|
Journal of GXP Compliance
Click on article title to view & purchase. Articles are sorted by their publication date in reverse chronological order.
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
|