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Quality System Regulations for Drugs, Devices, and Tablets and How to generate your DMF - 2-day In-person Seminar

Event Details

Quality System Regulations for Drugs, Devices, and Tablets and How to generate your DMF - 2-day In-person Seminar

Time: May 21, 2015 at 9am to May 22, 2015 at 6pm
Location: Boston, MA
Street: Boston, MA
City/Town: Boston, MA
Website or Map: https://www.globalcompliancep…
Phone: 18004479407
Event Type: food, fda, medical, device, defence, and, navy, aerospace, mining
Organized By: GlobalCompliancePanel
Latest Activity: Feb 24, 2015

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Event Description


Primary Student Objectives - General High Level Topics where we will move down to very specific discussion and details to generate a much higher comprehension for quality individuals even though during this course you will not have to take a final exam!

Upon completing this course participants will gain a much better Quality Systems comprehension, based on the instructor's decades of experience helping generate quality system regulations, working with the FDA, fixing FDA findings and generating a synergistic discussion with the attendees to help us all make sure we understand that there is rarely ever on "one" way to do things or "right and wrong", just like making an assumption about the Root Cause of an incident rather than working together to realize there are other things that took place that the individual making the assumption may not have been aware of.

1. What is expected from the QA professional and how other industries (FAA, ISO, EPA, etc.) have made Quality Systems so profitable by having the Head of Operations and the Head of Quality trading places every 6 months.

2. Gaining a more practical Comprehension from experience of the Quality Systems regulations not just reading and thinking you are an expert (reading three books on how to ride a bicycle does not make you an expert).

3. Once we have a better perspective then we will identify the necessary activities like working on a thesis to generate the needed performance for the entire Quality System.

4. How to apply current technology to generate the objective evidence needed to generate the attitude of making the FDA successful when inspecting by answering all the potential inspector questions before asked. Use the applicable technology to think like an FDA inspector

5. How are we going to maintain documented evidence to prove that the process and initial validation is still working in accordance with the Quality System regulations

6. Make sure we have the proper tools and comprehension to perform the needed internal audits which ensures that when a client audits the company or the FDA inspects the facility, we have already been doing all the things they might be reviewing.


Mr. Jerry Dalfors has extensive (40+ years) of business administration, consultative, technical and managerial experience in the development and manufacture of highly regulated biopharmaceutical products including injectables, biologics, medical devices and oral dosages. He has held permanent employee, temporary employee and company representative management positions with a multitude of the major pharmaceutical and biotechnology companies in the US. 

Price: $1,295.00 

Quick Contact:

NetZealous BDA as GlobalCompliancePanel

USA Phone:1-800-447-9407
Fax: 302-288-6884

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