In-house Training Seminars
(Inhouse Training Inquiry Form)Noblitt & Rueland offers private in-house or on-site training courses 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 director(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.
Please use the following general course web page links (ignore the dates, number of speakers, and locations as these are links to our public offerings) as reference when considering in-house training programs. 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 714-258-4646.
Course Titles/Topics:
or call 714-258-4646 or e-mail for details!
Courses are offered in condensed one day (full day) programs so that time away from the job and other commitments can be minimized. An optional workshop day allows 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 considerable accellerate a project.
Each participant receives a professional binder of course materials and a certificate awarding Continuing Education Units (CEU) that can be used to document employee training and competency per FDA GMP and ISO 13485. The company will receive a training report documenting the training and everyone in attendance and will also receive several CD's packed with FDA & international regulatory information and guidance.
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. Travel schedules for our course directors are rigorous and sometimes makes it difficult to schedule courses with short notice. However, do not delay in contacting us as sometimes short notice requests can sometimes be accommodated. For more information including a price schedule please use our On-line Request Form or e-mail or call us at 714-258-4646.
*Confidentiality Agreements will be signed by our course directors upon request.
5405 Alton Parkway 5A, #530 Irvine, California 92604-3718 USA Telephone (714) 258-4646 Facsimile (714) 258-3990