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Introductory Validation and the Cleanroom

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Title: Introductory Validation and the Cleanroom


1
Introductory Validation and the Cleanroom
2
What we see
  • FDA regulations require Documentation
  • These regulations do not provide Guidelines on
    how specifically to product the documentation
  • It is left up to the specific companies to
    design their own documentation system.
  • This includes the process of validation

3
Validation and Qualification
  • Validation contains premises from which a
    conclusion can be logically derived
  • Qualification is a condition or circumstance that
    must be met or complied with

4
Can anyone give examples of validation?
5
Validation organization
  • As a department validation should cover
  • Process
  • Equipment
  • Facilities
  • Computer
  • Cleaning

6
Steps in developing Validation are
7
  • Setup a validation dep.
  • Write a validation plan
  • Write policies, sops and admin procedures
  • Establish change control board
  • Establish document reviewers and approvers
  • Establish document distribution
  • Identify equipment to validate and make a list
  • Assign protocols to all functions
  • Validate most critical equipment first

8
  • Assign equipment numbers
  • Assign protocol numbers
  • Assign change control numbers
  • Change protocols
  • Perform commissioning at the original equipment
    manufacturer
  • Write and execute qualification protocols
  • Deficiencies
  • Deviations
  • Addendums
  • Archiving
  • Requalifiction
  • Internal audits
  • FDA audits

9
Qualification Testing
  • Written qualification protocols are prepared that
    specify the tests to be conducted and the data to
    be collected.
  • Observations are documented.

10
What needs to be tested?
  • Almost everything needs to be tested
  • How does one know?
  • Observe the equipment in operation
  • Major components are typical.

11
What level of testing is required
  • A standard for equipment testing has not been
    made in the pharmaceutical industry
  • Object is to gain confidence that the equipment
    is operating under a state of control. Some
    include
  • Minimum/maximum operating ranges
  • Worst case

12
How much testing is Enough?
  • The number of repetitions of a process step
    during qualification should be based on
    statistical significance.
  • Conventional wisdom
  • Once is chance
  • Twice is nice
  • Three times is validation
  • Sorry but we need to use Statistics.

13
The Cleanroom
  • A room that is clean

14
ISO standard 14644-1
  • A room in which the concentration of airborne
    particles is controlled, and which is constructed
    and used in a manner to minimize the
    introduction, generation, and retention of
    particles inside the room and in which other
    relevant parameters, e.g. temperature, humidity,
    and pressure, are controlled as necessary.

15
Who uses clean rooms
  • Electronics
  • Semiconductor
  • Optics
  • Biotechnology
  • Pharmacy
  • Medical Devices
  • Food and Drink

16
2 major types of cleanrooms
  • Turbulently ventilated room
  • (diffuses)
  • 20 changes per hr min
  • Unidirectional flow
  • Air sweeps across the room (80ft/min)
  • Both have clean air on top, moving to the bottom.

17
Particles
  • Human Hair (100um)
  • Visible particle (50um)
  • E. coli (A bacteria) 1um
  • Particles we typically measure 0.5um

18
Some Numbers of ISO classes limits (particles/m3
of air)
  • Class 1 10
  • Class 2 100
  • Class 3 1000
  • Class 4 10,000
  • Class 5 100,000

19
Also limits on microbe contam
Grade Air sample Settle plates
A lt1 lt1
B 10 5
C 100 50
D 200 50
20
Some Cleanroom Disciplines
  • A walking person generates 1,000,000 particles
    permin (0.5um)
  • Some conditions will preclude work in a cleanroom
  • Skin conditions (dermatitis)
  • Respiratory conditions
  • Microfloura
  • Allergies

21
Other Conditions
  • Good personal hygiene
  • Cosmetics
  • Jewelery
  • Smokers particles and out gassing

22
Control of air transfer
  • Enter and exit through change areas
  • Do not leave doors open
  • Open and close doors quickly
  • Doors usually open inward in production
    facilities
  • Respect the airlocks

23
Behavior
  • Sitting 100k, moving 1milK, walking 5milk
  • Positioning so do not drip on product
  • Use no touch techniques
  • Do not support materials on body
  • Do not talk over product

24
Entry and Exit of Personnel
  • Hygiene
  • Cloths, makeup and jewlery
  • Wash before and after
  • Check yourself and check others
  • Are you protecting product or yourself.
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