Whether you’re in the solution planning, advancement or pharmaceutical lifecycle administration phase or require a remediation approach for just a compliance crisis, Regulatory Compliance Associates will guide you thru each and every pharmaceutical consulting step from the regulatory method.
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We help thousands of corporations, including 17 of the best twenty five global pharmaceutical, biotech, and professional medical gadget organizations, link Together with the specialists they want in the ideal workforce model.
The founding partners, whose personal biodata are given on the web site separately, have a robust determination to Integrity, High-quality and Excellence and get the job done with their shoppers to accomplish the consumer’s targets with complete compliance and rigid adherence to the highest moral expectations inside of a time bound style. We Dwell upto our stated motto "EXPERIENCE, EXPERTISE, EXCELLENCE" in all our consulting engagements.
Kellerman Consulting held my hand each move of the best way (and trust me I essential it)! Kellerman Consulting got me by means of all of my approvals with the very easy to adhere to HACCP plan that appeased a USDA regional manager.
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approach were being terrific. In the course of the audit it gave me self esteem understanding we experienced everything according to BRCGS prerequisites.
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- We ensure that your plant web page fulfills your business objectives although currently being entirely compliant with the newest Great Manufacturing Apply rules and benchmarks.
ADAMAS’s Good Producing Exercise (GMP) authorities can work To judge techniques at your pharmaceutical, biotechnology, or health-related gadget Firm or at your vendor web pages to determine In the event the devices in position are adequate to fulfill your production wants and The present regulatory criteria.
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Acquiring IQVIA’s positions on critical developments inside the pharma and lifestyle sciences industries, which has a target EMEA.
We could offer GMP expert services for unique market options on your issues in addition to in depth packages that address all GMP specifications arising from the context of pharmaceutical manufacturing routines.