Staff Recruitment and Internal Training Development
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21 CFR 111 regulations require the appropriate GMP training in a facility for personnel to be conducted on a regular basis.
Tuesday 18 to Wednesday 19 September 2025
Carlsbad, California
$1295.00 per delegate
$1,165.50 (Early bird booking)
Type: Dietary
About this course
21 CFR 111 regulations require the appropriate GMP training in a facility for personnel to be conducted on a regular basis. The options for meeting this regulatory requirement include having expert consultants on-site to conduct the training on a regular basis, send personnel to external courses for training and/or develop and conduct an internal training program to meet the regulatory requirements.
This course will provide you with the insight into developing training materials, schedules and provide insights into how to integrate a culture of “quality” into your organization. Tools and resources will be provided so that delegates can implement a “quality” training program in their facility.
A company’s most precious assets are its people. Training is essential for the maintenance of high standards of quality assurance and GMP. This undeniable fact is forcefully stated by all the regulatory agencies. In the Dietary Supplement GMPs (21 CFR Part 111):
21 CFR Part 111.14(a) “You must have qualified employees who manufacture, package, label, or hold dietary supplements.”111.14© “Each person engaged in manufacturing, packaging, labeling, or holding, or in performing any quality control operations, must have the education, training, or experience to perform the person’s assigned functions.”
Who Should Attend
The training is designed for QA/QC managers, R&D managers and personnel, product developers, analytical method developers and laboratory personnel, quality system auditors and staff, and regulatory personnel.
Course outline
What You Will Learn
- Insight into developing training materials, schedules and provide insights into how to integrate a culture of “quality” into your organization
- Position descriptions, recruiting and hiring
- Training and development concepts and practice/training evaluation
- Record keeping and updating training
Discussion and Working Groups
A significant proportion of the course time will be devoted to group work, where delegates have the opportunity, through case studies, to put theory into practice.
Additionally, discussion periods will provide delegates with plenty of time to obtain answers to their specific questions and concerns.
Venue
Carlsbad, California
Hyatt House Carlsbad (formerly known as Summerfield Suites)
Hyatt House San Diego/Carlsbad
5010 Avenida Encinas
Carlsbad, California 92008
United States
Located on the coast of beautiful Carlsbad, California and conveniently situated only 2½ blocks from the beach, HYATT house™ San Diego/Carlsbad is surrounded by the area’s many great attractions. Enjoy a five-minute shuttle ride to Legoland or the Village of Carlsbad or travel a short 35 miles to the San Diego Convention Center, SeaWorld, San Diego Zoo, San Diego Wild Animal Park, Old Town or the San Diego airport.
Hotel Accommodations
For more information on special room rates, please contact the Hyatt House at 760-929-8200 and mention NSF-DBA training. Special rates may be available for up to 30 days in advance of the training session.
Tutors
We believe that our team of experts are the best available. Not only have they got years of experience in the industry, but they are committed to tutoring and helping those inside the industry to improve and raise the standards. We understand that you attend courses to learn about the latest regulations and to get your questions answered.
Our expert for this course is:
What you've said
“NLI is always working to implement the most stringent quality systems and looking for opportunities to prove the superiority of its systems. DSQP certification with NSF-DBA has been another way for NLI to show a commitment to being a CMO of the highest quality. Investment in training ensures your company is in compliance and manufacturing safe products for the public”
Jera’le Smith, Director of Quality Assurance, Nutritional Laboratories International (NLI)
“I attended both NSF-DBA’s FDA inspection Readiness and Corrective Action Management modules and our company assiduously implemented the recommendations made. I am absolutely convinced that doing so was one of the primary reasons our company did not receive an FDA Form 483 following an FDA unannounced 4-day GMP inspection”
Kim Randall Pearson, General Counsel, Thorne Research, Inc.
An NSF International Company