GMP Compliance Adviser – Corporate Licence


An online publication that covers all aspects of Good Manufacturing Practice (GMP) in one source.

  • multiple users; one user at a time
  • 12-month-subscription

New AI search tool: ChatGMP!

Quick and easy results especially for your GMP questions.


Get Your Free Demo Access Now!

You would like to order a licence for 1 person only? This way please.


Online Corporate Licence

Continually updated

Sofort versandfertig, Lieferzeit ca. 2-5 Werktage

3.480,00 € netto

Bitte beachten: Mit dem Kauf dieses Artikels bestätigen Sie, dass Sie die allgemeinen Lizenzbedingungen gelesen und akzeptiert haben.

X

The GMP Compliance Adviser is an online publication that covers all aspects of Good Manufacturing Practice (GMP) in one source.

In the GMP Compliance Adviser you’ll find:

GMP in Practice
This part contains 21 chapters with GMP expert knowledge to base your decisions upon. It provides practical assistance with checklists, templates and SOP examples.

It is written by 81 authors with hands-on experience directly linked to the industry. The individual chapters describe the different aspects of GMP in a clear language. Technical, organizational and procedural aspects are covered. More than 700 checklists, templates and examples of standard operation procedures taken directly out of the practice help you in understanding the GMP requirements.

GMP Regulations
These 8 chapters cover the most important GMP regulations from Europe and the United States (CFR and FDA), but also PIC/S, ICH, WHO and many more.

Chapter overview

Please click or tap the arrow.

GMP in Practice

Current topics
0.A Nitrosamines
0.B Cannabis
0.C ATMPs
0.D Remote Audits and Inspections
0.E The 2021 PDA/FDA Joint Regulatory Conference: A First-hand Insight
0.F Importation of Medicinal Products
1 Quality Management Systems
2 Personnel
3 Premises
4 Facilities and Equipment
5 Pharmaceutical Water
6 Qualification
7 Process Validation
8 Cleaning Validation
9 Computerised Systems
10 Hygiene
11 Production
12 Sterile Production
13 Packaging
14 Laboratory Controls
15 Documentation
16 Storage and Transportation
17 Outsourced Activities
18 Audits and Supplier Qualification
19 Quality Risk Management
20 Active Pharmaceutical Ingredients
21 Inspections and Drug Safety

GMP Regulations

A Addresses
B National Bodies and Pharmaceutical Associations
C EU Directives and Guidelines
D USA: CFR and FDA Guidelines
E ICH Guidelines
F PIC/S Guidelines
G GMP of other Regions
- Canadian Regulations
- Japanese Regulations
- Chinese Regulations
- Indian Regulations
- Australian Regulations
- Brazilian Regulations
H WHO Guidelines

 

Information

- Update history
- GMP Abbreviations
- GMP Glossary
- Contributors

 


Reach your GMP compliance with the support of the provided knowledge!

Practical features and advantages of the GMP Compliance Adviser

  • comfortable full-text search
  • copy, paste & print
  • bookmarks
  • access via standard browser
  • regular automatic updates
  • email notification about important revisions

Free trial!

The GMP Compliance Adviser is used by more than 10000 professionals in over 50 countries.
Discover for yourself and take a look into this unique, powerful and dependable GMP reference tool:
>>> Get your free demo access now – it ends automatically!


Any questions? Just get in touch with me!

Annette Crawford, crawford@gmp-publishing.com,

+49 (0)7622 66686-74


GMP Compliance through better GMP knowledge – Interview with Thomas Peither
Advantages and Prices

Anonym Am 10.04.2024

Good tool

Service Support has been very very good and always prompt reply. We are very satisfied with the tool

Von Ralf Gengenbach, CEO Gempex GmbH Am 28.04.2020

Detailed Explanations

What I really like about the GMP Compliance Adviser are the regulations on the one hand and the corresponding detailed explanations on the other hand. Furthermore it is ideal that I can always jump to any topic and find the content I need at the time.

Von Teresa Silveira Am 27.05.2019

Note about clients and accounts support

The service support has been very good . All requirements are easily attended: on time and very well communicated.

Congratulations


Greetings,
TSilveira

Bewertungen können anonym erfolgen und werden nach Überprüfung in unserem Webshop veröffentlicht.
Bewertung schreiben

Bitte geben Sie die Zeichenfolge in das nachfolgende Textfeld ein.

