• gmp-verlag.de
  • GMP Compliance Adviser Login
  • Shopping cart
Shopping cart
Your shopping cart is empty

Show shopping cart...
Stay informed!

You’d like to be regularly informed on the latest developments in Good Manufacturing Practices?


Subscribe to our free GMP Newsletter LOGFILE!


Audit Checklists

Questionnaire for preparing GMP-inspections
€ 219.00
€ 260.61
Der MwSt.-Satz richtet sich nach der Produktart, auf Print-Produkte werden 7% und auf digitale Produkte 19% berechnet. Bei Bundle-Produkten werden beide Steuersätze berücksichtigt. Vor dem endgültigen Auslösen der Bestellung wird die MwSt. bestellspezifisch angezeigt.
More than 650 typical questions related to audits and inspections.

Each question with reference to the current EU GMP Guide Part I/II and the 21 CFRs 210/211/11.

For auditors and manufacturers of drugs and APIs.

NEW: Now modifiable!
Edition: 4th edition, 09/2016
46 Pages
ISBN: 978-3-95807-052-3
Delivery: immediately after receipt of payment
Excerpt from the GMP Compliance Adviser

This convenient document contains in-depth background information about planning for and carrying out audits. With more than 650 questions typically asked during audits or inspections, the questionnaire is arranged by subject-matter. Both parts of the book prepare you in an excellent way for audits (internally and externally) and inspections. The section of the corresponding GMP guidelines is quoted next to each question. This way the background of the question and possible answers can be easily researched in the original guidelines and laws. The questionnaire is a catalogue of typical general questions, which may be asked during an inspection. The questions are referenced to the corresponding GMP regulations. In cases of doubt, the relevant original text can be quickly found.

Now modifiable: Print your checklist out, delete redundant sites or add new sites – use the document in your own convenient way.

These are the main topics of the questionnaire:
I General questions for manufacturers of medicinal products and active pharmaceutical ingredients (API)
II Manufacturing and testing of sterile products
III Trade in active pharmaceutical ingredients (API) and excipients
You can find the complete table of contents in the reading sample.

The GMP Audit Questionnaire works great for both sides - the auditor and the inspected company. It facilitates an efficient preparation for
  • an audit or an inspection to come
  • self-inspections
  • your own GMP audit of suppliers and subcontractors.
The book contains the following chapter from the GMP Compliance Adviser:A perfect workingtool in a compact format with a plenty space to write down your notes.

Click & View: GMP-Audit-Questionnaire

Technical Requirements

This file is in PDF and Microsoft Word format!
Filesize: 2,54 MB

To view PDF files, you need Adobe Reader installed on your computer. If you don't, you will need to download and install it:
>>> Adobe Reader - free download

Are you working with Word 2003 or older? Then you need a converter - for example, the Microsoft Office Compatibility Pack:
>>> Microsoft Converter - free download

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 will be sent with the download information.

If you choose payment by credit card:

  • You will receive immediately after the credit card payment an email with the download information.
  • The invoice will be sent by postal mail as soon as possible.
  • auditors
  • pharmaceutical manufacturers
  • suppliers
Lazar, Max S.

Max Lazar looks back on an outstanding career within the pharmaceutical industry. For more than 35 years he was working with Hoffmann-La Roche. Following his retirement, he established a consulting business specializing in API GMP issues and the training of personnel covering the ICH Q7 Guidance. His more than 40-year career in the pharmaceutical industry includes numerous memberships in professional organisations and chairs of committees.

Oechslein, Dr. Christine

As a freelance GMP trainer, Christine Oechslein provides internal GMP training for pharmaceutical companies, manufacturers of active ingredients and suppliers. She has worked in the pharmaceutical industry for many years. As a speaker for different event organisers and an author, she shares her GMP knowledge in the areas of process validation, GMP training and GMP in development.

Gotter, Dr. Bernhard

Bernhard Gotter took up the position of QA Manager in inspection management at F. Hoffmann-La Roche in 2016. In the previous five years, he had worked at Bayer in quality assurance, auditing, supplier management and project management. During this time, he managed numerous audits, and organised and supported official inspections.

Qualification and Validation: Agency Expectations
GMP Supplier Assessment Questionnaire
GDP Audit Questionnaire