SELF INSPECTION CHECKLIST FOR DPI (DRY POEDWE INJECTION)

SELF INSPECTION CHECKLIST FOR DPI (DRY POEDWE INJECTION)

CHANGE ROOM:

  • General Area cleanliness
  • Entry /Exit procedure & Pictorial diagram

GENERAL AREA:

  • General cleanliness
  • Area differential pressure records
  • Equipment status
  • Labeling status
  • Use of protective equipment’s (e.g. Hand gloves, nose masks etc.)
  • Machine uses and clean log record
  • Temperature and relative humidity record of the area
  • Status of batch record of the product being processed
  • Identification of utility services
  • How the facility for Injection designed and constructed to prevent cross contamination and mix-ups.
  • Whether the manufacturing area have entrance through double air lock facility.
  • Whether in the manufacturing area walls, floors and ceiling are impervious, non-shedding, non-cracking, coved at all junctions.
  • Whether the doors and windows and light fixtures are flushed, made up of non fiber shedding material.
  • Whether fly catcher and/or air curtain has been provided at strategic suitable points.
  • Whether the drains are provided with traps to prevent back flow.
  • How drains are maintained.
  • Whether the production area is cleaned and sanitized at the end of every production process.  If yes, whether records maintained.
  • (How the area is sanitized.
  • How sanitization procedures controlled).
  • What is the Sanitizing Agent for cleaning
  • What is the material of construction of tanks, containers, Pipe work and pumps?
  • How tanks, pipe works, and other containers sanitized.
  • Whether the pipelines and services have any dust lodging surface.
  • Whether microbial monitoring of the area is carried out.
  • Whether use of glass containers is restricted. If used which type of glass container used
  • Whether furniture’s are of stainless steel and are capable of cleaned effectively.
  • Decartoning Procedure
  • How sterilize vials & rubber Plug
  • What is the sterilizing agent of Flip off Seal
  • Sterilization record of Vials, Flip off Seal & Rubber Plug
  • Temperature record of DHS & Autoclave
  • Cleaning procedure of garments used in manufacturing
  • Which type of rubber stopper used for lyophilized product
  • Whether cleaning of vials, seals, rubber plug etc. are carried out by suitable machine/devices equipped with high pressure air, water.

Purified Water/Water for Injection:

  • Whether the Microbial quality of purified water/ Water for Injection is monitored routinely.
  • (What is the in house limit of CFU / ml of purified water & Water for Injection).
  • Whether water is tested for freedom from Pathogen on daily basis.  If not what is the schedule.
  • Whether the unit has written procedure for operation and maintenance of purified water/Water for Injection system.  (Specify the method).
  • Weather Water for injection stored in steam jacketed stainless steel container

Manufacturing:

  • Cleaning of Aseptic Area
  • Weather UV light available in aseptic dress cabinet
  • What types of clothing’s are worn by personnel in manufacturing area?
  • Whether the tanks have clean in place facility. If not how tanks are cleaned to prevent accumulation of residual microbial growth and cross-contamination.
  • Whether materials like gunny bags or wooden pallets are allowed in manufacturing areas.
  • Whether separate manufacturing area has been provided,`
  • Specify the room temperature requirement in the manufacturing area.
  • Cleaning of Membrane Holder
  • Rinse test record for manufacturing.
  • Rinse test record for filling m/c.
  • Working of LAF
  • Nitrogen purging during filling
  • Weather filter sterilized periodically
  • Solution filtered through
  • Integrity of filter verified/confirmed during manufacturing
  • Log book status for all machines.
  • Visual inspection checking person rotation frequency.
  • Eye test report of visual inspection checking person.
  • Cleaning of Filter

VIAL LABELLING AND PACKING AREA

  • General cleanliness of corridor
  • Equipment status
  • Labeling status
  • Arrangement of primary packaging materials
  • Arrangement of secondary packaging materials
  • Line clearance procedure
  • Identification of utility services
  • Labeling status
  • Status of batch record of the product being packed
  • Scrap disposal procedure

 

 

 

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