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provide a special category of closely specified, scientifically
selected, usually validated cleaning and decontamination agents
and technical support services for critical corporate scientific
and manufacturing activities. Experienced CANI staff are recognized
technical experts with over 20 years experience serving the
entire range of healthcare manufacturing including basic research,
laboratory animal research, pilot and clinical facilities,
bulk compound production and finished products from drugs
to medical devices to personal care products. We help FDA
regulated facilities more effectively utilize purchased chemical
budgets to achieve significant operational savings in time,
labor, utilities, and regulatory costs.
Our
corporate account program and resulting vendor consolidation
can also improve inventory management, order handling expense
and provide tangible budget savings throughout the organization.
Standardizing with CANI can reduce dozens of products and
vendors to a manageable few.
If
some of your facilities have already qualified or validated
cleaning agents from other suppliers, you do not have to be
locked in. In many cases, CANI can provide products so similar
that they meet current specifications and so can be approved
as alternates with simple change control documentation. Extensive
testing or revalidation is not required. Based on prior
experience at numerous FDA regulated facilities, we can probably
offer major cost savings approaching 20% compared to your
current cleaning agents.
These
comprehensive, single source contamination control programs
offered through CANI can provide a consistent long-term partnership
to address the significant competitive challenges facing the
pharmaceutical industry and life science companies. CANI is
uniquely capable of helping all your various facilities address
FDA and EPA compliance issues, workplace productivity and
operating efficiency from the point of discovery to the point
of delivery at a plant and laboratory level as well as the
corporate level.
CANI
teams can handle any or all parts of the corporate cleaning
improvement project from assessment and information gathering,
to analysis and diagnostic, to development and recommendations,
to design, validation and implementation, to the ongoing supply
of quality cleaning agents and consumables.
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