For many food products, validating and verifying a process sounds like a simple task if the product has been made for years and is considered very safe.
Does your food safety system employ a systems engineering approach? If not, maybe it should.
The Food Safety Modernization Act will modernize current Good Manufacturing Practices regarding manufacturing, processing, packaging and holding of human foods.
Audits should include the live sampling of heat transfer fluids to ensure the safe processing of foods.
Nestlé S.A., which has operations in 197 countries with 339,000 employees, has expanded its dairy factory in Jalisco, Mexico, transforming it into the company’s first “zero water” manufacturing site in the world.
Hazard Analysis and Critical Control Points (HACCP) was originally developed based on several key program types.
The final FSMA regulations on preventive controls for animal food are published—what does it mean for your company?
Employee attitudes toward specific behaviors have been identified as predictors for overall employee behaviors and food safety.
Thermal imaging cameras can improve food safety while simultaneously working to limit the current rate of energy consumption. How can this technology benefit your company? Read the article and learn how.
Validation, verification and monitoring are critical components of food safety and quality management programs.
Companies delivering high-quality nutritional beverage products to consumers face many obstacles that can be overcome using standardized processes and practices.
The use of recycled materials in food packaging applications is governed by the same principles that apply to all food packaging.
Anritsu recently debuted Detection360™, a proprietary process to advance quality control programs and ensure superior ROI by securing all points of detection within the processing environment, while also reducing risks associated with unwanted contaminants or missing items in a company's products.
Washing cannot always make leafy greens safe, so the concept of homogeneity in all microbial testing is critical for the ability of samples to represent the lot.
New regulations mark the first time that packaging operations will come under the regulatory microscope in a significant way.
Without clear standards regulating labeling definitions, food and beverage companies are finding themselves under greater scrutiny over the validity of what is found on their products’ labels.
The bottom line is that the internal audit program like ISO 22000 is a systems approach to verifying that procedures are being followed as documented.
Minimizing packaging waste must be done in a way that maintains the safety and hygiene of the food to keep it safe.
The who, how, what, where, when and why to sample are critical to control the risks of biological contamination.
ISO 22000 is a nonprescriptive standard that provides both opportunities and challenges to organizations that desire to implement the requirements.