Medical Device Companies: Join us for a free Webinar on Wednesday, December 3
Title: MassMEDIC Webinar: Using Technology to Streamline EH&S Data Management Date: Wednesday, December 3, 2014 Time: 12:00 PM – 1:00 PM EST After registering you will receive a confirmation email containing information about joining the Webinar.
Space is limited. Reserve your Webinar seat now at: https://www4.gotomeeting.com/register/694302183
The year is coming to a close and that means it’s time to start gathering data for environmental, health and safety (EH&S) regulatory reports due in 2015. Have you set yourself up to easily have the data readily available for EH&S regulatory reports or corporate sustainability reports?
Medical device companies are required by federal, state, local, and even global EH&S regulatory agencies as well as non-governmental stakeholder commitments (such as ISO 14001 and OHSAS 18001) to maintain EH&S records and monitor many aspects of their operations. These demands create an on-going challenge to organize, manage, and standardize all of the EH&S data. Harnessing the full potential of readily available technologies such as smart phones, tablets, and the cloud can make a significant difference in streamlining EH&S systems.
This webinar will provide examples of how available technologies can eliminate duplication, time-consuming data collection and analysis, and inefficiencies in communication of important information. We will also discuss some common data management challenges faced by medical device companies and share some of technologies and solutions that streamline these processes and additional systems that are being developed to assist with future needs. Lastly, we will provide an overview of the EH&S requirements which will affect Medical Device Companies in 2015.
Be ready for the upcoming year and its EH&S regulatory submittals, sustainability reports, and reports that show continual improvement of your environmental management system.
Presenters: John Baycroft, Sr. Environmental Engineer, Solutions Coordinator, CAPACCIO Linda Swift, CHMM, TURP, CET, RABQSA Auditor Practice Area Leader for Medical Device Industry, CAPACCIO Moderator: Tom Sommer, President, MassMEDIC
System Requirements PC-based attendees Required: Windows® 8, 7, Vista, XP or 2003 Server
Mac®-based attendees Required: Mac OS® X 10.6 or newer
Mobile attendees Required: iPhone®, iPad®, Android™ phone or Android tablet
For more information, please contact Linda Swift at 508-790-0033 ext. 119 or firstname.lastname@example.org.