WEBINARS

 

Food and Dietary Supplements Manufacturing and Contamination Control Regulatory Compliance Training - Live Webinars, Recordings & CDs

Navigating Standard 1.2.7 - The Regulation of Nutrition and Health Claims in Australia/NZ

webinar-speaker   Janine Curll

webinar-time   90 Min

Product Id: 704692

This training program will discuss what is a NCC (Nutrition Content Claims), a GLHC (General Level Health Claims), a HLHC (High Level Health Claims), and the conditions for making these claims. Attendees will understand the conditions on the types of foods that can carry nutrition content and health claims and the process to self–substantiate a food health relationship and requirements for FSANZ notification.

Recording Available

* Per Attendee $199

 

5 Steps to Creating a Rock-Solid Recall Plan

webinar-speaker   Valerie Scheidt

webinar-time   60 Min

Product Id: 704720

This training session is designed for food safety practitioners who are preparing for implementation of the Preventive Controls rule, and require assistance in effectively developing a recall plan. Those who have an existing product recall and crisis management program understand that identification of the issue is only the first step in controlling the problem. Operations which have formally relied upon the standards as set forth by certification bodies may wish to reconsider their approach based upon the finalization of the PC Rule.

Recording Available

 

Performing an Effective Risk Assessment of Potential Breaches

webinar-speaker   Frank Ruelas

webinar-time   60 Min

Product Id: 704682

The Health Insurance Portability and Accountability Act (HIPAA) rules and regulations clearly state that an impermissible use or disclosure is presumed to be a breach. Therefore, any such incident triggers the required notifications. However, if an organization performs a risk assessment and shows why the incident is not a breach, the required notifications would no longer apply. This training program will focus on how to perform an effective risk assessment that can not only reduce the administrative burden of dealing with presumed breaches, but also help an organization meet other criteria such as those that exist in the Office for Civil Rights HIPAA audit protocol.

Recording Available

 

Global Considerations for Supplements and Nutritional Products

webinar-speaker   James Russell

webinar-time   90 Min

Product Id: 704666

This training program will discuss global considerations for supplements and nutritional products as well as the country/region specific considerations for them. It will also elaborate healthcare authorities’ outlook, global expansion challenges, product classification, and marketing challenges in the industry.

Recording Available

 

Good Laboratory Practices for Food Manufacturing

webinar-speaker   Melinda Allen

webinar-time   90 Min

Product Id: 702539

This 90-minute webinar will show how you can apply FDA's Good Laboratory Practices in a food quality laboratory setting. It will review differences, highlight specific needs of a food lab and provide guidelines for implementation.

Recording Available

* Per Attendee $229

 

Don't Fear the Fork: 7 Strategies for Effective Allergen Control

webinar-speaker   Valerie Scheidt

webinar-time   60 Min

Product Id: 704637

This training program is designed for food safety practitioners who are preparing for implementation of the Preventive Controls Rule, and require assistance in effectively managing allergens. Those who have an existing allergen control program realize that though a plan is in place, compliance and ongoing monitoring is essential for success. Operations which have formally relied upon the standards as set forth by certification bodies may wish to reconsider their approach based upon the finalization of the PC Rule.

Recording Available

 

2 Ways to Look at Vulnerability Assessments - Part 1 and Part 2

webinar-speaker   Ned Mitenius

webinar-time   60 Min

Product Id: 704471

This training program is designed for food defense and food safety practitioners who are preparing for implementation of the Intentional Adulteration rule. Those who have existing Food Defense Plans should understand how the vulnerability assessment requirements may go beyond most existing food defense plans and what considerations will be needed to comply with the rule. Operations which have relied on the FDA supplied Food Defense Plan Builder software tool should know the limitations of the existing tool, and how to overcome them, and who is qualified to do so.

Recording Available

 

Creating FDA-compliant cGMP Training Program

webinar-speaker   Henry Urbach

webinar-time   60 Min

Product Id: 703401

This webinar will explain how to implement an effective and FDA compliant GMP training program. It will discuss regulatory requirements and expectations for a well-trained workforce.

Recording Available

* Per Attendee $179

 

Food Defense - Is your organization safe?

webinar-speaker   Jason Teliszczak

webinar-time   60 Min

Product Id: 703271

This food defense webinar will detail what an organization needs to have in place in order to safely manufacture, package, and or handle food products. It will cover a broad range of production types, facilities, and the transportation of goods. This webinar will highlight key areas of the organization that need to be controlled to ensure that intentional contaminants do not enter the product by potential threats.

