Many corporations choose to seek the services of consultants to deliver business enterprise help products and services to properly get ready for certification audits . Kellerman Consulting will publish & implement foodstuff safety and quality systems which have been tailor-made on your products and approach.
Our crew is composed of a diverse choice of market veterans and experts in offering useful assistance in complying with regulations in the course of your challenge lifecycle. Among our gurus, we’re proud to have several former GMP inspectors and field experts who carry to your desk their intimate familiarity While using the nuances and intricacies of GMP compliance throughout a task lifecycle.
Whether you are ranging from scratch, or else you’d like us to incorporate your current plans, we’ll compose This system you need to get Accredited.
Zero Defect: Creating an item which includes no defects but making sure the standard requirements and decreasing the defects to the degree of zero during the projects.
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Make sure you choose an industry through the dropdown listing We get the job done with ambitious leaders who want to determine get more info the long run, not disguise from it. Together, we reach extraordinary results.
prepare were good. In the course of the audit it gave me self confidence realizing we had all the things in keeping with BRCGS prerequisites.
Regulatory affairs is Regulatory Compliance Associates backbone. We exceed other pharma consulting providers with market gurus expert in complexities on the pharmaceutical and biopharmaceutical industries.
Kellerman Consulting has supported a huge selection of clients nationwide to productively move their regulatory inspections and their GMP and cGMP certification audits.
During your totally free GMP session, you’ll find out what the necessities are for getting Qualified, the website amount of it prices without having hidden costs, how long it requires, and how our procedure performs to assure you go your GMP certification audit on the primary test.
Most FDA GMP consultants should have GMP consulting practical experience which is a vital qualification given that they may have had prospects to operate with lots of providers and in several settings. The significance of operational encounter, however, shouldn't be forgotten.
- Signing up for our IGAP method/ Audit report library is free of charge for suppliers/manufacture. Our skilled and qualified auditor will carry out complete site audit of provider covering massive amount of molecules/merchandise (if not currently performed) with no demand to provider and comprehensive audit report shall be organized.
Regulatory Compliance Associates pharma regulatory consultants will develop an extensive proof guide of documented proof demonstrating the corrective action taken to remediate non-compliant challenges.
Producing IQVIA’s positions on key traits during the pharma and daily life sciences industries, having a give attention to EMEA.