X hits on this document

Powerpoint document

IV Pan American Conference on Drug Regulatory Harmonization Dominican Republic March 2 – 4, ... - page 14 / 15

24 views

0 shares

0 downloads

0 comments

14 / 15

Chapter 12: Quality Control

Main Aspects

Sampling method and personnel approved by QC department

Qualification and validated  of test methods

Records, manually and/or by recording instruments

Product assessment include review and evaluation of production documentation

Failure investigations for all deviations

Ingredients comply with the marketing authorization

Ingredients are of the required purity in proper containers and correctly labelled

Document info
Document views24
Page views24
Page last viewedSat Oct 29 00:33:44 UTC 2016
Pages15
Paragraphs181
Words965

Comments