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Pharmaceutical Manufacturing
           Plant


     Rakesh Kumar Sharma




             R.K Sharma        1
Locations and Surroundings
The factory building (s) for manufacture of
drugs shall be so situated and shall have such
measures as to avoid risk of contamination
from external environment including open
sewage, drain, public lavatory or any factory
which produces disagreeable fumes, excessive
shoot, dust, smoke, chemical or biological
emissions


                     R.K Sharma              2
Location
► Premises must be
  located to minimize
  risks of cross-
  contamination; e.g. not
  located next to a
  factory with high
  airborne levels of fungi
  and yeast
► Photograph shows a
  liquid oral
  manufacturing unit
  situated close to a
  factory producing Malt
  preparations
► This has caused high
  degree of microbial
  contamination
                               R.K Sharma   3
Formulation factories may not be located
 wherever the land or plot is available
►Geography – Free from geographical
 disturbances such as earthquakes
►Climate – Free from disturbances such
 as floods




                  R.K Sharma               4
 Adequately provided with working
  space to allow orderly and logical
  placement of equipments, materials,
  and movement of personnel so as to:
  ►avoid  the risk of mix-up between
   different categories of drugs or with RM,
   intermediates and in-process materials.
  ►avoid the possibilities of contamination
   and cross contamination by providing
   suitable mechanism
                   R.K Sharma              5
►Designed   / constructed / maintained to
 prevent entry of insects, pests, birds,
 vermin & rodents.
►Interior surfaces (walls, floors and
 ceilings) shall be smooth and free from
 cracks and permit easy cleaning,
 painting and disinfection



                   R.K Sharma               6
► Airconditioned, wherever prescribed for the
  operations and dosage forms under
  production.
► The production and dispensing areas shall
  be
   well lighted,
   effectively ventilated with air control facilities
   may have proper Air Handling Units (wherever
    applicable) to maintain conditions including
        ►temperature   and wherever necessary humidity as
         defined for relevant product.
► These conditions shall be appropriate to the
  category of drugs and nature of operations.
                            R.K Sharma                      7
► The walls and floors of the areas where
 manufacture of drugs is carried out shall be
 free from cracks and open joints to avoid
 accumulation of dust.
   These shall be
    ►smooth
    ►washable
    ►coved  and
    ►shall permit easy and effective cleaning and
     disinfection.

                        R.K Sharma                  8
► These shall also be suitable to the comforts
 of the personnel working with
   protective clothing,
   products handled,
   operations undertaken within them in relation to
    the external environment
► Theseareas shall be regularly monitored for
 compliance with the required specifications.



                       R.K Sharma                  9
Other Areas
► Personnel   rest areas/cafeterias/changing
 rooms
   away from operating areas
   prevention of cross-contamination
   prevention of operators going outside in work
    clothes
   provision of access control
   prevention of visitors access to operating areas
► Maintenance   service areas
   separated from production areas whenever
    possible            R.K Sharma                     10
Finish of Floors, Walls and Ceilings
► Difficult   but not impossible to get correct
  surfaces
► Smooth, impervious, hard-wearing, easy to
  clean
► Resistant to operations and materials in use
► Windows not opening to the outside
► Avoid sliding doors



                         R.K Sharma               11
►A much better Finish of Floors, Walls
 and Ceilings could look like this. The
 surfaces are epoxy painted and interior
 surfaces are made smooth




                  R.K Sharma               12
Design Principles for logical work
 flow should be considered with
 following aspects
► Process flow
► Material flow




                  R.K Sharma         13
Design Principles for logical work
flow should be considered with following aspects Material flow

                                       People flow

                  QC                   Offices                      Canteen
                                                   Gowning
   Incoming
     goods                                                                    Shipping
                                                                  Corridor
                       Corridor
                            Corridor
    Raw
  Materials                                                                   Finished
                                                                  Packaging
      &                                                Filling                Products
  Packaging Weighing          Processing
                                                                              Storage
   Storage

                       Washing          Machine
                                        Shop
                                                                        Corridor
                Utilities and Services                           Waste Treatment



