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

X
Y
1234567891011121314151617181920
1N O I T A C I F I L A U Q S I D # # # #
2O E # # # # # 2 1 C F R P A R T 5 8 # T
3N L O # P H A S E I N S P E C T I O N R
4- C D R L Q # # # # N O I T A I V E D O
5C I R # G U A U D I T R E P O R T # Y P
6L T O S M A R K E T I N G P E R M I T E
7I R C M A L N # # # # # # C 1 # A # I R
8N A E E S I # I # # # # # O 1 P I # L L
9I L R T T T N # Z # # # # N T R N # I A
10C O G S E Y E # # A # # # T R O T # C N
11A R N Y R A M # R R T # # A A T E # A I
12L T I S S S I # O C S I # M P O N # F F
13I N N T C S C # S H E # O I R C A # G D
14B O I S H U E # N I I # # N F O N # N A
15R C A E E R P # O V C # # A C L C # I #
16A # R T D A S # P E E # # T 1 H E # T #
17T # T # U N # # S S P # # I 2 # A # S #
18I # # # L C O M M I S S I O N E R R E #
19O # # # E E # # # # # # # N # # # # T #
20N # R E T T E L G N I N R A W # # # # #
Word X Y Direction
21CFRPART11  1515n
21CFRPART58  82e
ARCHIVES  1010s
AUDITREPORT  75e
CALIBRATION  110s
COMMISSIONER  618e
CONTAMINATION  147s
CONTROLARTICLE  215n
DEVIATION  194w
DISQUALIFICATION  151w
FDA  2012s
FINALREPORT  2012n
GLP  55n
MAINTENANCE  176s
MARKETINGPERMIT  66e
MASTERSCHEDULE  56s
NON-CLINICAL  11s
ORGANIZATIONCHART  1111se
PHASEINSPECTION  53e
PROTOCOL  168s
QUALITYASSURANCE  66s
SPECIES  1118n
SPECIMEN  716n
SPONSOR  917n
TESTINGFACILITY  1919n
TESTSYSTEMS  416n
TRAININGRECORD  317n
WARNINGLETTER  1420w