Online Safety Community

Complaints, Adverse Event Reporting, and Recalls 2017

Event Details

Complaints, Adverse Event Reporting, and Recalls 2017

Time: July 27, 2017 at 9am to July 28, 2017 at 6pm
Location: Philadelphia, PA
Street: Hilton Garden Inn Philadelphia Center City
City/Town: Philadelphia, PA
Website or Map: http://www.globalcompliancepa…
Phone: 800-447-9407
Event Type: online, healthcare, training, courses
Organized By: NetZealous DBA as GlobalCompliancePanel
Latest Activity: May 12

Export to Outlook or iCal (.ics)

Event Description

Course "Complaints, Adverse Event Reporting, and Recalls - An Integrated Approach" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

 

Overview:

Medical Device manufacturers operate in numerous regulatory systems that often have different requirements and are not always consistent. The new ISO 13485:2016 emphasizes this problem. Manufacturers must identify their roles, identify the regulatory requirements for that role, and incorporate them into the quality management system.

               

Location:  Philadelphia, PA Date: July 27th & 28th, 2017 and Time: 9:00 AM to 6:00 PM  

 

Venue:  Hilton Garden Inn Philadelphia Center City

Address:  1100 Arch St, Philadelphia, PA 19107, United States

 Price:

 

Register now and save $200. (Early Bird)

Price: $1,295.00 (Seminar Fee for One Delegate)

Until June 10, Early Bird Price: $1,295.00 From June 11 to July 25, Regular Price: $1,495.00

Register for 5 attendees   Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*

Sponsorship Program benefits for “Complaints, Adverse Event Reporting, and Recalls Medical Device” seminar

At this seminar, world-renowned Medical Device subject matter experts interact with CXO’s of various designations. Executives who carry vast experience about Medical Device and Experts get down to discussing industry-related best practices, regulatory updates, changes in technologies, and much more relating to Medical Device.

As a sponsor of these seminars, you get the opportunity to have your product and company reach out to C-Level executives in Medical Device -related industries and become known among these elite executives and subject matter experts. Apart from being seen prominently at these globally held seminars, you also get talked about frequently in our correspondences with our experts and these participants.

For More Information- https://www.globalcompliancepanel.com/control/sponsorship 

 

Contact us today!

NetZealous LLC DBA GlobalCompliancePanel

john.robinson@globalcompliancepanel.com  

support@globalcompliancepanel.com 

Toll free: +1-800-447-9407

Phone: +1-510-584-9661

 Website: http://www.globalcompliancepanel.com

 

Registration Link – http://www.globalcompliancepanel.com/control/globalseminars/~product_id=900958SEMINAR?safetycommunity_july_2017_SEO

Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/

Like us our Facebook page: https://www.facebook.com/TrainingsAtGlobalCompliancePanel/

Follow us on Twitter: https://twitter.com/GCPanel

 

 

 

Comment Wall

Comment

RSVP for Complaints, Adverse Event Reporting, and Recalls 2017 to add comments!

Join Online Safety Community

Take our poll!

Take our poll!

Latest Activity

Roger Steven posted a blog post

HIPAA compliance for offshore vendors

In this age of outsourcing and globalization, and with it, the emerging potential phenomenon of the Internet of Things (IoT); it is quite a tempting proposition for HIPAA Business Associates or Covered Entities to think of outsourcing their processes relating to Protected Health Information (PHI). However, as is to be expected,…See More
17 hours ago
Adam Fleaming posted a blog post

Meeting equipment validation requirements from the FDA and EU

Putting in place a program for calibrating and maintaining test and measurement equipment is a regulatory requirement from both the FDA, under 21 CFR Part 210 and 211, and relevant EU regulations. Both these agencies have regulations that require this program from manufacturers.The purpose of this equipment validation program is to ensure these among others:o  The equipment is…See More
19 hours ago
Nakul Pratap joined HSE People's group
Thumbnail

HSE People

For anyone using www.hsepeople.com
yesterday
Nakul Pratap joined B. Kevin Stafford, Esq.'s group
Thumbnail

Construction Safety

All aspects of safety in construction!
yesterday

Forum

What's your favorite motivational/safety quote? 98 Replies

Favorite Motivational Quote: If you want something, you'll find a way - If not, you'll find an excuse.Favorite Safety Quote: Don't learn safety by accident!Continue

Started by Michelle Sears. Last reply by David R Snell Apr 26.

Feedback on a injury prevention product we're building.

Hi everyone!For full transparency ill tell you a little about myself and what I hope to accomplish. My name is Zuber and I'm an engineering student who founded a startup helping to build wearable…Continue

Tags: product, prevention, injury, back, safety

Started by Zuber Ahmed Apr 24.

Best overall personal safety book? 1 Reply

What do you think is  the best all-in-one book out there for optimizing personal safety and the safety of one's family?  Right now I have …Continue

Started by David R Snell. Last reply by David R Snell Apr 21.

Fire codes for residential buildings

Hi,Can anybody kindly give me a hint how to find Fire Codes for residential buildings in different cities in the United States?Continue

Started by Darren Asad Apr 14.

OSHA and Machine Guard Door Safety???

We have what we feel is not a unique situation and were wondering if anyone might of run across this challenge and know more about the requirements.  We are building a small machine system that…Continue

Tags: electric, osha, air, door, interlocked

Started by Scott V Mar 24.

Badge

Loading…

© 2017   Created by Safety Community.   Powered by

Badges  |  Report an Issue  |  Terms of Service