Recording Available

* Per Attendee $199

 

Monitoring for the FSMA Proposed Rule on Intentional Contamination

webinar-speaker   Ned Mitenius

webinar-time   60 Min

Product Id: 704451

The program will discuss the practical development of an adequate monitoring program optimized to fit the Intentional Adulteration Rule. Attendees will learn the difference between monitoring, verification and validation. The program will review the existing Food Defense Plan Builder tool including its limitations and some possible changes. In the absence of a provided tool, the program participants will be shown how to create an effective monitoring program, and the documentation required to support it.

Recording Available

 

Emerging Issues in Food Safety - Locally, Nationally and Globally

webinar-speaker   Michael Brodsky

webinar-time   60 Min

Product Id: 704518

This training program will focus on understanding and accepting our respective responsibilities to help ensure that our food supply is safe by pursuing a food safety culture locally, nationally and globally.

Recording Available

 

Microbiological Risk: Do I Really Need to Test Raw Materials for Microorganisms

webinar-speaker   Henry Urbach

webinar-time   60 Min

Product Id: 702635

This webinar will cover the regulatory perspective in testing raw materials for microorganisms and how you can manage the risk of raw materials being the major source of microbial contamination in your medical product manufacturing process.

Recording Available

* Per Attendee $229

 

Record Keeping for a food Recall: Keeping Records to Minimize the Affect of a Recall

webinar-speaker   Craig Nelson

webinar-time   60 Min

Product Id: 701119

This Food safety training will provide valuable guidance to management, supervision, and quality staff that are involved with record keeping for product and ingredient traceability and recall.

Recording Available

* Per Attendee $199

 

Record Keeping for the Bioterrorism Act: Meeting and Exceeding the Requirements in a Simple Manner

webinar-speaker   Craig Nelson

webinar-time   60 Min

Product Id: 701318

This Bioterrorism act training will provide the attendee a clear understanding of what is expected, how an investigation will proceed, and how to keep records that will minimize the impact of an incident.

Recording Available

* Per Attendee $299

 

HACCP in a Real World Environment

webinar-speaker   John Miller

webinar-time   60 Min

Product Id: 701173

This HACCP training will explain the FSIS regulations and policies program requirements.

Recording Available

* Per Attendee $50

 

Rules of Practice (FSIS) 9CFR part 500

webinar-speaker   John Miller

webinar-time  

Product Id: 701172

This Food Safety and Inspection Service (FSIS) training will guide you through the different levels of enforcement that FSIS utilizes.

Recording Available

* Per Attendee $199

 

Critical Control Points (CCP’s). Where are they? Why? When?

webinar-speaker   Irwin Pronk

webinar-time   60 Min

Product Id: 701180

This Food safety compliance training will explain the CCP Decision Tree and help you understand the principles behind each question. We will review various food processing steps in a variety of situations to determine whether they are CCP’s. What is the thought process in determining a CCP? Can it be done consistently? What criteria are used? Are some processing steps always CCP's e.g. heating? If not, why? One thing to remember is the importance of analyzing the hazards at each step very carefully. The more clearly the hazards are described (including equipment failures, personnel errors etc) the easier it will be to find the CCP.

Recording Available

* Per Attendee $199

 

The CAPA Trap or Common Problems and Pitfalls

webinar-speaker   Jeff Phillips

webinar-time   60 Min

Product Id: 700914

The following webinar will cover common CAPA problems across industries and how to avoid them. This webinar will provide valuable assistance to all regulated companies that need to have CAPA systems as mandated by the FDA.

Recording Available

* Per Attendee $249

 

Applying HACCP to insure compliance

webinar-speaker   Joyce Wilkins

webinar-time   60 Min

Product Id: 700466

This HACCP training will equip the student to apply the concepts of HACCP in their food operation in a manner that is useful and effective without being unduly burdensome. Although HACCP has been around for over 40 years, it still remains the standard in designing a food safety program.

Recording Available

* Per Attendee $149

 

Getting to Know FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies

webinar-speaker   Kenneth Christie

webinar-time  

Product Id: 703635

This training program will provide attendees with a better understanding of how the FDA conducts their audits and the areas of most focus. In addition, it provides a summary of common GMP deficiencies given to drug manufacturers, to use to evaluate one’s own practices. Finally, when given a regulatory audit finding, this webinar will review the top five items to remember when submitting your responses to them to avoid further questions.

Recording Available

 

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