Fr/En
Radiochemistry & FDG Production Area_Cross Cancer Institute

The project consisted of a review of the radiochemistry production facility, operations, equipment and utilities for cGMP compliance, and a preliminary study for the upgrade of the facilty within the existing operating area.

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Radiochemistry & FDG Production Area_Hamilton Health Sciences Centre

The project consisted of a review of the existing radiochemistry production area for cGMP compliance, and the preparation of a Basis of Design and execution plan to construct and validate a stand-alone clean room within the existing building for the manufacturing and dispensing of FDG, and the integration of new process equipment.

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Radiochemistry & FDG Production Area_Montreal Neurological Institute

The project consisted of upgrading the existing FDG production area to ensure that the operations, facility, and documentation are compliant to the latest cGMP guidelines and CNSC regulations.

Following the completion of the project, the PET centre successfully passed an audit by Health Canada in April 2010.

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Radiopharmaceutical Laboratories_Draximage

The project consisted in the preparation of a feasibility study for the project, followed by the supervision of design, construction, and validation of a 20,000 ft2 high level radiopharmaceutical production laboratory within an existing warehouse area for the preparation of imaging radioisotopes.

The project was executed in two phases, with Phase 1 being a 10,000 ft2 laboratory on the ground floor, and a Phase 2 expansion of a similar sized area above Phase 1.

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Sterile Filling & Lyophilization Area_Draxis Pharma

The project consisted in the preparation of a feasibility study, scope, and budget, followed by the supervision of design, construction, and validation for a 6,000 ft2 extension to the sterile core area, and the creation of a new mechanical room for the support equipment and utilities.

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Ultravision Contact Lens Manufacturing Facility

The project consisted in the preparation of the feasibility study, scope and budget for the project, followed by the supervision of design, construction and validation for a 10,000 ft2 Grade C production area for the manufacturing of contact lenses.

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