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CPCSEA Guidelines
A Seminar presented as a part of
I Year M. Pharm I semester Requirement
ACY 2019 – 20
By
M. Kavya Nainita
Regd. No. 19L81S0406
Pharmaceutical Quality Assurance,
Raghavendra Institute of Pharmaceutical
Education & Research (AUTONOMOUS),
Anantapuramu.
18-04-2020 1
CONTENTS
• CPCSEA - Definition
• Goals
• Objective
• Committee members
• Forms
• CPCSEA Annexures
• Animal procurement
• References
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Introduction
• Committee for the Purpose of Control and
Supervision of Experiments on Animals.
• It is statutory committee.
• Established under Section 15 of the prevention
of cruelty to animals act 1960.
• Committee was reconstituted on 17 February,
2016.
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CPCSEA
Definition
Committee for the purpose of control and
supervision of experiments on animals.
• It is statutory body formed by the act of the Indian
Parliament under the Prevention of Cruelty to
Animals Act, 1960.
• The secretariat of CPCSEA has published its
guidelines, to ensure humane and ethical treatment of
animals, while carrying out legitimate scientific
research.
• It was formed in 1964.
• Headquarters is at Ballabhgarh of Faridabad district
in Haryana.
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GOAL
• To promote the humane care of animals used in
research.
• To provide specifications that will enhance animals
well being and quality of research.
• Effective functioning of IAEC.
• To provide guideline for:
Housing, care, breeding and maintenance.
Source of experimental animals
Acceptable experimental procedures for
anaesthesia and euthanasia.
OBJECTIVE
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COMMITTEE MEMBERS
• It is composed of
Members of the scientific
community
Regulatory authorities
Animal activists
The committee has 20 Experts
and 3 Official Members.
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1 Special Secretary / Additional Secretary, In-
charge of Animal Welfare, Government of
India, Ministry of Environment, Forest &
Climate Change, New Delhi
Chairman
2 Joint Secretary (Animal Welfare), Ministry
of Environment, Forest & Climate Change,
New Delhi
Vice Chairman
3 Representative from Drug Controller
General of India (DCGI), New Delhi
Member
4 Representative from Medical Council of
India (MCI), New Delhi
Member
5 Representative from Veterinary Council of
India (VCI), New Delhi
Member
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6 Representative from Pharmacy
Council of India (PCI), New Delhi
Member
7 Representative from University Grants
Commission (UGC), New Delhi
Member
8 Representative from Animal Welfare
Board of India (AWBI), Ballabhgarh
Member
9 Dr. Suresh Pothani, Representative
ICMR, Director In Charge & Scientist
“G” ICMR – National Animal
Resource Facility for Biomedical
Research, Hyderabad
Member
10 Prof. Asmita Gajbhiye, Professor &
Head, Dept of Pharmaceutical
Sciences, Dr. H.S. Gour
Vishwavidyalaya, Sagar
Member
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11 Prof. Alok Dhawan, Director, CSIR –
Indian Institute of Toxicology
Research, Lucknow
Member
12 Dr. Anurag Agrawal, Director, CSIR
– Institute of Genomics & Integrative
Biology, New Delhi
Member
13 Dr. Ram Vishwakarma, Director,
CSIR – Indian Institute of Integrative
Medicine, Jammu
Member
14 Dr. Pardeep Kumar Yadav, Senior
Veterinary Officer, All India Institute
of Medical Science, New Delhi
Member
15 Dr. S.G. Ramachandra, Chief
Research Scientist, Central Animal
Facility, Indian Institute of Science,
Bangalore
Member
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16 Dr. Subeer S. Majumdar, Director,
National Institute of Animal
Biotechnology, Hyderabad
Member
17 Prof. Dr. M. Ramachandra Mohan,
Professor, Dept of Zoology, Bangalore
University
Member
18 Prof. Madan Mohan Chaturvedi,
Professor and Head, Department of
Zoology, University of Delhi, New Delhi
Member
19 Prof. Aditya Kumar, Director, SKS
Institute, Mathura
Member
20 Director/Deputy Secretary (Animal
Welfare) Ministry of Environment,
Forests & Climate Change, New Delhi.
Member
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Forms
Forms Purpose
FORM A [As per rule 5(a)] Application for Registration
with CPCSEA
Form B (per rule 8(a) Submission of Research
Protocol (s) on Large Animals
Form C Record of Animals bred /
acquired
Form D Record of Animals Acquired
and Experiments performed
FORM- E Record of animals sold
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IAEC
• Institutional animal ethical committee.
Definition:
• Body comprising of a group of persons
recognized and registered by the CPCSA.
Function:
• Review and approve all types of protocols for
research involving animal experimentation.
• Obtain the periodic reports on research
development and shall ensure visit to animal
house facility and laboratory.
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Ministry of
Environment
and Forests
(Animal
Welfare)
CPCSEA
IAEC IBSC/IBC
Institutional Bio Safety Committee
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PHARMACEUTICAL QUALITY ASSURANCE
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• Role of CPCSEA is to monitor animal.
Experiments through ethics committees set up
in institutions (IAEC).
• IAEC scrutinize all project proposals for
experimentation on animals.
For small animals- give the final
approval
For large animals-make its
recommendation to SCL
(Sub-Committee on Large
Animals)
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PHARMACEUTICAL QUALITY ASSURANCE
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Qualification
• B. V. Sc
• M.Sc. (Zoology/ Animal Sciences/ Animal
Biotechnology)
• M.Sc. / MTech (Life Sciences, Biological
Sciences/ Biochemistry/ Biotechnology/
Biomedical Engineering) with experience in
animal handling and animal research.
• M. Pharm with experience in animal handling
and animal research.
• MD/ MS with research experience in laboratory
animal handling.
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• Age limit: 65 years.
• Duration: 5 years.
• Inspection report of animal house with
photographs by IAEC members is required to
be sent once in a calendar year.
• If action is required, the facility must provide
within 30 days.
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Veterinary care
•Adequate veterinary care must be provided and
is the responsibility of a veterinarian or a person
who has training or experience in laboratory
animal sciences and medicine.
•Observed regularly for sign of illness, injury or
abnormal behaviour.
•Contagious disease – isolated from healthy
animal.18-04-2020 17
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Surveillance, Diagnosis, Treatment
and Control of disease
(Annexure 1 and 2)
• All animals should be observed for signs of
illness, injury or abnormal behaviour by
animal house staff.
• Unexpected deaths and signs of illness,
distress or other deviations from normal health
conditions in animals.
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Physical Relationship of Animal
Facilities to Laboratories
(Annexure-3)
• Separation of animal facilities from personnel
areas such as offices, conference rooms, and
other laboratories.
• Located away from dust, smoke, noise, wild
rodents, insects and birds.
• Animal rooms should occupy 50-60% of
constructed area.
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Transport of laboratory animals (Annexure – 4)
Mouse Rat Hamster Guinea
pig
Rabbit Cat Dog Monkey
Max.no
Of
animals/
cage
25 25 25 12 2 1 or 2 1 or 2 1
Material
used in
transport
box
Metal
cardboard,
synthetic
material
metal metal Bamboo/
wood/metal
Space/
animal
(cm²)
Minimum
height of
box (cm)
20-25
12
80-
100
14
80-100
12
160-180
15
1000-
1200
30
1400-
1500
40
3000
50
2000-4000
48
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Anaesthesia
(Annexure-5)
• Sedatives, analgesics, anaesthetics should be used to
control pain or distress under experiment.
• Before using anaesthetics the animal is prepared for
anaesthesia by overnight fasting and using pre-
anaesthetics (scopolamine, atropine, diazepam, etc.)
• The animal should remain under veterinary care till it
completely recovers from anaesthesia and
postoperative stress.
Narcosis
Relaxation Analgesia18-04-2020 22
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Euthanasia
(Annexure-6)
• Death without causing anxiety, pain or distress
with minimum time lag phase.
• Done when an animal required to be sacrificed
or termination of an experiment or otherwise
for ethical reasons.
• Tranquilizers have to be administered to larger
species such as monkeys, dogs and cats before
an euthanasia procedure.
18-04-2020 23
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Animal care and Technical
Personnel
(Annexure-7)
• Animal care programs
• On-the-job training
• Trained person in laboratory animal science.
• Protective clothing (face masks, head covers,
aprons, gloves, gumboots, other footwear, etc.)
18-04-2020 24
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Animal Experimentation Involving
Hazardous Agents
(Annexure-8)
• Policies governing experimentation with
hazardous agents.
• Examine the proposal on animal experiments
involving hazardous agents.
• IBSC members are knowledgeable about
hazardous agents are in place in most of the
higher-level education, research institutes and in
many pharmaceutical industries for taking care of
safety issues.
18-04-2020 25
PHARMACEUTICAL QUALITY ASSURANCE
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Animal procurement
• All animals must be acquired lawfully as per
the CPCSEA guidelines.
• A health surveillance program for screening
incoming animals should be carried out to
assess animal quality.
• Each consignment of animals should be
inspected for compliance with procurement
specifications.
18-04-2020 26
PHARMACEUTICAL QUALITY ASSURANCE
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Quarantine
Definition:
• Separation of newly received animals until the
health and possibly the microbial status of
newly received animal have been determine.
• An effective quarantine minimizes the chance
for introduction of pathogens into an
established colony.
• Quarantine period :
 small lab animals- 1 week to 1 month.
 large lab animal – 6weeks.
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Experimental area
• Experiments should be carried out in a
separate area away from the place where they
are housed.
• Separate functional areas for:
 surgical support
Treatment of animals
Post operative and
intensive care
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Stabilization and Separation
• Physiologic, psychological and nutritional
stabilization should be given before their use.
• Separation is needed to prevent interspecies
diseases transmission and to eliminate anxiety
and possible physiological and behavioural
changes due to interspecies conflict.
• To prevent anxiety and behavioural changes.
18-04-2020 29
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Physical facilities
Building materials Durable, moisture – proof, fire
resistant and pest resistant.
corridors Movement of personnel and equipment
Animal room doors Fit properly, no rust
Exterior windows Not recommended
floors Smooth, moisture proof, non absorbent,
skid proof floors
drains Proper drainage, floors should be sloped
Storage areas For feed, bedding, cages
Temperature and humidity Between 18-29 °C and 30-70 %
ventilation Designed with 12-15 air cycles / hour
Power and lighting Fluorescent lights
noise control Noise free environment
Concrete walls are more effective.
18-04-2020 30
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Animal husbandry
Housing system:
Freedom of movement, normal
postural adjustments.
Comfortable environment
Easy access to food and water
Adequate ventilation
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Food and water
Feed should contain Feed should not contain
Moisture Insecticides, hormones, antibiotics,
fumigants or toxicants
Crude fibre, protein, fat Heavy metals
Essential bits, minerals, carbohydrates
•Palatable
•Non-contaminated
•Nutritionally adequate
•Fresh
•Uncontaminated drinking water
18-04-2020 32
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Bedding
• Adsorbent, free from toxic chemicals.
• Should be removed and replaced periodically
with fresh materials.
• Ideal to change the bedding twice in a week.
• Newly delivered pups should be provided
wherever needed. (paper, cotton, etc.)
18-04-2020 33
PHARMACEUTICAL QUALITY ASSURANCE
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Transgenic animals
• Transgenic animals are those animals, into
whose germs line foreign genes have been
engineered.
Used for study of biological functions of
specific genes.
• Knockout animals are those specific genes
have been disrupted leading to loss of function.
Maintained in clean room environment or in
animal isolators.
18-04-2020 34
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Waste disposal
• Removed regularly and frequently.
• Disposed in a safe and sanitary manner.
• Preferred method – Incineration (thermal
treatment – waste materials converts waste into
ash, flue gas and heat).
• Waste cans containing animal tissue, carcasses
and hazardous wastes – leak proof.
• Cold storage might be necessary to prevent
decomposition of biological wastes.
18-04-2020 35
PHARMACEUTICAL QUALITY ASSURANCE
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Emergency, Weekend And Holiday
Care
• If any emergency, institutional security
personnel and fire or police officials should be
able to reach responsible persons for the
animals.
• Emergency veterinary care.
• Posting emergency procedures, names, or
telephone numbers in animals facilities in
security department.
18-04-2020 36
PHARMACEUTICAL QUALITY ASSURANCE
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Multiple surgical procedures on
single animal
• No animal should be used for experimentation
for more than 3 years unless adequate
justification is provided.
18-04-2020 37
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Breeding and Genetics
• The breeding stock must be procured from
CPCSEA registered breeders or suppliers
ensuring that genetic makeup and health status
of animal is known.
18-04-2020 38
PHARMACEUTICAL QUALITY ASSURANCE
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Record keeping
• Staff record- both technical and non-technical.
• Health record of staff animals.
• All SOP’s relevant to the animals.
• Breeding, stock, purchase and sales records.
• Records of experiments conducted with the
number of animals used.
• Death record
• Clinical record of sick animals.
• Training record of sick animals
• Training record of staff involved.
18-04-2020 39
PHARMACEUTICAL QUALITY ASSURANCE
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Standard operating procedures
• Name of author
• Title of sop
• Date of preparation
• Reference of previous SOP
• Objectives
• Detailed information of instruments used in
animal methodology.(Model no., Serial no.)
• Normal value of all parameters
• Hazard identification and risk assessment.
18-04-2020 40
PHARMACEUTICAL QUALITY ASSURANCE
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References
• CPCSEA.nic.in
• Appendix I of the New Zealand “Good Practice
Guide for the Use of Animals in Research, Testing
and Teaching” entitled “Pain: Some Concepts and
Definitions”.
• Derelanko MJ. The toxicologist's pocket
handbook. CRC Press; 2017 Nov 6.
• Olfert ED, Cross BM, McWilliam AA, editors.
Guide to the care and use of experimental
animals. Ottawa: Canadian Council on Animal
Care; 1993.
18-04-2020 41
PHARMACEUTICAL QUALITY ASSURANCE
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I'm so proud !
All of my kids
are going into
research.
18-04-2020 42
PHARMACEUTICAL QUALITY ASSURANCE
RIPER

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Cpcsea ppt

  • 1. CPCSEA Guidelines A Seminar presented as a part of I Year M. Pharm I semester Requirement ACY 2019 – 20 By M. Kavya Nainita Regd. No. 19L81S0406 Pharmaceutical Quality Assurance, Raghavendra Institute of Pharmaceutical Education & Research (AUTONOMOUS), Anantapuramu. 18-04-2020 1
  • 2. CONTENTS • CPCSEA - Definition • Goals • Objective • Committee members • Forms • CPCSEA Annexures • Animal procurement • References 18-04-2020 2 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 3. Introduction • Committee for the Purpose of Control and Supervision of Experiments on Animals. • It is statutory committee. • Established under Section 15 of the prevention of cruelty to animals act 1960. • Committee was reconstituted on 17 February, 2016. 18-04-2020 3 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 4. CPCSEA Definition Committee for the purpose of control and supervision of experiments on animals. • It is statutory body formed by the act of the Indian Parliament under the Prevention of Cruelty to Animals Act, 1960. • The secretariat of CPCSEA has published its guidelines, to ensure humane and ethical treatment of animals, while carrying out legitimate scientific research. • It was formed in 1964. • Headquarters is at Ballabhgarh of Faridabad district in Haryana. 18-04-2020 4 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 5. GOAL • To promote the humane care of animals used in research. • To provide specifications that will enhance animals well being and quality of research. • Effective functioning of IAEC. • To provide guideline for: Housing, care, breeding and maintenance. Source of experimental animals Acceptable experimental procedures for anaesthesia and euthanasia. OBJECTIVE 18-04-2020 5 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 6. COMMITTEE MEMBERS • It is composed of Members of the scientific community Regulatory authorities Animal activists The committee has 20 Experts and 3 Official Members. 18-04-2020 6 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 7. 1 Special Secretary / Additional Secretary, In- charge of Animal Welfare, Government of India, Ministry of Environment, Forest & Climate Change, New Delhi Chairman 2 Joint Secretary (Animal Welfare), Ministry of Environment, Forest & Climate Change, New Delhi Vice Chairman 3 Representative from Drug Controller General of India (DCGI), New Delhi Member 4 Representative from Medical Council of India (MCI), New Delhi Member 5 Representative from Veterinary Council of India (VCI), New Delhi Member 18-04-2020 7 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 8. 6 Representative from Pharmacy Council of India (PCI), New Delhi Member 7 Representative from University Grants Commission (UGC), New Delhi Member 8 Representative from Animal Welfare Board of India (AWBI), Ballabhgarh Member 9 Dr. Suresh Pothani, Representative ICMR, Director In Charge & Scientist “G” ICMR – National Animal Resource Facility for Biomedical Research, Hyderabad Member 10 Prof. Asmita Gajbhiye, Professor & Head, Dept of Pharmaceutical Sciences, Dr. H.S. Gour Vishwavidyalaya, Sagar Member 18-04-2020 8 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 9. 11 Prof. Alok Dhawan, Director, CSIR – Indian Institute of Toxicology Research, Lucknow Member 12 Dr. Anurag Agrawal, Director, CSIR – Institute of Genomics & Integrative Biology, New Delhi Member 13 Dr. Ram Vishwakarma, Director, CSIR – Indian Institute of Integrative Medicine, Jammu Member 14 Dr. Pardeep Kumar Yadav, Senior Veterinary Officer, All India Institute of Medical Science, New Delhi Member 15 Dr. S.G. Ramachandra, Chief Research Scientist, Central Animal Facility, Indian Institute of Science, Bangalore Member 18-04-2020 9 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 10. 16 Dr. Subeer S. Majumdar, Director, National Institute of Animal Biotechnology, Hyderabad Member 17 Prof. Dr. M. Ramachandra Mohan, Professor, Dept of Zoology, Bangalore University Member 18 Prof. Madan Mohan Chaturvedi, Professor and Head, Department of Zoology, University of Delhi, New Delhi Member 19 Prof. Aditya Kumar, Director, SKS Institute, Mathura Member 20 Director/Deputy Secretary (Animal Welfare) Ministry of Environment, Forests & Climate Change, New Delhi. Member 18-04-2020 10 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 11. Forms Forms Purpose FORM A [As per rule 5(a)] Application for Registration with CPCSEA Form B (per rule 8(a) Submission of Research Protocol (s) on Large Animals Form C Record of Animals bred / acquired Form D Record of Animals Acquired and Experiments performed FORM- E Record of animals sold 18-04-2020 11 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 12. IAEC • Institutional animal ethical committee. Definition: • Body comprising of a group of persons recognized and registered by the CPCSA. Function: • Review and approve all types of protocols for research involving animal experimentation. • Obtain the periodic reports on research development and shall ensure visit to animal house facility and laboratory. 18-04-2020 12 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 13. Ministry of Environment and Forests (Animal Welfare) CPCSEA IAEC IBSC/IBC Institutional Bio Safety Committee 18-04-2020 13 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 14. • Role of CPCSEA is to monitor animal. Experiments through ethics committees set up in institutions (IAEC). • IAEC scrutinize all project proposals for experimentation on animals. For small animals- give the final approval For large animals-make its recommendation to SCL (Sub-Committee on Large Animals) 18-04-2020 14 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 15. Qualification • B. V. Sc • M.Sc. (Zoology/ Animal Sciences/ Animal Biotechnology) • M.Sc. / MTech (Life Sciences, Biological Sciences/ Biochemistry/ Biotechnology/ Biomedical Engineering) with experience in animal handling and animal research. • M. Pharm with experience in animal handling and animal research. • MD/ MS with research experience in laboratory animal handling. 18-04-2020 15 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 16. • Age limit: 65 years. • Duration: 5 years. • Inspection report of animal house with photographs by IAEC members is required to be sent once in a calendar year. • If action is required, the facility must provide within 30 days. 18-04-2020 16 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 17. Veterinary care •Adequate veterinary care must be provided and is the responsibility of a veterinarian or a person who has training or experience in laboratory animal sciences and medicine. •Observed regularly for sign of illness, injury or abnormal behaviour. •Contagious disease – isolated from healthy animal.18-04-2020 17 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 18. Surveillance, Diagnosis, Treatment and Control of disease (Annexure 1 and 2) • All animals should be observed for signs of illness, injury or abnormal behaviour by animal house staff. • Unexpected deaths and signs of illness, distress or other deviations from normal health conditions in animals. 18-04-2020 18 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 19. Physical Relationship of Animal Facilities to Laboratories (Annexure-3) • Separation of animal facilities from personnel areas such as offices, conference rooms, and other laboratories. • Located away from dust, smoke, noise, wild rodents, insects and birds. • Animal rooms should occupy 50-60% of constructed area. 18-04-2020 19 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 20. Transport of laboratory animals (Annexure – 4) Mouse Rat Hamster Guinea pig Rabbit Cat Dog Monkey Max.no Of animals/ cage 25 25 25 12 2 1 or 2 1 or 2 1 Material used in transport box Metal cardboard, synthetic material metal metal Bamboo/ wood/metal Space/ animal (cm²) Minimum height of box (cm) 20-25 12 80- 100 14 80-100 12 160-180 15 1000- 1200 30 1400- 1500 40 3000 50 2000-4000 48 18-04-2020 20 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 22. Anaesthesia (Annexure-5) • Sedatives, analgesics, anaesthetics should be used to control pain or distress under experiment. • Before using anaesthetics the animal is prepared for anaesthesia by overnight fasting and using pre- anaesthetics (scopolamine, atropine, diazepam, etc.) • The animal should remain under veterinary care till it completely recovers from anaesthesia and postoperative stress. Narcosis Relaxation Analgesia18-04-2020 22 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 23. Euthanasia (Annexure-6) • Death without causing anxiety, pain or distress with minimum time lag phase. • Done when an animal required to be sacrificed or termination of an experiment or otherwise for ethical reasons. • Tranquilizers have to be administered to larger species such as monkeys, dogs and cats before an euthanasia procedure. 18-04-2020 23 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 24. Animal care and Technical Personnel (Annexure-7) • Animal care programs • On-the-job training • Trained person in laboratory animal science. • Protective clothing (face masks, head covers, aprons, gloves, gumboots, other footwear, etc.) 18-04-2020 24 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 25. Animal Experimentation Involving Hazardous Agents (Annexure-8) • Policies governing experimentation with hazardous agents. • Examine the proposal on animal experiments involving hazardous agents. • IBSC members are knowledgeable about hazardous agents are in place in most of the higher-level education, research institutes and in many pharmaceutical industries for taking care of safety issues. 18-04-2020 25 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 26. Animal procurement • All animals must be acquired lawfully as per the CPCSEA guidelines. • A health surveillance program for screening incoming animals should be carried out to assess animal quality. • Each consignment of animals should be inspected for compliance with procurement specifications. 18-04-2020 26 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 27. Quarantine Definition: • Separation of newly received animals until the health and possibly the microbial status of newly received animal have been determine. • An effective quarantine minimizes the chance for introduction of pathogens into an established colony. • Quarantine period :  small lab animals- 1 week to 1 month.  large lab animal – 6weeks. 18-04-2020 27 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 28. Experimental area • Experiments should be carried out in a separate area away from the place where they are housed. • Separate functional areas for:  surgical support Treatment of animals Post operative and intensive care 18-04-2020 28 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 29. Stabilization and Separation • Physiologic, psychological and nutritional stabilization should be given before their use. • Separation is needed to prevent interspecies diseases transmission and to eliminate anxiety and possible physiological and behavioural changes due to interspecies conflict. • To prevent anxiety and behavioural changes. 18-04-2020 29 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 30. Physical facilities Building materials Durable, moisture – proof, fire resistant and pest resistant. corridors Movement of personnel and equipment Animal room doors Fit properly, no rust Exterior windows Not recommended floors Smooth, moisture proof, non absorbent, skid proof floors drains Proper drainage, floors should be sloped Storage areas For feed, bedding, cages Temperature and humidity Between 18-29 °C and 30-70 % ventilation Designed with 12-15 air cycles / hour Power and lighting Fluorescent lights noise control Noise free environment Concrete walls are more effective. 18-04-2020 30 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 31. Animal husbandry Housing system: Freedom of movement, normal postural adjustments. Comfortable environment Easy access to food and water Adequate ventilation 18-04-2020 31 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 32. Food and water Feed should contain Feed should not contain Moisture Insecticides, hormones, antibiotics, fumigants or toxicants Crude fibre, protein, fat Heavy metals Essential bits, minerals, carbohydrates •Palatable •Non-contaminated •Nutritionally adequate •Fresh •Uncontaminated drinking water 18-04-2020 32 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 33. Bedding • Adsorbent, free from toxic chemicals. • Should be removed and replaced periodically with fresh materials. • Ideal to change the bedding twice in a week. • Newly delivered pups should be provided wherever needed. (paper, cotton, etc.) 18-04-2020 33 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 34. Transgenic animals • Transgenic animals are those animals, into whose germs line foreign genes have been engineered. Used for study of biological functions of specific genes. • Knockout animals are those specific genes have been disrupted leading to loss of function. Maintained in clean room environment or in animal isolators. 18-04-2020 34 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 35. Waste disposal • Removed regularly and frequently. • Disposed in a safe and sanitary manner. • Preferred method – Incineration (thermal treatment – waste materials converts waste into ash, flue gas and heat). • Waste cans containing animal tissue, carcasses and hazardous wastes – leak proof. • Cold storage might be necessary to prevent decomposition of biological wastes. 18-04-2020 35 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 36. Emergency, Weekend And Holiday Care • If any emergency, institutional security personnel and fire or police officials should be able to reach responsible persons for the animals. • Emergency veterinary care. • Posting emergency procedures, names, or telephone numbers in animals facilities in security department. 18-04-2020 36 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 37. Multiple surgical procedures on single animal • No animal should be used for experimentation for more than 3 years unless adequate justification is provided. 18-04-2020 37 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 38. Breeding and Genetics • The breeding stock must be procured from CPCSEA registered breeders or suppliers ensuring that genetic makeup and health status of animal is known. 18-04-2020 38 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 39. Record keeping • Staff record- both technical and non-technical. • Health record of staff animals. • All SOP’s relevant to the animals. • Breeding, stock, purchase and sales records. • Records of experiments conducted with the number of animals used. • Death record • Clinical record of sick animals. • Training record of sick animals • Training record of staff involved. 18-04-2020 39 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 40. Standard operating procedures • Name of author • Title of sop • Date of preparation • Reference of previous SOP • Objectives • Detailed information of instruments used in animal methodology.(Model no., Serial no.) • Normal value of all parameters • Hazard identification and risk assessment. 18-04-2020 40 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 41. References • CPCSEA.nic.in • Appendix I of the New Zealand “Good Practice Guide for the Use of Animals in Research, Testing and Teaching” entitled “Pain: Some Concepts and Definitions”. • Derelanko MJ. The toxicologist's pocket handbook. CRC Press; 2017 Nov 6. • Olfert ED, Cross BM, McWilliam AA, editors. Guide to the care and use of experimental animals. Ottawa: Canadian Council on Animal Care; 1993. 18-04-2020 41 PHARMACEUTICAL QUALITY ASSURANCE RIPER
  • 42. I'm so proud ! All of my kids are going into research. 18-04-2020 42 PHARMACEUTICAL QUALITY ASSURANCE RIPER