galvmed/ oie stakeholder workshop on harmonisation of ... · veterinary vaccine registration in ......
TRANSCRIPT
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GALVmed / OIE Stakeholder Workshop on harmonisation of registration requirements for
Veterinary Medicinal Products
Johannesburg, 9-11 May 2017
Gillian Cowan
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2. Results of Survey onCurrent Status of
Veterinary Vaccine Registration inSADC Countries
Johannesburg June 2017
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SUMMARY
1.Terminology/ Definitions2.Legislation vs Guidance3.SADC Countries’ responses to questionnaire4.Veterinary Medicines – pharmaceuticals or
biologicals?5.Good Manufacturing Practice6.Batch testing by AU-PANVAC
Slide 2
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1. Glossary of TermsApplicant: Person or company who applies for permission to sell a medicine.Registration: Assessment of data on Safety, Quality and Efficacy of medicine which, if acceptable, leads to approval to place the medicine on the market in that country.Regulatory Authority: Government appointed authority mandated to assess product dossiers submitted by Applicants requesting authorisation to market a medicine.
Veterinary Medicine = Veterinary Pharmaceutical or DrugVeterinary Immunological Product e.g. Vaccine
Slide 3
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Glossary of TermsRegistration dossier: Dossier
including data supporting
SAFETY
QUALITY
EFFICACY
of a medicinal product.
Product Licence / Marketing Authorisation = authorisationawarded to an applicant by a Regulatory Authority to place a medicinal product on the market for a specified or indefinite period of time.
Import permit – permission to import a consignment of a medicine.
Slide 4
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2. General Heirarchy of Law for Human and Veterinary Medicinal Products
Ministerial Ordinance/
Announcement
Ministerial Ordinance/
Announcement
ActAct
Notice / Memorandum/Guideline
Notice / Memorandum/Guideline
Slide 5
Legally Binding?
YES
NO
LEGISLATION
GUIDELINES
REGULATIONS,DIRECTIVES
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3. SADC Countries Questionnaire :Responses received from 12/15 countries
ANGOLA
BOTSWANA
D R CONGO
LESOTHO
MALAWI
NAMIBIA
S. AFRICA
SWAZILAND
SEYCHELLES
TANZANIA
ZAMBIA
ZIMBABWE
Slide 6
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SADC Countries with Regulatory AuthoritiesDoes your country have a Regulatory system for assessing registration dossiers and issuing Marketing Authorisations(MAs)?
Slide 7
YesNoNo response
AngolaDRCMalawiNamibiaS. AfricaSwazilandTanzaniaZambiaZimbabwe
BotswanaLesothoSeychelles*
* Plans to have one
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Same agency for both Human & Veterinary Medicines
“YES”
Angola: will have
Malawi
Namibia
Seychelles
S. Africa (MCC)
Tanzania
Zambia
Zimbabwe
“NO”
DRC
Lesotho, but intend to
S. Africa (DAFF)
Swaziland
Slide 8
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Same Department manages bothVeterinary Pharmaceuticals and Veterinary Vaccines
“Yes”
(Angola)
Malawi
Seychelles
S. Africa (MCC)
Swaziland
Tanzania
Zambia
Zimbabwe
“No” Department specifically for veterinary vaccines:
DRC
Lesotho
S. Africa (DAFF)
Slide 9
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Pharmaceuticals Could be Biological
10
Is there a difference?
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Pharmaceuticals & Biologicals Dossiers
• Molecule/Drug substance
• Pharmacology• Pharmacokinetics• Metabolism• Toxicology in
Lab animals & TS• Residues• Withholding time
• Efficacy –dose / kg bw
Biologicals• Antigen (live or
inactivated)
• Not applicable• Not applicable• Not applicable• Safety in Target
Species• Not applicable*• Zero days
•Efficacy –Immunity/protection
Active ingredient
Safety
Efficacy
*Exceptions, e.g. live zoonotic organisms
11
Pharmaceuticals
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Slide 12
SADC Regional Guidelines domesticated
SADC Guidelines domesticated
yesnono reply
AngolaDRCS.Africa (MCC)S.Africa (DAFF)Zimbabwe
LesothoMalawiNamibiaSeychellesTanzaniaZambia
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Do you allow the use of unlicensed vaccinesin an emergency situation?
YesAngolaDRCNamibia, for FMDSouth Africa
TanzaniaZambiaZimbabwe
NoLesothoSwaziland
Slide 13
Never had a need
MalawiSeychelles
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Do you issue Import Permits and if so who issues them?
Yes Issued by
Angola Inst Vet Services, Min of Ag
DRC DVS/CVO
Malawi Dept Animal Health & Lstock
Namibia, for FMD Reg Authority (NMRC)
Seychelles Min of trade (DoH/DVS)
South Africa MAFF & Min of Health
Swaziland DVS
Tanzania TFDA
Zambia Min of Livestock
Zimbabwe Min of Ag /DVS
No
Lesotho
Slide 14
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Potential for Mutual Recognition of another Country’s Authorisation
Slide 15
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When no suitable veterinary medicines is authorisedis it permissible to use a vaccine that is
Licensed in another African Country ?
