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

X
Y
1234567891011121314151617181920
1# # # E L C I T R A L O R T N O C # # #
2# # # # F I N A L R E P O R T # # # # P
3# # O # P H A S E I N S P E C T I O N R
4# # # R L Q C A L I B R A T I O N # # O
5C # # # G U D E V I A T I O N # # # Y T
6O # # # M A R K E T I N G P E R M I T O
7N # # D A L N O N - C L I N I C A L I C
8T # # R S I # I # S P E C I M E N # L O
9A 8 E O T T # # Z R O S N O P S # # I L
10M 5 C C E Y # # # A R C H I V E S # C #
11I T N E R A # R E T T E L G N I N R A W
12N R A R S S # # # # # I # # # # # # F #
13A A N G C S P E C I E S O # # # # D G #
14T P E N H U # # # # # # # N # # A # N #
15I R T I E R 1 1 T R A P R F C 1 2 # I #
16O F N N D A # # # # # # # # # H # # T #
17N C I I U N T R O P E R T I D U A # S #
18# 1 A A L C O M M I S S I O N E R R E #
19# 2 M R E E # # S M E T S Y S T S E T #
20N O I T A C I F I L A U Q S I D # # # #
Word X Y Direction
21CFRPART11  1515w
21CFRPART58  219n
ARCHIVES  1010e
AUDITREPORT  1717w
CALIBRATION  74e
COMMISSIONER  618e
CONTAMINATION  15s
CONTROLARTICLE  171w
DEVIATION  75e
DISQUALIFICATION  1520w
FDA  1912sw
FINALREPORT  52e
GLP  55n
MAINTENANCE  319n
MARKETINGPERMIT  66e
MASTERSCHEDULE  56s
NON-CLINICAL  77e
ORGANIZATIONCHART  1111se
PHASEINSPECTION  53e
PROTOCOL  202s
QUALITYASSURANCE  66s
SPECIES  613e
SPECIMEN  108e
SPONSOR  169w
TESTINGFACILITY  1919n
TESTSYSTEMS  1919w
TRAININGRECORD  420n
WARNINGLETTER  1911w