                                          R.K Sharma                                     14
Manufacturing and Packaging Areas
► Pipe-work    and other fittings placed to avoid
  recesses
► Drain design:
   equipped to prevent backflow
   open channels avoided
► Effective   air handling to suit product
     Temperature
     Humidity
     Air filtration
     Environment monitoring
                        R.K Sharma                  15
Manufacturing and Packaging Areas
► Specifically designed and laid out to avoid
  mix-ups and cross-contamination
    Changing facilities to provide segregated
     access
► Prevention of cross-contamination
► Suitable lighting levels




                     R.K Sharma                  16
In-Process and QC laboratories

► Located
        separate from but near
 manufacturing
   prevention of cross-contamination
   separate biological & microbiological areas
► Designed   for the operations being carried
 out
   suitable storage space

                       R.K Sharma                 17
Design aspects - Tablets
► Lay out for Tablets could be
     ► Room  for Weight checking, Sifting, Milling, Mixing, Granulation
     ► Room for Paste preparation
     ► Room for Drying – FBD and or Tray driers
     ► Room for Equipment Washing
     ► Room for maintenance of clean equipment
     ► Compression cubicles
     ► IPQC area
     ► Coating Area
          Coating solution preparation
          Sugar & Film coating operations, drying (if necessary) - a tray drier
     ► Inspectionarea
     ► Quarantine Area
     ► Packing Area Strip Blister or Bulk

                                   R.K Sharma                                  18
Materials Flow - Tablets
► Receipt of Dispensed RM 
► Sifting  Mixing  Granulation  Wet Milling
   Drying  Milling  Lubrication
► Blend Analysis  Compression 
► Quarantine  QA release  Inspection 
  Primary Packing or
► Coating  Inspection  Primary Packing 
► Secondary Packing

                      R.K Sharma             19
Design aspects -
          Liquid Oral Preparations
► Sugar   Syrup Preparation area
► Area for preparation of solids for suspension
► Compounding and filtration / Homogenization area
► Equipment washing area and area for maintaining
  clean equipment
► Bottle washing area
► Filling area
► Labeling and packing area


                       R.K Sharma                20
Materials Flow - Liquid Oral preparations (Syrups
  and Suspensions)
► Receipt of Dispensed RM 
► Weight Checking 
► Milling (for suspensions)  Sifting (for
  suspensions)
► Syrup Preparation 
► Compounding  Filtration or Homogenizing 
  QC Approval 
► Bottle Washing  Filling & Sealing 
► Checking Packing
                      R.K Sharma              21

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Pharmaceutical manufacturing plant

