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

X
Y
1234567891011121314151617181920
1# # # A # # # R F I N A L R E P O R T #
2S # D # # T E E # # S P O N S O R # # #
3P F I # # R L T E S T S Y S T E M S O #
4E # S N T O C T # P # C # # # Q # R # #
5C # Q O I P I E # E # A # # # U G # T E
6I # U I M E T L # C # L # # # A P T R L
7E # A T R R R G P I # I # # N L H E A U
8S # L A E T A N R M # B # I O I A S I D
9# E I N P I L I O E # R Z # N T S T N E
108 C F I G D O N T N # A N G - Y E I I H
115 N I M N U R R O # T T O L C A I N N C
12T A C A I A T A C I # I I P L S N G G S
13R N A T T # N W O # # O T # I S S F R R
14A E T N E # O N L # # N A # N U P A E E
15P T I O K # C # # # # # I # I R E C C T
16R N O C R H # # # # # # V # C A C I O S
17F I N # A R C H I V E S E # A N T L R A
18C A # R M # # # # # # # D # L C I I D M
191 M T C O M M I S S I O N E R E O T # #
202 # # # 1 1 T R A P R F C 1 2 # N Y # #
Word X Y Direction
21CFRPART11  1320w
21CFRPART58  120n
ARCHIVES  517e
AUDITREPORT  612n
CALIBRATION  124s
COMMISSIONER  419e
CONTAMINATION  416n
CONTROLARTICLE  715n
DEVIATION  1318n
DISQUALIFICATION  31s
FDA  23ne
FINALREPORT  91e
GLP  1410s
MAINTENANCE  219n
MARKETINGPERMIT  517n
MASTERSCHEDULE  2018n
NON-CLINICAL  157s
ORGANIZATIONCHART  1111sw
PHASEINSPECTION  176s
PROTOCOL  97s
QUALITYASSURANCE  166s
SPECIES  12s
SPECIMEN  103s
SPONSOR  112e
TESTINGFACILITY  186s
TESTSYSTEMS  83e
TRAININGRECORD  195s
WARNINGLETTER  812n