The Foreign Supplier Verification Program is an FDA program aimed at providing assurance that foreign suppliers of food and beverage products meet the same safety requirements as US-based companies, ensuring adherence to standards for public health protection including safety regulations, preventive controls and correct labelling. The Foreign Supplier Verification Program program is mandatory and applicable to importers of food to the US. Compliance is equal to a passport for your products’ entry into the US market.

The purpose of Foreign Supplier Verification Program provides us a way to get information about foreign suppliers to help ensure that they are meeting US safety requirement. More specifically, Foreign Supplier Verification Program requires that importers verify that their suppliers are producing food using processes and procedures that offer the same level of public health protection as the preventive controls requirements in the preventive controls and current good manufacturing practices rules for human food and animal food and produce safety. The FSVP rule requires importers to perform risk-based activities to verify that food imported into the United States is not adulterated.

GMP TRAINING is a requirement as it emphasizes employees performing all the tasks in accordance with GMP expectations and established procedures. GMP training is an essential requirement for pharmaceutical manufacturers.

GMP TRAINING help to ensure the consistent quality and safety of products by focusing attention on five key elements, which are often referred to as the 5 P’s of GMP—people, premises, processes, products and procedures.

The purpose of training in GMPs should be to ensure hourly employees perform their tasks as instructed and to motivate those employees to notify their supervisor:

• If they deviate from instructions.
• Observe a problem with equipment.
• Notice any material whose appearance is unusual, etc.

The underlying reason for GMP training is to ensure that the site and processes operate in a state of control. The excipient produced has a more consistent composition batch to batch, which assures reproducible performance of the excipient in the pharmaceutical application.

GMP TRAINING reminds the personnel that the site has procedures and directions that govern site operations. These documents assure that the operations are conducted consistently from person to person and in conformance with management directions.

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