731 901 601
GMP+ and feed transport – requirements that are often overlooked

GMP+ and feed transport – requirements that are often overlooked

Feed transport is one of the most sensitive stages in the entire supply chain. Even if a product leaves the factory in a fully safe condition, inappropriate transport conditions can quickly lead to contamination or a deterioration in quality. In the GMP+ system, transport is therefore not an afterthought, but an integral part of safety management.

Who is responsible for ensuring transport complies with GMP+?

The GMP+ requirements apply not only to transport companies but also to the clients, i.e. feed manufacturers and traders. This means that responsibility is shared – the carrier must meet specific standards, but it is the company commissioning the transport that should ensure it is working with a suitable partner.

This necessitates the qualification of transport providers. The company should check whether a given operator holds a GMP+ certificate or an equivalent one, and if not – whether it meets the requirements through appropriate procedures and contracts. An often-overlooked aspect is the formal documentation of this verification.

Cleanliness and cargo history – crucial, yet often neglected

One of the most common sources of problems is a lack of control over so-called previous loads. GMP+ clearly stipulates that means of transport must be suitable for the carriage of feed, and their history must not pose a risk of contamination. This boils down to the need to:

  • check what was previously transported,
  • use lists of permitted and prohibited loads,
  • document the vehicle cleaning process.

A statement from the carrier alone is not always sufficient. In many cases, specific records are required, for example in transport documents or cleaning log systems. The absence of this information is one of the most common non-compliances detected during audits.

Documentation and supervision of transport

GMP+ places great emphasis on traceability, which is why transport must be properly documented. It must be possible to trace every batch of feed – from the point of loading right through to the consignee. The requirements include, amongst others:

  • linking transport documents to a specific batch of product,
  • retaining information on the date, means of transport and carrier,
  • monitoring transport conditions (e.g. protection against moisture or contamination).

An aspect that is often overlooked is the supervision of transport whilst in progress. In the case of longer journeys or international transport, it is worth taking into account procedures for dealing with emergencies, such as damage to the load or a change in the means of transport.

The most common mistakes made by companies in the transport sector błędy firm w obszarze transportu

Many non-compliances with GMP+ stem not from a lack of knowledge, but from a failure to pay attention to detail. The most common problems include: carriers lacking up-to-date qualifications, incomplete vehicle cleaning records, failure to verify previous loads, and overly general provisions in transport contracts. Another problem is the assumption that responsibility lies solely with the transport company. However, GMP+ auditors assess the entire system – including how the company supervises its partners.

Such shortcomings can result not only in non-compliance during an audit, but also in a real risk of product contamination and a loss of customer trust. It is therefore crucial to implement consistent procedures for supervising transport and to review them regularly. It is particularly important to systematically document activities and clearly define responsibilities on both sides of the partnership.

If your organisation is planning to obtain certification, it is worth familiarising yourself in advance with the GMP+ implementation process and the scope of activities required to meet the standard’s requirements.

 

Read other posts

A laboratory without ISO/IEC 17025 accreditation loses contracts before it even has a chance to submit a bid

A laboratory without ISO/IEC 17025 accreditation loses contracts before it even has a chance to submit a bid

The laboratory services market is changing faster than most laboratories realise. Just a few years ago, ISO/IEC 17025 accreditation was a distinguishing feature – proof of exceptional quality that opened doors to the most demanding clients. read more
The EUDR, logistics and customs – what is changing in the trade of goods?

The EUDR, logistics and customs – what is changing in the trade of goods?

The introduction of the EUDR has a significant impact not only on businesses’ obligations within the supply chain, but also on the way logistics and customs clearance operate. read more
ISO 9001 and ISO 27001 in healthcare facilities – how do these certifications translate into points in the National Health Fund (NFZ) tender?

ISO 9001 and ISO 27001 in healthcare facilities – how do these certifications translate into points in the National Health Fund (NFZ) tender?

For many medical facilities, a contract with the National Health Fund (NFZ) is the foundation of their operations. read more
More posts