On-Site or Virtual Training Seminar List & Info

Request for Proposal

(*You may also call 1-949-398-5222 or email info@fdaconsulting.com )

Please either fill out an On-Site or Virtual Training Inquiry Form , phone 1-949-398-5222 or send an e-mail to info@noblitt-rueland.com to quickly send us an inquiry regarding your training needs so we may provide you with an estimate or proposal. We will be happy to discuss your training needs with you.

Noblitt & Rueland offers private in-house training courses conducted on-site or virtually on regulatory, quality, technical, and management issues. Entire product teams and companies can be trained at one time assuring the understanding and efficient implementation of new processes, philosophies, requirements, and regulatory compliance issues into an organization. An in-house course allows for smaller more intimate discussions specifically addressing the needs of your organization. In-depth, detailed discussions occur without risking confidentiality*. Participants hear the same message and discuss issues together, allowing them to more efficiently integrate the concepts learned into everyday operations. This is especially helpful for cooperative integration of concepts across departmental boundaries. You control the environment with courses being held at a location of your choosing. Prior discussions with the course instructor(s) help customize the course to focus on specific areas that may require attention. Pricing for each course is based on the number of days, the number of speakers, and the number of participants involved.

Courses can be customized upon request; however, over 90% of our in-house programs presented do not need customization. For other topics and pricing please use our On-line Request Form or e-mail or call us at 1-949-398-5222.

Course Titles/Topics:

On-Site or Virtual Training Inquiry Form

or call 949-398-5222 or e-mail for details!

On-site courses are typically offered in condensed one day (full day) courses so that time away from the job and other commitments can be minimized. Virtual courses can be taught over multiple days, e.g. 4 hours per day for 2 days. Optional workshop days allow the attendees to work on topic related examples specific to the company, such as new projects or products to be developed, and result in useable work product being produced which can considerably accellerate a project.

An optional assessment (test/quiz) will be administered allowing each participant to receive a certificate awarding Continuing Education Units (CEU) that can be used to document employee training and competency per FDA GMP/QSR and ISO 13485. A professional binder of course materials and handouts will be made available electronically with print copies available as an option. The company will receive a training assessment report documenting the training and everyone in attendance which will be helpful during a regulatory audit by FDA or your notified body.

As an additional option, you may want to consider follow-up or preparatory consulting (documentation and procedure reviews, etc) or an independent compliance audit either before or after the course so that you can obtain a baseline for improvement to your company's current compliance with regard to regulatory requirements. An estimate of the time required and hourly rates will be provided at your request. If you desire to schedule an in-house course, please contact us as soon as possible. For live on-site training, travel schedules for our course directors are rigorous and can make it difficult to schedule courses with short notice. However, do not delay in contacting us as sometimes short notice requests can be accommodated. For more information including a price schedule please use our On-line Request Form or e-mail or call us at 1-949-398-5222.

*Confidentiality Agreements will be signed by our course directors upon request.

 

Contact Information:

Noblitt & Rueland
5325 Alton Parkway C-530
Irvine, CA 92604
USA
Phone: 1-949-398-5222
E-mail: info@fdaconsulting.com