5 EASY FACTS ABOUT PHARMA CONSULTANTS IN INDIA DESCRIBED

5 Easy Facts About pharma consultants in India Described

5 Easy Facts About pharma consultants in India Described

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Kellerman Consulting came towards the rescue for me following working with another competitor who still left me at nighttime. I used to be so relieved to locate a accountable, experienced consulting organization who could assistance a new operator out in creating a full blown HACCP plan - and teach me along just how!

We comprehend the numerous challenges and issues you encounter on the strategy to acquiring GMP compliance from the pharmaceutical, biotechnology, ATMP and clinical device producing industries - and we build realistic, achievable and cost-efficient remedies in your case.

- When report essential on urgent basis to assist the supply, regulatory submissions and so forth., When manufacturing web site can’t accommodate the audit as a result of busy schedule, When vacation restriction; Sponsor could get Advantages by buying our IGAP reports from our report databases, In addition our shoppers only spend a little portion of The prices generally linked to conducting a provider audit.

Zero Defect: Building an item which includes no defects but making certain the quality criteria and decreasing the defects to some volume of zero from the assignments.

Kellerman Consulting held my hand each individual action of just how (and belief me I required it)! Kellerman Consulting got me by means of all of my approvals having an simple to follow HACCP approach that appeased a USDA regional manager.

Christina Sanchez Miller, MPH has over 20 years of management, biologics, high-quality assurance and investigate encounter from the professional medical field. She is a broadcast writer in scientific textbooks, papers and has introduced at several Worldwide conferences.

Design and style assessment can be a nicely-recognized GMP consultancy assistance. By this method prepared or currently designed technological machines and installations are approved on high quality by design requirements, suitability and GMP compliance.

We've finished a lot more than seven hundred+ Vendor/Supplier Qualification audits. Regionally primarily based consultants in broader geography so productive top quality of work without language barrier read more and vacation constraints.

The EY R&D Workbench for Pharma is a singular tech Option for effective challenge preparing administration, workflow and difficulty and query monitoring in the R&D ecosystem.

I couldn’t have requested for a better enterprise that will help us work on our certification. They were helpful, educational, and acquired our method efficiently transformed with clear professionalism.

Kellerman Consulting does a wonderful occupation of persistently meeting clients’ expectations and check here using time to be familiar with the requires in their distinctive client. Their service goes previously mentioned and outside of anticipations.

As your companion, we could negotiate the prospective assessment minefield of regulatory compliance expert services with insight, hindsight, as well as the obvious benefit of our breadth and depth of data and regulatory compliance consulting. We offer the next pharma consulting regulatory affairs companies for pharmaceutical companies.

- 360 diploma audit technique to evaluate the capabilities and high-quality techniques of suppliers and out-sourcing associates

A necessary prerequisite with the successful and sensible software of the standard assurance applications will be the deep information about possibilities and variation.

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