RT Journal Article
SR Electronic
T1 Validation and Environmental Monitoring of Aseptic Processing
JF PDA Journal of Pharmaceutical Science and Technology
JO PDA J Pharm Sci Technol
FD Parenteral Drug Association (PDA)
SP 272
OP 277
VO 44
IS 5
A1 F.I.P. (International Pharmaceutical Federation)
YR 1990
UL http://journal.pda.org/content/44/5/272.abstract
AB The many different checkpoints concerning the complementary activities of validation and monitoring of aseptically processed pharmaceutical preparations are described. The features are based on the official and current GMP guidelines. These are outlined in practical terms according to the personal experience of the authors and manufacturing specialists who were consulted.