Close

Why Risk Quality or 

Compliance Failures?

Finally a single online tool ensures you meet international GMP regulations and pass inspections and audits with utter confidence.

Introducing the GMP Compliance Adviser

Helps you achieve pristine quality at every level, for every process in your pharmaceutical facility

  • Keeps your procedures and facilities ready for inspections at any time 
  • Puts all international regulations at your fingertips—in one online reference 
  • Authoritative procedure templates help you develop field-tested SOPs fast 
  • Enables your quality team to adopt best practices quickly and easily 
  • Covers every aspect of international quality, regulatory and compliance standards in manufacturing, packaging, facilities, documentation, IT, audits and more

With the stakes so high, can you afford

quality or compliance failures?

Few jobs are tougher than staying compliant with exacting, excruciatingly detailed, and rapidly changing worldwide GMP regulations. Not to mention the struggle to enforce uniform quality procedures for every person in your manufacturing and documentation process.


Unfortunately, as you know, the costs of failure are huge. Recalls and production-line shut-downs—even a single day—can cost your company huge sums of money. No wonder quality, compliance and regulatory experts in the pharmaceutical industry feel such pressure to achieve perfection. 


Good news: Your job just got easier—and safer. The GMP Compliance Adviser provides quality, compliance and regulatory managers a single, comprehensive guide to the full range of international requirements they must obey. 


The Adviser explains what you have to do and how to do it.

While you can’t prevent inspections and audits, you needn’t fear them when you have the GMP Compliance Adviser close at hand. Indeed, if you, your employees and your facilities are in full compliance, inspections can be just another day at the office.


The GMP Compliance Adviser gives you a comprehensive, detailed guide to compliance regulations and proven quality practices, as well as wisdom and expert insights into how to prepare for—and pass—inspections and audits. Best of all, this huge library of reference training materials provides resources for every member of your team at every quality and compliance level. 


It’s this simple: Faithfully follow the recommendations in the Adviser, and you’re virtually assured of satisfying inspectors and auditors. 

Keep your procedures and facilities

"inspection-ready" at all times.

Helps you solve virtually any problem, meet any challenge when it comes to quality, regulations and compliance

As a comprehensive compliance and quality assurance tool, no other digital or print resource comes close to the GMP Compliance Adviser. This online reference and training solution will likely be the first—and the last—solution you turn to when you:  

    want to solve CAPA problems or other deviations challenges 

    are looking for quality, compliance or regulatory checklists for your people 

    have regulatory questions or need to find a regulation quickly 

    need to create an accurate, proven SOP 

    are looking for a compliance solution 

    need guidelines for proper documentation 

    want to prepare for upcoming inspections or audits 

    have to correct deficiencies following an inspection or audit 

    need to bring your team up to speed on quality and compliance procedures 


To compare the GMP Compliance Adviser with other web-based services, 

go to Compare.

No other GMP resource answers your quality, compliance and regulation questions so completely, so authoritatively. 

No more searching through multiple websites for the regulations you need: 

GMP Compliance Adviser gives you a single source for all critical EU, FDA, WHO, PIC/S, ICH and HC requirements. You also gain access to comprehensive guidance on these issues - all searchable so you get instant answers:

GMP in Practice

1 Pharmaceutical Quality System (PQS)

2 Personnel

3 Premises

4 Facilities and Equipment

5 Pharmaceutical Water

6 Qualification

7 Process Validation

8 Cleaning Validation

9 Computer System Validation

10 Quality Risk Management

11 Production

12 Sterile Production

13 Packaging

14 Laboratory Controls

15 Documentation

16 Research and Development

17 Contractors and Suppliers

18 Inspections

19 Quality Unit

20 Continual Improvement 

21 Active Pharmaceutical Ingredients 

22 Excipients 

23 Medical Devices 

24 Storage and Transportation 

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

H. WHO Guidelines 

This library of regulations and practices covers the 

entire scope of GMP: You’re prepared for anything

Check out the GMP Compliance Adviser for free!

You want to check the content without registration? 

Check the following small selection of chapters free of charge:

You can also use the full search engine of the GMP Compliance Adviser free of charge. Go to one of the above chapters and search your topic of interest.

Need to see more? Request for more information!

To take a closer look at the GMP Compliance Adviser - put it to the test. 

Just ask us to receive more information or a guided tour. 

Maas & Peither AG – GMP Publishing

Karlstrasse 2

79650 Schopfheim

Germany


Phone +49 7622 666 86-70

eMail: service@gmp-publishing.com

Copyright © 2018 Maas & Peither AG