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Qualification / Validation

Qualification and Validation: Agency Expectations
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pdf download
GMP-Conform Implementation of Annex 15 EU GMP Guide

Excerpt from the GMP Compliance Adviser

NEW ++ NEW ++ NEW
Edition: First edition, 03/2018
57 Pages
ISBN: 978-3-95807-098-1
Delivery: immediately after receipt of payment
Excerpt from the GMP Compliance Adviser

The ultimate prerequisites for GMP-conform pharmaceutical manufacturing are validated processes and qualified equipment! Qualification and validation should prove that the equipment, the procedures and processes used during the manufacture of medicinal products are suitable for their purpose. Previously defined acceptance criteria for the critical quality attributes and process parameters have to be met reproducibly.

This sounds plausible. However, the practical implementation raises many questions. How do you correctly use risk management? By what means can the life cycle concept be realised? How do you organise planning, performance and documentation efficiently and in a GMP-conform manner? And most important of all, what are the expectations of the responsible authorities?

In this report Michael Hiob provides all the answers. It is a “must have” guidance for all those who are involved in qualification and validation

You'll learn in detail about:
  • The Regulatory requirements for qualification and validation
  • Risk management and life cycle concepts
  • Organisation and responsibilities
  • Performance and documentation
Don't fail to order your copy of Qualification and Validation: Agency Expectations!

Technical Requirements

This file is in PDF format!
Filesize: 2,22 MB

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Please note the following procedure guidelines:

If you choose payment by bank transfer:

  • You will receive an advance invoice.
  • After payment is received an email with the download information will be sent.

If you choose payment by credit card:

  • Immediately after the credit card payment you will receive an email with the download information.
  • The invoice will be sent by postal mail as soon as possible.
  • Persons who are responsible for the qualification and validation in the areas of quality management, quality assurance, quality control and production
  • External service providers who support qualification and validation
  • Suppliers of facilities and equipment
  • Persons who are responsible for qualification and validation documents
Hiob, Dr. Michael

After graduating in Pharmacology and receiving a PhD, he worked as Laboratory Manager and GMP Inspector. He is currently responsible for supervising GMP inspections. As a ministerial advisor, he is currently responsible for supervising GMP inspections.

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