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.

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

X
Y
1234567891011121314151617181920
1N # R # # # # 2 1 C F R P A R T 1 1 # #
2O # # E # T R A I N I N G R E C O R D D
3I # T # T M A I N T E N A N C E E C # I
4T # E R # T # # # E # # P # T C L O # S
5C C S # A # E # S # M R # R # N U N C Q
6E O T # R H # L # P O I O # O A D T O U
7P N I R C # C # G T E P C I # R E A M A
8S T N O H # # N O N E C T E # U H M M L
9N R G S I # # C O R I A I # P S C I I I
10I O F N V # O # L I R N # E # S S N S F
11E L A O E L # A # B T # R # S A R A S I
12S A C P S # N # I # # A # A # Y E T I C
13A R I S # I # L # # # # Z # W T T I O A
14H T L # F D A # # # # # # I # I S O N T
15P I I L A C I N I L C - N O N L A N E I
16# C T I M R E P G N I T E K R A M # R O
17# L Y # S M E T S Y S T S E T U G # # N
18# E # # N O I T A I V E D # # Q L R # #
19# # # # # A U D I T R E P O R T P # O #
20# # # # # 8 5 T R A P R F C 1 2 # # # #
Word X Y Direction
21CFRPART11  101e
21CFRPART58  1620w
ARCHIVES  55s
AUDITREPORT  619e
CALIBRATION  615ne
COMMISSIONER  195s
CONTAMINATION  183s
CONTROLARTICLE  25s
DEVIATION  1318w
DISQUALIFICATION  203s
FDA  514e
FINALREPORT  514ne
GLP  1717s
MAINTENANCE  63e
MARKETINGPERMIT  1616w
MASTERSCHEDULE  1716n
NON-CLINICAL  1515w
ORGANIZATIONCHART  1111nw
PHASEINSPECTION  115n
PROTOCOL  134sw
QUALITYASSURANCE  1616n
SPECIES  95se
SPECIMEN  1610nw
SPONSOR  413n
TESTINGFACILITY  33s
TESTSYSTEMS  1517w
TRAININGRECORD  62e
WARNINGLETTER  1412nw