“Kellerman Consulting acted for a trainer for our new QC hire, so we benefited from that plus the successful preparation to the SQF audit. We acquired a ninety eight% around the audit. That ought to discuss for by itself.
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We ensure coherent ideas are associated with growth and industrial aims, aligned with the latest Concepts and rising technologies and regulatory requirements. Built on a job’s really worth of manufacturing and enhancement working experience, we are able to aid you in enabling your products to progress to industry quicker that has a ‘appropriate initially time’ tactic.
As being a passionate college student of industry, Ana is remarkably pushed and committed to bringing value to both of those consumers and their supply chain companions alike.
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Regulatory affairs is Regulatory Compliance Associates spine. We exceed other pharma consulting providers with industry experts experienced in complexities of the pharmaceutical and biopharmaceutical industries.
Kellerman Consulting team members are stored up to date on every task, in order that Anybody of our consultants can certainly step in at any instant to provde the reliability and responsiveness your challenge deserves.
Tetrahedron GMP consultants in India executed SOP to improve the Creation setting up minimize WIP reduction due to scale back get production mismatch, Developing of reduced-Price automation for materials managing.
Experienced dozens of pharmaceutical executives and leaders regarding how to successfully and compliantly use the new digital Instrument to streamline workflows and vital procedures
Assure the caliber of your merchandise by creating a QMS. Valicare's experts will assist you with QM consulting, document planning & implementation.
Our Global Lifetime Sciences sector may help you navigate ahead and obtain sustainable good results in the new wellness-outcomes-driven ecosystem.
What kind of assistance you call for: Our GMP consultants will guide you through the entire process of obtaining your manufacturing authorization plus the corresponding GMP certificate.
The sphere of cell and gene therapy is evolving speedily and dealing with continued technological, regulatory, and commercialization hurdles.
Our authorities put together all significant regulatory submissions and provide substantial high-quality Handle overview for all demo-relevant documentation, for instance: