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Water | Slide 1 of 30 January 2006 Water for Pharmaceutical Use Part 3: Inspection of water purification systems Supplementary Training Modules on Good Manufacturing Practice WHO Technical Report Series No 929, 2005. Annex 3

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WHO: Supplementary Training Modules on Good Manufacturing Practice

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Page 1: Water Part3

Water | Slide 1 of 30 January 2006

Water for Pharmaceutical Use

Part 3: Inspection of water

purification systems

Supplementary Training Modules on Good Manufacturing Practice

WHO Technical Report Series No 929, 2005. Annex 3

Page 2: Water Part3

Water | Slide 2 of 30 January 2006

Objectives

To understand:

� The specific requirements when inspecting water systems, including associated documentation

� Water system inspection techniques and approaches

Water for Pharmaceutical Use

Page 3: Water Part3

Water | Slide 3 of 30 January 2006

Prepare an aide-memoire for items to inspect:

Schematic drawing review

Changes to system since installation

Sampling procedure and plan

Specifications, results and trends

Out-of-specification results

Annual system review

Deviations

Water for Pharmaceutical Use

8.

Page 4: Water Part3

Water | Slide 4 of 30 January 2006

Prepare an aide-memoire for items to inspect (2):

Results of system performance monitoring

Out of limit results, failure investigations and alarms recorded

Sanitization procedures and records

Maintenance and repairs logs/records

Instrument calibration and standardization

Qualification and validation including DQ, IQ, OQ, PQ

Requalification when appropriate, etc.

Water for Pharmaceutical Use

8.

Page 5: Water Part3

Water | Slide 5 of 30 January 2006

Where to start:

What is the water to be used for?

– sterile products

– non-sterile products, e.g. oral liquid products, external applications

– solid dosage forms

– washing and rinsing

Start: Document review – site verification – followed by additional document review

Water for Pharmaceutical Use

Page 6: Water Part3

Water | Slide 6 of 30 January 2006

Verification:

Start with document review (e.g. schematic drawing of the system, "water quality manual" if available)

Review change control (in case of changes after qualification and validation)

On site verification (system in accordance with the drawing)

Start source water supply

Pre-treatment and treatment systems

Water for Pharmaceutical Use

Page 7: Water Part3

Water | Slide 7 of 30 January 2006

Documentation should reflect information on:PipelineValves (non-return type)Breather pointsCouplingsPipe slopeVelocitiesSampling pointsDrain points InstrumentationFlow rates

Water for Pharmaceutical Use

Page 8: Water Part3

Water | Slide 8 of 30 January 2006

Documentation should reflect information on (2):

Specification for each system element Standard procedures for use System changesRoutine and non-routine maintenance Investigations and corrective action Validation studiesChemical and microbiological specificationsSampling instructionsTest proceduresResponsible persons Training requirements

Water for Pharmaceutical Use

Page 9: Water Part3

Water | Slide 9 of 30 January 2006

On site review and verification:

Walk through the system, verifying the parts of the system as indicated in the drawing

Review procedures and "on site" records, logs, results

Verify components, sensors, instruments

Inspect the finishing, state, calibration status, labels, pipes, tanks etc as discussed in previous parts of this module

Start with source water supply – follow whole system "loop"

Water for Pharmaceutical Use

Page 10: Water Part3

Water | Slide 10 of 30 January 2006

Well water

� Inspect exposed parts of the well, depth of well

� Check for nearby septic systems, hazardous materials usage (pesticides, fertilizers, etc.)

� Well maintenance

Water for Pharmaceutical Use

Page 11: Water Part3

Water | Slide 11 of 30 January 2006

Raw water storage

� May be required prior to pre-treatment

� Check material of construction

– Concrete, steel are acceptable but check corrosion

– Plastics or plastic linings may leach

� Check cover

– To keep out insects, birds and animals

� Check disinfection practices

Water for Pharmaceutical Use

Page 12: Water Part3

Water | Slide 12 of 30 January 2006

Water treatment system inspection (1)

Checks may include: – dead legs– filters – pipes and fittings– Ionic beds– storage tanks– by-pass lines

Water for Pharmaceutical Use

Page 13: Water Part3

Water | Slide 13 of 30 January 2006

Water treatment system inspection (2)

Checks may include: – pumps

– UV lights

– sample points– reverse osmosis– valves– heat exchangers

– Instruments, controls, gauges, etc.

Water for Pharmaceutical Use

Page 14: Water Part3

Water | Slide 14 of 30 January 2006

Other checks (1)

Stainless steel – PVC and most plastics not recommended

Weld quality

Hygienic couplings

Passivation

Air breaks or “Tundish”

Water for Pharmaceutical Use

Page 15: Water Part3

Water | Slide 15 of 30 January 2006

Other checks (2)

Pipes and pumps

– hygienic couplings

– welded pipes

– hygienic pumps

– hygienic sampling points

– acceptable floor

– no leaks

Water for Pharmaceutical Use

Page 16: Water Part3

Water | Slide 16 of 30 January 2006

Staining on water storage tanks

Corrosion on plates of heat exchangers indicates possible contamination

Other checks (3) Check condition of equipment

Water for Pharmaceutical Use

Page 17: Water Part3

Water | Slide 17 of 30 January 2006

Other checks (4) Maintenance records, maintenance of pump seals and O rings

Water for Pharmaceutical Use

Page 18: Water Part3

Water | Slide 18 of 30 January 2006

Air filters

� Integrity testing, sterilization and replacement frequency

� Check burst discs

Other checks (5)

Water for Pharmaceutical Use

Page 19: Water Part3

Water | Slide 19 of 30 January 2006

� Carefully check by-pass valves and lines

� These sometimes leak or are inadvertently left open

� A blanking piece is better during operation phase

Other checks (6)

Zeolite water softenerexchanges Ca and Mg for Na

Softened waterout to deionizer

By-pass valveBy-pass lines

Water for Pharmaceutical Use

Page 20: Water Part3

Water | Slide 20 of 30 January 2006

Other checks (7)

� Activated carbon bed sanitization

� Temperature-compensated conductivity meters

� Influence of plastic pipe adhesive on TOC

� Non-condensable gases in pure steam

Water for Pharmaceutical Use

Page 21: Water Part3

Water | Slide 21 of 30 January 2006

Other checks (8)

� Polypropylene welding inspection

– checking pin holes

� Retrospective validation of WFI system

� Rouging of WFI storage systems

� Spray ball efficacy

Water for Pharmaceutical Use

Page 22: Water Part3

Water | Slide 22 of 30 January 2006

Other checks (9)

� UV light – monitoring performance and lamp life and

intensity

� Validating ozone dosage

� Specifications for acids, alkalis for DI and sodium chloride

for water softener

� “Normally open” and “normally closed” valves

Water for Pharmaceutical Use

Page 23: Water Part3

Water | Slide 23 of 30 January 2006

Then review additional documentation

Qualification protocols and reports

Change control request (where applicable)

Requalification (where applicable)

QC and microbiology laboratory:

SOP for sampling

Procedures and records

Water for Pharmaceutical Use

Page 24: Water Part3

Water | Slide 24 of 30 January 2006

Sampling (1)

� There must be a sampling procedure

� Sample integrity must be assured

� Sampler training

� Sample point

� Sample size

Water for Pharmaceutical Use

Page 25: Water Part3

Water | Slide 25 of 30 January 2006

Sampling (2)

� Sample container

� Sample label

� Sample transport and storage

� Arrival at the laboratory

� Test method

� When is the test started?

Water for Pharmaceutical Use

Page 26: Water Part3

Water | Slide 26 of 30 January 2006

Testing

� Review method verification

� Chemical testing

� Microbiological testing

– test method

– types of media used

– incubation time and temperature

– objectionable and indicator organisms

– manufacturer must set specifications

Water for Pharmaceutical Use

Page 27: Water Part3

Water | Slide 27 of 30 January 2006

Suggested bacterial limits (CFU /mL)

Sampling location Target 

Alert Action

Raw water 200 300 500

Post multimedia filter 100 300 500

Post softener 100 300 500

Post activated carbon filter 50 300 500

Feed to RO 20 200 500

RO permeate 10 50 100

Points of Use 1 10 100

Water for Pharmaceutical Use

Page 28: Water Part3

Water | Slide 28 of 30 January 2006

Pyrogens and endotoxins

� Any compound injected into mammals which gives rise to fever is a “Pyrogen”

� Endotoxins are pyrogenic, come from Gram negative bacterial cell wall fragments

� Detect endotoxins using a test for lipopolysaccharides (LPS)– rabbit test detects pyrogens– LAL test detects endotoxins

� Ultrafiltration, distillation and RO may remove pyrogens

Water for Pharmaceutical Use

Page 29: Water Part3

Water | Slide 29 of 30 January 2006

I N C O R R E C T W A T E R T R E A T M E N T P L A N T

Group Session

You are given a schematic drawing of a water system to discuss. List any problems and their solutions

Water for Pharmaceutical Use

Page 30: Water Part3

Water | Slide 30 of 30 January 2006

M O D I F I E D W A T E R T R E A T M E N T P L A N T

Group Session

Water for Pharmaceutical Use