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Award for the
GMP Compliance Adviser

GMP knowledge that convinces.

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On 7 June 2016 Maas & Peither GMP Publishing has received a

SIPAward in the category
"Best New Success Story" and was awarded with the 3rd place.

The GMP MANUAL (now: GMP Compliance Adviser) impressed the jury with "Safe Drugs through Better GMP Understanding".


KNOWLEDGE IS POWER!

The GMP Compliance Adviser is the most powerful and dependable reference tool in the world.

Indispensable for

  • pharmaceutical manufacturers,
  • suppliers,
  • consultants and
  • engineering companies
that need the most updated information available.

Start right away with
the GMP Compliance Adviser.


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GMP Compliance Adviser

GMP in Practice: 24 chapters written by internationally renowned industry experts.

 

GMP Regulations: 8 chapters with the most important GMP guidelines and regulations.

 

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Updates Forecast & History

2017-06-23

GMP Compliance Adviser Update No. 5/2017 (online version only)

With this GMP Compliance Adviser UPDATE you have direct access to all prime regulatory changes and to our GMP expert interpretations. Here are the new features at a glance:

GMP Regulations

C.10
Compilation of Community Procedures on Inspections and Exchange of Information
C.10.1

Conduct of Inspections of Pharmaceutical Manufacturers or Importers

C.10.2 Outline of a Procedure for Co-ordinating the Verification of the GMP Status of Manufacturers in Third Countries
C.10.3 Guideline on Training and Qualifications of GMP Inspectors
C.10.4 Guidance on the occasions when it is appropriate for competent authorities to conduct inspections at the premises of manufacturers, importers and distributors of active substances and manufacturers or importers of excipients used as starting materials
C.10.5 The Issue and Update of GMP Certificates
C.10.6 A Model for Risk Based Planning for Inspections of Pharmaceutical Manufacturers
C.10.7 Procedure for dealing with serious GMP non-compliance requiring co-ordinated measures to protect public or animal health
C.10.8 Procedure for Dealing with Serious GMP Non-Compliance Information Originating from Third Country Authorities or International Organisations
C.10.9 Guideline on Training and Qualification of Inspectors Performing Inspections of Wholesale Distributors
C.10.10 GDP Inspection Procedure (Medicinal Products for Human Use)
C.10.11 The Issue and Update of GDP Certificates (Medicinal Products for Human Use)

 

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