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.

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

X
Y
1234567891011121314151617181920
1# C # N O I T A C I F I L A U Q S I D #
2# O # # # # # # # # W # # # # # # # # #
3# N # # Y T I L I C A F G N I T S E T #
4# T # T C I L P # # R # D # # # # R E #
5# R # R A M A R # S N # # A 2 # A R S #
6# O C O L R C O # E I # P # 1 H U E T D
7# L O P I E I T # V N L # # C # D N S R
8# A N E B P N O # I G # # N F # I O Y O
9# R T R R G I C # H L # O E R # T I S C
108 T A L A N L O # C E I S M P # R S T E
115 I M A T I C L # R T # E I A # E S E R
12T C I N I T - # # A T # I C R # P I M G
13R L N I O E N # Z # E # C E T # O M S N
14A E A F N K O I # # R # E P 1 # R M # I
15P # T # # R N R O S N O P S 1 # T O # N
16R # I Q U A L I T Y A S S U R A N C E I
17F # O # G M A S T E R S C H E D U L E A
18C # N R # # N O I T A I V E D # # # # R
191 # O P H A S E I N S P E C T I O N # T
202 # # # # # # E C N A N E T N I A M # #
Word X Y Direction
21CFRPART11  157s
21CFRPART58  120n
ARCHIVES  1012n
AUDITREPORT  175s
CALIBRATION  54s
COMMISSIONER  1816n
CONTAMINATION  36s
CONTROLARTICLE  21s
DEVIATION  1518w
DISQUALIFICATION  181w
FDA  123se
FINALREPORT  414n
GLP  118ne
MAINTENANCE  1820w
MARKETINGPERMIT  616n
MASTERSCHEDULE  617e
NON-CLINICAL  715n
ORGANIZATIONCHART  1111ne
PHASEINSPECTION  419e
PROTOCOL  84s
QUALITYASSURANCE  616e
SPECIES  1316n
SPECIMEN  1415n
SPONSOR  1415w
TESTINGFACILITY  193w
TESTSYSTEMS  193s
TRAININGRECORD  2019n
WARNINGLETTER  113s