If you need decontamination but do not have the resources, time or equipment, Vibraclean has your solution. From the smallest enclosure to a large building, our skilled personnel provide the customised treatment you require:
Cleanroom and Laboratory Equipment
Fume Hood | Incubators
Ovens | Centrifuges
Refrigerators & Freezers
Water Bath | Balances & Scales
Chemical Storage Cabinets
Colorimeters | Desiccatorss
…and all other laboratory equipment
With increased air supply, air flow patters with the use of high efficiency filters and room pressurization. The increase air supply brings you the desired air changes per hour for your cleanrooms. We evaluate and provide advise, guidance and service with your critical HVAC infrastructure. Working with stakeholders to develop best plan of action for each project.
Validation of the work with biological and chemical indicators.
Testing and cycle development service is available.
Vibraclean works with trusted partners to ensure the success of your project.
Our core competency lie in the planning, compliance and execution
Closing a license on a facility that operates with chemical or biological hazards can be complicated. Neutralizing these hazards and maintaining regulatory compliance is essential to a successful decommissioning.
Vibraclean works with all stakeholders when planning and executing a decommissioning. Our team of experts work directly with the client, any relevant regulatory agencies, and external consultants to ensure a decommissioning is efficient, compliant, validated, and stress-free.
Equipment inside controlled environments requires decontamination and sterilization for a variety of reasons, whether it be for decommissioning, maintenance, routine cleaning, or due to a hazardous incident, Vibraclean ready to support.
Our team of experts work closely with the relevant regulatory bodies, manufactures, and the client to create a custom tested and validated solution to any equipment contamination issues.
Once a cleanroom is built, the HVAC system is operating and all equipment is installed, a meticulous initial clean is required prior to validation and use. This may require a facility shut down clean.
This important event is performed rapidly, under close control and within the cGMPS
Pre-shutdown activities (planning and scheduling)
Declassification and handover
Reclassification and handover
Post-shutdown activities and completion of the shutdown report
Good record-keeping not only helps you during regulatory inspections (GMP audits), it is mandatory to ensure your documentation practices — and your products — meet industry standards and legal requirements for safety, efficacy and product quality.
We provide industry complaint documentation for the work that we perform. Our SOP documentation meets the requirements of FDA, Health Canada, PHAC, CFIA and other governing agencies.
Vibraclean collaborates with clients and shares SOP documentation to ensure if fits into your organizations templates and best practices.
Our GDP trained staff understand Record-keeping SOPs help manufacturing operations meet their quality standards and risk management standards.
Good documentation practices are also essential for attaining ISO-9001-2015 certification and other industry-specific ISO certifications specific to your industry, e.g. ISO/IEC 17025 (for laboratory testing and calibration standards); ISO/IEC 27001 (for information security management system / ISMS) and ISO 13485:2016 (for medical device manufacturing).
All work is performed under strict NDA agreements.