“Kellerman Consulting acted being a trainer for our new QC employ, so we benefited from that plus the successful preparing to the SQF audit. We obtained a ninety eight% on the audit. That should discuss for alone.

We are going to assessment your documentation and take a look at your facility, recognize gaps inside your current software and facility functions, and we will let you fill People gaps in order to pass your audit.

As your lover, we are able to negotiate the likely assessment minefield of regulatory compliance solutions with insight, hindsight, as well as very clear benefit of our breadth and depth of information and regulatory compliance consulting. We offer the subsequent pharma consulting regulatory affairs expert services for pharmaceutical providers.

To begin the Regulatory Compliance Associates scoping procedure right now, make sure you enter your info within the blue type down below and click on the submit button at The underside in the webpage.

Our GMP Certification consultants, with their abundant and different experience in organising state on the art production amenities conceptualizing your desire undertaking Based on price range and laws.

“Kellerman Consulting was Qualified, effective, and proceeds to point out their assistance and assistance even after the GMP audit”.

Regulatory affairs is Regulatory Compliance Associates spine. We exceed other pharma consulting corporations with industry professionals expert in complexities from the pharmaceutical and biopharmaceutical industries.

Regulatory affairs is Regulatory Compliance Associates backbone. We exceed other pharma consulting businesses with marketplace specialists professional in complexities on the pharmaceutical and biopharmaceutical industries.

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Through your free of charge GMP more info session, you’ll discover what the requirements are for finding Qualified, how much it prices without concealed service fees, how long it will take, and how our procedure functions to guarantee you move your GMP certification audit on the primary try. 

ADAMAS’s Great Manufacturing Exercise (GMP) experts can function To guage systems at your pharmaceutical, biotechnology, or clinical product Corporation or at your vendor web pages to find out In the event the methods in position are sufficient to meet your manufacturing demands and The existing regulatory specifications.

Combining highly skilled professionals and carefully refined processes with website our entire world-course know-how.

You'll be able to Fee us Using the extensive conception and doc creation in your QMS or have our experts accompany or carry out the processing of personal focal details.

Creating IQVIA’s positions on essential developments within the pharma and lifetime sciences industries, having a deal with EMEA.