“Kellerman Consulting acted for a coach for our new QC employ the service of, so we benefited from that plus the effective preparing for your SQF audit. We received a 98% within the audit. That ought to speak for by itself.
“We partnered with Kellerman Consulting really early on while in the SQF certification procedure, and by relying on their knowledge and methodical method of collecting, compiling, and Arranging the required documentation, we ended up productive in getting our certification.
Full Employee Engagement: It aims to acquire a society during which Workers care with regards to their work which could come up with a change & consequently improve the efficiency of the company.
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“Kellerman Consulting was Specialist, effective, and continues to show their aid and advice even following the GMP audit”.
Scientific Trials Change the design of scientific study by integrating information, expertise, analytics and engineering from examine design and style as a result of execution to electric power superior decisions.
Providers Products and services EY aids purchasers develop lengthy-phrase worth for all stakeholders. Enabled by knowledge and technological know-how, our companies and alternatives supply have faith in by means of assurance and assistance consumers change, expand and work. Strategy by EY-Parthenon
How you can style and design an air handling system Assembly the requirements of home cleanliness classification and environmental safety?
By using a GMP specialist on board, your organization can target its Main operations though guaranteeing compliance is meticulously taken care of.
We understand the complexities GMP consultants of jogging a everyday living science organization and possess locations of experience which website include each and every side of R&D, operations, regulatory affairs, good quality, and producing.
Get promotional supplies to the existence sciences market place additional swiftly, though lowering risks and slicing charges, Using the EY Good Reviewer.
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This involves one example is, qualification, validation and deviation or modify administration. The Hole analysis is really an active comparison of your proven present state Using the requirements specified by regional or international GMP regulations.