  • 1. Pharmaceutical Manufacturing Plant Rakesh Kumar Sharma R.K Sharma 1
  • 2. Locations and Surroundings The factory building (s) for manufacture of drugs shall be so situated and shall have such measures as to avoid risk of contamination from external environment including open sewage, drain, public lavatory or any factory which produces disagreeable fumes, excessive shoot, dust, smoke, chemical or biological emissions R.K Sharma 2
  • 3. Location ► Premises must be located to minimize risks of cross- contamination; e.g. not located next to a factory with high airborne levels of fungi and yeast ► Photograph shows a liquid oral manufacturing unit situated close to a factory producing Malt preparations ► This has caused high degree of microbial contamination R.K Sharma 3
  • 4. Formulation factories may not be located wherever the land or plot is available ►Geography – Free from geographical disturbances such as earthquakes ►Climate – Free from disturbances such as floods R.K Sharma 4
  • 5.  Adequately provided with working space to allow orderly and logical placement of equipments, materials, and movement of personnel so as to: ►avoid the risk of mix-up between different categories of drugs or with RM, intermediates and in-process materials. ►avoid the possibilities of contamination and cross contamination by providing suitable mechanism R.K Sharma 5
  • 6. ►Designed / constructed / maintained to prevent entry of insects, pests, birds, vermin & rodents. ►Interior surfaces (walls, floors and ceilings) shall be smooth and free from cracks and permit easy cleaning, painting and disinfection R.K Sharma 6
  • 7. ► Airconditioned, wherever prescribed for the operations and dosage forms under production. ► The production and dispensing areas shall be  well lighted,  effectively ventilated with air control facilities  may have proper Air Handling Units (wherever applicable) to maintain conditions including ►temperature and wherever necessary humidity as defined for relevant product. ► These conditions shall be appropriate to the category of drugs and nature of operations. R.K Sharma 7
  • 8. ► The walls and floors of the areas where manufacture of drugs is carried out shall be free from cracks and open joints to avoid accumulation of dust.  These shall be ►smooth ►washable ►coved and ►shall permit easy and effective cleaning and disinfection. R.K Sharma 8
  • 9. ► These shall also be suitable to the comforts of the personnel working with  protective clothing,  products handled,  operations undertaken within them in relation to the external environment ► Theseareas shall be regularly monitored for compliance with the required specifications. R.K Sharma 9
  • 10. Other Areas ► Personnel rest areas/cafeterias/changing rooms  away from operating areas  prevention of cross-contamination  prevention of operators going outside in work clothes  provision of access control  prevention of visitors access to operating areas ► Maintenance service areas  separated from production areas whenever possible R.K Sharma 10
  • 11. Finish of Floors, Walls and Ceilings ► Difficult but not impossible to get correct surfaces ► Smooth, impervious, hard-wearing, easy to clean ► Resistant to operations and materials in use ► Windows not opening to the outside ► Avoid sliding doors R.K Sharma 11
  • 12. ►A much better Finish of Floors, Walls and Ceilings could look like this. The surfaces are epoxy painted and interior surfaces are made smooth R.K Sharma 12
  • 13. Design Principles for logical work flow should be considered with following aspects ► Process flow ► Material flow R.K Sharma 13
  • 14. Design Principles for logical work flow should be considered with following aspects Material flow People flow QC Offices Canteen Gowning Incoming goods Shipping Corridor Corridor Corridor Raw Materials Finished Packaging & Filling Products Packaging Weighing Processing Storage Storage Washing Machine Shop Corridor Utilities and Services Waste Treatment R.K Sharma 14
  • 15. Manufacturing and Packaging Areas ► Pipe-work and other fittings placed to avoid recesses ► Drain design:  equipped to prevent backflow  open channels avoided ► Effective air handling to suit product  Temperature  Humidity  Air filtration  Environment monitoring R.K Sharma 15
  • 16. Manufacturing and Packaging Areas ► Specifically designed and laid out to avoid mix-ups and cross-contamination  Changing facilities to provide segregated access ► Prevention of cross-contamination ► Suitable lighting levels R.K Sharma 16
  • 17. In-Process and QC laboratories ► Located separate from but near manufacturing  prevention of cross-contamination  separate biological & microbiological areas ► Designed for the operations being carried out  suitable storage space R.K Sharma 17
  • 18. Design aspects - Tablets ► Lay out for Tablets could be ► Room for Weight checking, Sifting, Milling, Mixing, Granulation ► Room for Paste preparation ► Room for Drying – FBD and or Tray driers ► Room for Equipment Washing ► Room for maintenance of clean equipment ► Compression cubicles ► IPQC area ► Coating Area  Coating solution preparation  Sugar & Film coating operations, drying (if necessary) - a tray drier ► Inspectionarea ► Quarantine Area ► Packing Area Strip Blister or Bulk R.K Sharma 18
  • 19. Materials Flow - Tablets ► Receipt of Dispensed RM  ► Sifting  Mixing  Granulation  Wet Milling  Drying  Milling  Lubrication ► Blend Analysis  Compression  ► Quarantine  QA release  Inspection  Primary Packing or ► Coating  Inspection  Primary Packing  ► Secondary Packing R.K Sharma 19
  • 20. Design aspects - Liquid Oral Preparations ► Sugar Syrup Preparation area ► Area for preparation of solids for suspension ► Compounding and filtration / Homogenization area ► Equipment washing area and area for maintaining clean equipment ► Bottle washing area ► Filling area ► Labeling and packing area R.K Sharma 20
  • 21. Materials Flow - Liquid Oral preparations (Syrups and Suspensions) ► Receipt of Dispensed RM  ► Weight Checking  ► Milling (for suspensions)  Sifting (for suspensions) ► Syrup Preparation  ► Compounding  Filtration or Homogenizing  QC Approval  ► Bottle Washing  Filling & Sealing  ► Checking Packing R.K Sharma 21