28 considerations  of  Good  Food  Production  Practice  for  home  industry  that
was issued by The Indonesian National Agency of  Drug and Food Control 2003 and are designed based on the capacity and capability of the jamu
gendong producers by taking into account their financial status.
3.3.2   Developing   Guidelines  For a  Good Jamu  Gendong  Production
Practice  GJGPP  Indonesian  National  Agency  of    Drug  and  Food Control, 2003
Guideline development is based on the observations and laboratory results  that  was  previously  conducted.  Development  was  by  taking  into
considerations  of Good  Food  Production  Practice  for  home  industry  that was issued by The Indonesian National Agency of Drug and Food Control
2003 and the results of evaluation of jamu gendong production process. Other considerations was based on the capacity and capability of the jamu
gendong producers thats practical and easy to follow by considering their financial status.
3.3.3 Implementation  of  Good   Jamu  Gendong  Production  Practice
GJGPP
Guidelines  were  implemented  on  the  producers  that  has participated  since  the  beginning  of  the  study.  This  was  conducted  by
visiting  the  location  of  the  production  and  perform  a  socialization  and training to the producers regarding the guidelines and carry out a carefull
supervision  throughout  processing  to  ensure  the  applicabillity  of  the guidelines  and  identify  the  Critical  Control  Points  in  the  implemented
processing using the CCP decision tree.
3.3.4 Product  and  Facility  Microbiological  Evaluation  Before  and  After
Implementation BAM, 2010
Product  from  the  production  was  taken  to  the  laboratory  for evaluation  of  microbiological  quality  Total  Plate  Count  product,
environmental and bottle, Salmonella sp. and Staphylococcus sp. Analyzes and pH. Product evaluation is conducted before and after implementation to
see  the  improvements  of  the  product  microbiological  parameters.  Products that was evaluated were beras kencur and temulawak extract. Methods that
was used are as follows:
3.3.4.1 Environmental Air Evaluation
Salustiano et al 2003
The  number  of  airborne  microorganisms  of  jamu  gendong processing
areas  of    the  production  site  was  evaluated  by  culture  settling plate
method.  Five  point  in  the  area  were evaluated.  The  numbers  of
aerobic  plate  count  were  determined  using  plate  count  agar PCA
by opening    petri  dishes
containing    15-20  ml  of  culture  media  and  were distributed at the production site and exposed for about
15 to 30 minutes. The  Petri  dishes  were  closed  and  incubated  at
48  ±  2  h  at  35°C.  The
29 colonies  were  counted  using  standard  counting  rules  and  the  results  were
expressed as colonyhrm
2
.
3.3.4.2 Microbial Contamination of Jamu Gendong Bottle
Fifty mL of buffer phosphate was rinsed into the investigated bottle. Serial  dilutions  were  prepared  to  achieve  readable  numbers  of  colonies
according to BAM 2010 in the range of 25-250 colonies. These dilutions generally were 10
-1
up to 10
-6
. Ten mL of  the investigated sample was aseptically transfered to 90
mL  of  diluent  10
-1
,  then  1  mL  from  previous  dilutions  was  aseptically dispensed into the next dilutions.  One  mL of  the last three dilutions was
aseptically dispensed onto duplicate Petri dishes using a pipette and sterile tips.  Fifteen  to  twenty  mL  of  plate  count    agar  which  was  tempered
– heated and kept at 45 ± 1ºC in the liquid state was aseptically poured over
pour-plate method and immediately mixed thoroughly and uniformly by a  circular  and  side-to-side  motion  of  plates  on  flat  level  surface.  After
solidified, the agar plates were inverted and incubate promptly for 48 ± 2 h at 35°C.
∑                    ∑
3.3.4.3 Product Total Plate Count BAM, 2010
Serial  dilutions  were  prepared  according  to  to  achieve  readable numbers  of  colonies  according  to  BAM  2010  in  the  range  of  25-250
colonies. These dilutions generally were 10
-1
up to 10
-7
. Total  plate  count  evaluation  procedures  are  as  stated  in  4.2.  The
colonies  were  counted  using  standard  counting  rules  and  the  results  were expressed as CFUmL. Counts computed should be in the range of 25-250
colonies.
∑ [
where: N = Number of colonies per ml or g of product
∑ C = Sum of all colonies on all plates counted n1 = Number of plates in first dilution counted
n2 = Number of plates in second dilution counted d = Dilution from which the first counts were obtained