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From TypeLabs
TypeLabs presents Making Type Training Experiential with Hile Rutledge
In this program, Hile Rutledge of OKA will detail a number of training ideas, processing techniques and group exercises designed to expand a trainera ™s options in working with groups. Including a review of frequently asked questions in type training and a frank discussion of a what ifsa (the dreaded mistakes and unexpected exercise outputs that can arise when drawing on group
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In this program, Hile Rutledge of OKA will detail a number of training ideas, processing techniques and group exercises designed to expand a trainera ™s options in working with groups. Including a review of frequently asked questions in type training and a frank discussion of a what ifsa (the dreaded mistakes and unexpected exercise outputs that can arise when drawing on group
more...
From GlobalCompliancePanel
21 CFR Part 11 How to Successfully Prepare for and Host an FDA Inspection - Webinar By GlobalCompliancePanel
Overview: 21 CFR Part 11 is FDA regulation for electronic signatures and electronic records. It started by the pharma - it is a good regulation for medical and pharma companies but it is also a good guideline for other industries.
Why Should You Attend:
More and more organizations are striving to "go green" and develop "sustainable" organization's strategies, which almost always includes using
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21 CFR Part 11 Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar - Webinar By GlobalCompliancePanel
...or the scope of the inspection
o Some commonly asked questions by the inspectors and benefits of being compliant
* Module 3 - Internal and External Auditing for Part 11 Compliance
o Aspects of auditing for Part 11 compliance- starting at the audit program level and then going down on how to prepare for an audit to how to successfully execute the audit and follow up on
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How to Prepare and Submit a Bullet Proof 510k and Latest FDA Proposed Changes to the Process - Webinar By GlobalCompliancePanel
...thority to rescind 510(k)s, etc.
* 510(k) Frequently Asked Questions
* Attendees should be prepared to address any issues and challenges as experienced on behalf of their company in this open-forum and interactive session
Who will benefit: This course is appropriate to those involved in all aspects of the premarket notification, i. e., 510(k) process on behalf of medical device and
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