27 | 28 |
| S | M | T | W | T | F | S |
|---|---|---|---|---|---|---|
| 1 | 2 | 3 | 4 | 5 | 6 | 7 |
| 8 | 9 | 10 | 11 | 12 | 13 | 14 |
| 15 | 16 | 17 | 18 | 19 | 20 | 21 |
| 22 | 23 | 24 | 25 | 26 | 27 | 28 |
| 29 | 30 | 31 | ||||
© 2026 Created by CC-Conrad Clyburn-MedForeSight.
Powered by