GLP Basics

21CFRPART11
21CFRPART58
ARCHIVES
AUDITREPORT
CALIBRATION
COMMISSIONER
CONTAMINATION
CONTROLARTICLE
DEVIATION
DISQUALIFICATION
FDA
FINALREPORT
GLP
MAINTENANCE
MARKETINGPERMIT
MASTERSCHEDULE
NON-CLINICAL
ORGANIZATIONCHART
PHASEINSPECTION
PROTOCOL
QUALITYASSURANCE
SPECIES
SPECIMEN
SPONSOR
TESTINGFACILITY
TESTSYSTEMS
TRAININGRECORD
WARNINGLETTER

This word search contains basic GLP terms. See if you can unscramble the words and find them all.

Try to find all 28 words on this board.

K N O I T C E P S N I E S A H P N V H U
R L G N C O E R E C N A N E T N I A M X
I O D O D N L O S P E C I M E N U F O N
Q X I I T T C T P L C R V G G Q J R W R
R W Y T I A I O S P O N S O R U G L P E
E R T A M M T C S E V I H C R A A M D A
T B I C R I R O P A V L U O N L U A R W
T R L I E N A L E A T B L I O I D S O C
E H I F P A L I C D E M Z C N T I T C O
L 2 C I G T O X I F S A T A - Y T E E M
G 1 A L N I R W E B T W R L C A R R R M
N C F A I O T X S I S V O I L S E S G I
I F G U T N N D O V Y R P B I S P C N S
N R N Q E S O N B F S O E R N U O H I S
R P I S K F C O E D T H R A I R R E N I
A A T I R H E G L K E G L T C A T D I O
W R S D A H A B P K M R A I A N Q U A N
T T E R M T F M W O S P N O L C W L R E
L 1 T N O I T A I V E D I N S E W E T R
U 1 Q E L N O P C 2 1 C F R P A R T 5 8
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Answer Key for GLP Basics

X
Y
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1# N O I T C E P S N I E S A H P # # # #
2# # # N # O E R E C N A N E T N I A M #
3# # # O # N L O S P E C I M E N # # O #
4# # # I T T C T # # # # # # # Q # R # #
5R # Y T I A I O S P O N S O R U G L P #
6E # T A M M T C S E V I H C R A A M D #
7T # I C R I R O P # # # # # N L U A R #
8T # L I E N A L E A T # # I O I D S O C
9E # I F P A L # C D E # Z C N T I T C O
10L 2 C I G T O # I F S A T A - Y T E E M
11G 1 A L N I R # E # T # R L C A R R R M
12N C F A I O T # S I S # O I L S E S G I
13I F G U T N N # O # Y # P B I S P C N S
14N R N Q E # O N # # S # E R N U O H I S
15R P I S K # C # # # T # R A I R R E N I
16A A T I R H # # # # E # L T C A T D I O
17W R S D A # # # # # M # A I A N # U A N
18# T E R M # # # # # S # N O L C # L R E
19# 1 T N O I T A I V E D I N # E # E T R
20# 1 # # # # # # # 2 1 C F R P A R T 5 8
Word X Y Direction
21CFRPART11  212s
21CFRPART58  1020e
ARCHIVES  166w
AUDITREPORT  176s
CALIBRATION  149s
COMMISSIONER  208s
CONTAMINATION  61s
CONTROLARTICLE  715n
DEVIATION  1219w
DISQUALIFICATION  416n
FDA  1010n
FINALREPORT  1320n
GLP  175e
MAINTENANCE  192w
MARKETINGPERMIT  517n
MASTERSCHEDULE  186s
NON-CLINICAL  157s
ORGANIZATIONCHART  1111sw
PHASEINSPECTION  161w
PROTOCOL  81s
QUALITYASSURANCE  166s
SPECIES  96s
SPECIMEN  93e
SPONSOR  95e
TESTINGFACILITY  319n
TESTSYSTEMS  118s
TRAININGRECORD  1919n
WARNINGLETTER  116n