At Aport, effective laboratory relocation regulatory adherence is the cornerstone of every project we undertake.
We understand that relocating a laboratory involves navigating a complex landscape of regulatory requirements.
This is critical to maintaining the integrity and safety of ongoing research and manufacturing operations.
Our team at Aport is equipped with extensive knowledge. We understand the intricacies of regulatory compliance throughout the life science industry.
This expertise allows our clients to trust us to plan and execute all aspects of laboratory relocations effectively.
At Aport, we recognise that a knowledgeable team is essential for successful laboratory relocation.
We have invested in an extensive in-house training facility where our staff learn the principles of regulatory compliance.
This enables our teams to grasp the complexities of lab compliance effectively. Our crews are able to practice and perfect their handling techniques and protocols.
We have dedicated full-time trainers and compliance managers on board. This ensures that all staff undergo comprehensive training and that our relocation crews participate in regular ongoing education.
Our training covers the essentials of working in compliant laboratory environments. We focus on adhering to the regulatory procedures and standard operating protocols (SOPs) that govern the life sciences sector.
Our commitment to compliance extends to the handling of dangerous goods and hazardous materials.
Aport employs full-time Dangerous Goods Safety Advisors (DGSAs) who provide specialist support on relevant jobs.
Our dedicated compliance team collaborates closely with clients on various projects to minimise risk. We also work to ensure adherence to regulations related to the transportation and handling of dangerous goods.
During laboratory relocations, it’s vital to consider the specifics of pre- and post-move Installation Qualification (IQ) and Operational Qualification (OQ) procedures.
At Aport, our comprehensive approach ensures that full awareness is given to these procedures. Any necessary requirements are then integrated into our relocation plans. We also operate with an awareness of the highest standards of GxP compliance.
To bolster our regulatory adherence, Aport utilises audit-based tracking systems for every single laboratory relocation.
This system allows us to document processes meticulously and ensure that all regulatory requirements are met during the move.
We provide validation data to support our clients’ submissions to agencies such as the Food and Drug Administration (FDA) or the European Medicines Agency (EMA) when necessary.
This level of detailed oversight ensures that our clients feel confident in the success of their lab relocation projects.
They know that regulatory compliance is thoroughly documented and validated at each stage.
In the ever changing landscape of the life science industry, regulatory adherence can be a daunting challenge.
Aport is ready to help you navigate this complexity with expertise, diligence and unwavering commitment to your research goals.
Whether you’re considering relocating a laboratory or conducting ongoing research, we are here to assist you every step of the way.
Trust Aport for a successful laboratory relocation, where regulatory ist a fundamental principle of each project we undertake.
Our knowledge, training and specialised support ensure that your laboratory move is seamless, safe and in compliance with all relevant regulations.
Partner with us for your next lab relocation project and experience unparalleled service that puts your safety and success at the forefront.
Contact Aport Global today to discuss your cleanroom relocation needs. Ee can ensure a successful relocation that meets the demands of your industry.
