We have around thirty a long time of experience acquiring a breadth of pharmaceutical formulations across A selection of indications. Get in touch
Food items manufacturers will have to satisfy hygiene and GMP regulations to make certain item basic safety. GMP serves as a Basis for higher safety management units like HACCP and ISO 22000.
Produce and disseminate proof that solutions essential scientific, regulatory and business questions, enabling you to definitely generate smarter conclusions and meet your stakeholder needs with self-confidence.
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Our committed venture administration group will work intently using your leadership staff to ascertain and keep track of venture milestones, plan actions, information sources, and report on results.
Commissioning, Qualification & Validation We operate with our purchasers to establish scalable resource programs to aid validation initiatives all through the task lifecycle. Whether it's drafting protocols to execution and compilation of knowledge packs, our sources have you included.
Our complete-time GMP consultants answer straight away to all customer queries, which demonstrates one among our Main values.
Kellerman Consulting’s GMP consultants give a published high quality & food items safety manual that is definitely personalized in your solution, system and operation. We provide high quality consulting and meals safety teaching In line with latest FDA regulatory demands and personalized for the GMP certification scheme that you'll be wishing for getting Qualified from.
GMP serves as being a prerequisite for HACCP, and whilst GMP establishes critical production techniques, HACCP signifies a far more Highly developed and detailed food stuff safety method
Law firms searching for check here pharmaceutical consulting firm knowledge inside the remediation of warning letters, consent decrees, 483’s or import bans
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We also support pharmaceutical firms in check here Developing Pharmaceutical Solutions across dosage forms at an accredited formulation improvement laboratory, in line with EU / US reference products. Post development, the products technological innovation is often transferred to your proposed manufacturing location.