Pharmaceutical Cleaning Validation
We understand the only answer to this important question is it must be a science, as it can potentially be a financial life or death matter for a pharmaceutical business. Our answer is based on experience and expertise in the pharmaceutical industry, when helping clients, reduce the time and cost of validation in order to get to market faster at a lower cost.
If validation has already been achieved, our objective is to re-validate and guarantee cleaning can be performed reliably and repeatedly in order to meet and exceed the predetermined levels of cleanliness required for Good Manufacturing Practice &Quality Systems Regulations.
We like to add value through improved productivity. Helping clients avoid costs and save money is motivational. while gaining the 100% confidence of our clients knowing that we do the right things all of the time is inspirational.
Measuring Added Value
We measure, manage and optimise added value using our exclusive Computer Aided Pharmaceutical Management System (CAPMS).
CAPMS is based on our own CAFM suite of technology, currently in use in pharmaceutical, public & private hospitals and nursing homes facilities. Modules within that system are tailored to suit pharmaceutical clients unique needs, with audits, analytics and reports available on-line 24/7/365.