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All aport’s specialist laboratory relocations adopt GxP compliance standards.

Unlike other providers in the laboratory relocations industry, all our services meet GxP requirements, including Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP). Aport’s high standards and commitment to best practice help set us apart as an industry leader.

We understand that effective GxP compliance is essential to ensuring a seamless laboratory relocation which meets all the necessary regulations. And every member of our staff shares our vision to provide a service which not only meets the requirements of our clients, but exceeds them.

For each individual aport project, clients’ exact needs regarding GxP will be discussed in detail and thoroughly planned. 

Aport invests a significant amount of time and money in training all laboratory relocation staff to operate in a facility which is GLP or GMP classified. All the training employees undertake in this area as well as our responsibilities, is documented and records can be provided on request.

We also operate GxP policies regarding the handling and transporting of investigational drugs, biological samples and ancillary supplies.

To ensure GxP adherence at all times, we are careful to use appropriate packaging materials and specialist vehicles, which are temperature-controlled if necessary, during the relocation process. All materials along with every item of laboratory instrumentation is carefully logged, labelled and then handled according to a stringent set of procedures.

Aport will provide your organisation with full validation reports which can be included in dossier submissions to the FDA, EMA and other agencies.

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