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.

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

X
Y
1234567891011121314151617181920
1# # # # # # # R E T T E L G N I N R A W
2N O I T C E P S N I E S A H P # D # # #
3O # N E # S P E C I M E N D # R P # O #
4N # O S M E T S Y S T S E T O Q L R # #
5- # I T # # # # # # # V # C # U G # # #
6C # T I M R E P G N I T E K R A M # N #
7L C A N # # # # # A # R # O N L A N O #
8I O C G # # # # T # G # S I # I S O I #
9N N I F D A # I # N # N Z # # T T I T 8
10I T F A # # O # I # O A # # # Y E T A 5
11C R I C # N # N # P T # # # # A R A N T
12A O L I # # I # S I # # # # # S S R I R
13L L A L # A # L O C O T O R P S C B M A
14# A U I R # # N # # # # # # # U H I A P
15# R Q T 2 1 C F R P A R T 1 1 R E L T R
16# T S Y # H # # S E V I H C R A D A N F
17# I I M A I N T E N A N C E # N U C O C
18# C D R R E N O I S S I M M O C L # C 1
19# L T # A U D I T R E P O R T E E # # 2
20# E S P E C I E S F I N A L R E P O R T
Word X Y Direction
21CFRPART11  715e
21CFRPART58  2019n
ARCHIVES  1616w
AUDITREPORT  519e
CALIBRATION  1817n
COMMISSIONER  1618w
CONTAMINATION  1918n
CONTROLARTICLE  27s
DEVIATION  143sw
DISQUALIFICATION  317n
FDA  49e
FINALREPORT  1020e
GLP  175n
MAINTENANCE  417e
MARKETINGPERMIT  166w
MASTERSCHEDULE  176s
NON-CLINICAL  12s
ORGANIZATIONCHART  1111sw
PHASEINSPECTION  152w
PROTOCOL  1513w
QUALITYASSURANCE  166s
SPECIES  320e
SPECIMEN  63e
SPONSOR  912ne
TESTINGFACILITY  42s
TESTSYSTEMS  144w
TRAININGRECORD  415ne
WARNINGLETTER  191w