Die mit einem * markierten Felder sind Pflichtfelder.

The GMP Compliance Adviser is very easy to use!

You just need internet access with one of these browsers:

  • Explorer (at least: 7)
  • Firefox (at least: 3.6)
  • Chrome (at least: 17)

With the Corporate Licence all employees will have access to the GMP Compliance Adviser Online – regardless of where they are located.

The licence itself is a concurrent license model, which means that one user at a time has access per licence (if you buy two licences – two users at a time).

It works through your company IP addresses (several addresses can be added) – no personalised identification procedure is necessary (user name / password).

For access from outside the IP range, an additional password will be supplemented.

In order to improve our services and make them more interesting for you as a user, we analyse the use of our knowledge portal GMP Compliance Adviser. Further information can be found in our data privacy statement.
 
 

Safety for your daily routine

You are always up to date.

Each update includes either entire new chapters, or some chapters may be partially renewed/supplemented according to the latest GMP guidelines. All regulatory changes are covered, minor or big.

You won’t miss any important changes, because you will be automatically informed about the updates with our e-mail service Insider.

Click here to learn more about content of updates.


Licence agreement

Note for the user: This is a contract between you (“licensee”) and the GMP-Verlag Peither AG (“licenser”). By using the knowledge portal on your computer you agree on all terms and conditions of the present contract. All rights to the knowledge portal are with the GMP-Verlag Peither AG.

This licence agreement applies for the following product:

 

GMP Compliance Adviser

When acquiring a single user licence the following agreement applies:
You obtain the simple, non-exclusive, personal and non-transferable right to use the knowledge portal after receiving the payment and setup of the access. The right of utilisation only applies to you and cannot be transferred to third parties.

You purchase a license with a minimum term of 3 or 12 months.

The three-month license expires automatically after the minimum term without any cancellation required. Twelve-month licenses may be terminated in writing to the expiry of the respective minimum term with a notice period of 1 month to the month-end. Otherwise the license will be extended automatically for another 12 months. The GMP-Verlag Peither AG is particularly entitled to terminate the contract for cause without proper notice if the licensee does not pay in time or provably misuses the knowledge portal.

When acquiring a corporate licence the following agreement applies:
This is a concurrent licence model: it allows multiple users the access, but limits the number of simultaneous users to the number of licenses purchased. After receiving the payment and setup of access you will obtain the right of utilisation.

You purchase a license with a minimum duration of 12 months.

The twelve-month license may be terminated in writing to the expiry of the minimum term with a notice period of 1 month to the month-end. Otherwise the license will be extended automatically for another 12 months. The GMP-Verlag Peither AG is particularly entitled to terminate the contract for cause without proper notice if the licensee does not pay in time or provably misuses the knowledge portal.

The licenser provides the contents of GMP Compliance Adviser in accordance with the terms of a licence for online products to the licensee.

If you have any questions about this present contract or would like to have any information, please contact

GMP-Verlag Peither AG

Karlstrasse 2
79650 Schopfheim (near Basel)

Phone +49 7622 66686-70
Fax +49 7622 66686-77
E-mail: service@gmp-publishing.com
Web: www.gmp-publishing.com

585,00 € netto

625.95 - 7.00

585,00 € netto

625.95 - 7.00

29,90 € netto

31.99 - 7.00

189,00 € netto

202.23 - 7.00

69,90 € netto

74.79 - 7.00

179,00 € netto

191.53 - 7.00

69,90 € netto

74.79 - 7.00

189,00 € netto

202.23 - 7.00

189,00 € netto

202.23 - 7.00

  • An online publication that covers all aspects of Good Manufacturing Practice (GMP) in one...

    585,00 € netto

    625.95 - 7.00

  • Get a quick and comprehensive overview of the complex world of Good Manufacturing Practice (GMP)...

    44,90 € netto

    48.04 - 7.00

  • Das weltweit größte Standardwerk für Qualitätsmanagement in der Pharmaindustrie. Die...

    585,00 € netto

    625.95 - 7.00

  • LOGFILE

    Der Newsletter des GMP-Verlags

    News und aktuelle Trends: Mit dem LOGFILE sind Sie immer up-to-date!

    > Jetzt kostenlos abonnieren!