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Journal of GXP Compliance

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If not now, then when?(LETTER FROM THE EDITOR)(Brief article)
January 01, 2008

GXP talk: a column for discussion of issues identified by readers of t...
January 01, 2008

GCP challenges for 2008 and beyond.(COMMENTARY)(Good Clinical Practice...
January 01, 2008

Strategy and tactics for pilot implementation in the ADDIE Model.(GMP)
January 01, 2008

"GMP" an evolution in application.(GMP)(Good Manufacturing Practices )
January 01, 2008

Applying a risk approach in the simulation of aseptic filling of vacci...
January 01, 2008

Lean compliance for midsized companies.(GMP)
January 01, 2008

How to prepare for a systems-based inspection--understanding FDA's ris...
January 01, 2008

Good practices in the testing laboratory.(Good Laboratory Practice )
January 01, 2008

Corrective action and preventive action (CAPA) in a laboratory.(GLP)
January 01, 2008

Training and the laboratories.(CLASSIC)
January 01, 2008

Expect more from your Quality Assurance group.(GUEST EDITORIAL)
January 01, 2008

21 CFR Part 11: past, present, future.(Code of Federal Regulations)
October 01, 2007

A guide to blend uniformity.
October 01, 2007

Re-establishing a "culture of compliance".(Current Good X Practice)
October 01, 2007

Developing assessments of trainee proficiency: in the world of trainin...
October 01, 2007

Future state CAPA management-a productivity improvement tool.(Correcti...
October 01, 2007

"No man is an island".(LETTER FROM THE EDITOR)(Editorial)
October 01, 2007

GXP talk: a column for discussion of issues identified by readers of t...
October 01, 2007

The U.S. GMP annexes: additional documents needed for dealing with the...
October 01, 2007

From GMP concepts to systems classification and internal GMP policy.(C...
October 01, 2007

What the future holds.(LETTER FROM THE EDITOR)
July 01, 2007

GXP talk: a column for discussion of issues identified by readers of t...
July 01, 2007

Nutraceuticals and the GMP's.
July 01, 2007

Achieving risk management for FDA compliance using ISO 14971.
July 01, 2007

The main differences between Chinese GMP and the international GMP--IC...
July 01, 2007

Dealing with the unthinkable: procedures for evaluating a potential pr...
July 01, 2007

Process transformation for better IT service delivery in the pharmaceu...
July 01, 2007

Conducting a comprehensive remediation analysis for Part 11 compliance...
July 01, 2007

The 'design' phase of the ADDIE model.(analyze, design, develop, imple...
July 01, 2007