Food Safety
and cGMP Consulting

EMMA International’s food safety consulting service supports food manufacturers in a variety of areas to ensure compliance with food safety regulations and standards.

No matter how big or small your project is, our experts are here to support you with all aspects of compliance for your food manufacturing operations. We have capabilities in all facets of food production and processing, including beverage, bottled water, infant formula, acidified foods, and medical foods.

Whether you are looking to comply with ISO 22000, need support with FDA/EPA regulations, or are looking for guidance with the Food Safety Modernization Act (FSMA), let our in-house Preventive Control Qualified Individuals (PCQIs) guide you every step of the way!

 

Overview of Food Safety Consulting Services

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Food Label Reviews

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Recall support

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HACCP Plan Development

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Mock Inspections and Audit Readiness Training

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Food Defense & Facility Consulting

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Food Safety

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483 and Warning Letter Remediation

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cGMP and FSMA compliant QMS Development

Specialty Areas

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Low-Acid Canned Foods

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Medical Foods

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CBD Infused Foods

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Infant Formula

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Bottled Water

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Food Allergens

Ready to learn more about working with us?

Food Safety/GMP 

HACCP Plans

HACCP Plans

The Food and Drug Administration (FDA) better protects the public health by aiding the food supply's safety and security in the Food Safety Modernization Act (FSMA). This act allows the FDA to write and regulate food safety rules that prevent food safety issues rather than detecting and reacting to issues after they occur.
The FDA’s Proposal for a Unified Human Foods Program

The FDA’s Proposal for a Unified Human Foods Program

Ever since FSMA was signed into law in 2011, there hasn’t been another major reform for food safety; the HFP is looking to change that. Coupled with the massive reorganization of the ORA, which will end up being the largest re-org in FDA history, the HFP is aiming to modernize and streamline the way the FDA governs both human and animal food products.
Complying with HIPAA during Clinical Trials

Complying with HIPAA during Clinical Trials

Most people are familiar with, or have at least heard of, the Health Insurance Portability and Accountability Act (HIPAA). HIPAA was passed in 1996 to establish rules regarding Protected Health Information (PHI) for patients in the US. The three main rules are The Privacy Rule, The Security Rule, and the Breath Notification Rule, which all revolve around how PHI is handled, disclosed, and breach risks are mitigated. So, how do sponsors actually ensure they are complying with HIPAA during clinical trials?

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