RSS Newsfeed  Your shopping cart.

Search in



ECA Working Groups - Analytical Quality Control




So far the following project list was agreed on:

  • Generation of a harmonised SOP on managing analytical deviations within the laboratory including OOS, OOE and OOT results.

For more information on this project please also see the news section. If you are interested in getting actively involved in this first project, please send an e-mail to or use the contact form on one the following sites.

  • Definition of prerequisites for reduced sampling and reduced testing in the quality control of incoming starting materials (APIs and excipients).
  Next section: News  
 GMP Conferences by Topics
 Quality Assurance
 GMP in Biotechnology
 Regulatory Affairs
 GMP in Pharmaceutical Development
 Quality Control
 Storage, Distribution, Transportation
 Sterile / Aseptic Manufacturing
 Computer Validation
 Technical Operations
 GMP for APIs and Excipients
 Medical Devices