Yes
No
No
No
Yes
Yes
No
No
No
Yes
Licensed in a country outside of Africa?
Yes
No
No
No
Yes
Yes
No
No
No
Yes
Slide 16
Licensed for use in another species?YesNoNoNoNoNoNoNoNoNo
AngolaDRCMalawiNamibiaSeychellesS. AfricaSwazilandTanzaniaZambiaZimbabwe
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Do you require veterinary medicines to be licensed in the country of origin prior to your approval?
If from another African countryYesAngolaDRCLesotho MalawiSeychellesSwaziland
Slide 17
NoNamibiaS AfricaTanzaniaZambiaZimbabwe
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Do you require veterinary medicines to be licensed in the country of origin?
If from a non-African countryYesDRCLesothoMalawiSeychellesS. AfricaSwazilandTanzaniaZambiaZimbabwe
NoAngolaNamibia
Slide 18
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If a vaccine is already licensed in an African country do you accept the dossier assessment & MA of the other country?
Yes,
Lesotho
Seychelles
No,
all other countries
Slide 19
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If a vaccine is licensed outside of Africa do you accept the dossier assessment & MA of the other country?
NoAngolaDRCMalawiNamibiaSeychellesS AfricaSwazilandTanzaniaZambiaZimbabwe
YesNone
Slide 20
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Pharmaceuticals Could be Biological
21
Remember there is a difference
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Are the dossier requirements for a veterinary vaccines the same as for a veterinary pharmaceutical?
Yes, the same:DRCMalawiNamibiaS. AfricaSeychelles (pharmacology/PK/tox + safety & efficacy required but no quality or stability data)
ZambiaZimbabwe (but no pharmacology or PK)
No Tanzania: requires data that is specifically appropriate for immunologicals
Slide 22
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How many veterinary vaccines have been registered in your country ?
0 – 10 10 – 50 over 50
2 countries 1 country 6 countries
Do you accept reduced data for vaccines required urgently in the face of a new disease outbreak?
Yes: Namibia, South Africa, Zambia
Slide 23
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Do you expect to see data from challenge studies demonstrating protection?
Country OIE Ph EUR 9CFRDRC ✔
S. Africa ✔ ✔ ✔
Tanzania ✔ ✔ ✔
Zambia ✔ ✔ ✔
Zimbabwe ✔ ✔ ✔
Slide 24
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Average time from receipt of a registration dossier to issuing a Marketing Authorisation
Country Time in monthsDRC 3.5Malawi <6Namibia 12S. Africa 30Swaziland <3.0Tanzania 12Zambia 6 - 9Zimbabwe 19 – 28 Applicants have 60 days to
respond to questions each time
Slide 25
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Are independent Expert Reports required?
No
Yes
N/A or Optional
0 10 20 30 40 50 60
Expert Reports
Slide 26
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Is there a timetable laid down in the regulatory framework from receipt of dossier to issuing MA
Tanzania – Yes: 120 days for fast track; 240 days for normal track
Zimbabwe: Acknowledgement of receipt of an application 1 month, Screening 3 months, Evaluation 3-6 months, Regulatory decision 12 -18 months. Applicants are given 60 days to respond to queries each time. The time-lines listed above do not include the applicant's time taken to respond to queries.
All other countries - No
Slide 27
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Average time from receipt of a registration dossier for a veterinary vaccine to issuing a Marketing Authorisation
Country Total time in months Months for applicant to DRC 3.3 respondMalawi 6Namibia 12S.Africa 30Swaziland 3Tanzania 20Zambia 6-9Zimbabwe 30 2
Slide 28
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Validity of MA before Renewal. Fees for MA/Renewal.
Slide 29
MA Fee
1 year
3 years
5 years
Indefinite/retention fee
Renewal fee
DRC $1000 ✔
Malawi $1000 ✔$500
Namibia $220 ✔ $31S. AfricaDAFF
R 8630 ✔ R 4352
S. AfricaMCC
R30,000 ✔
Tanzania $2000 ✔
Zambia $2,100
Zimbabwe $2000 ✔$300
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Good Manufacturing Practice (GMP)
1. Do you conduct GMP inspections?
2. Do you recognise GMP inspections carried out on veterinary vaccine manufacturers
a) In Africa b) in other countries?
Namibia a) Yes; b) No
All other countries:
a) No b) No
Slide 30
0 50 100
Yes
No
No response
Zimbabwe* does not inspect manufacturers in countries with Stringent Regulatory Authorities (SRAs), e.g. EU, Japan, USA and Australia
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Does your country require batch testing of Veterinary Vaccines by AU-PANVAC?
Slide 31
Yes
No
No responseDRCTanzania
Each batch, beforeplacing on the market?
Batches taken fromDistributors’ fridges?
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Do you have a post-marketing surveillance systemin place?
Slide 32
PharmacovigilenceYesHope to haveNoDRC
MalawiNamibiaS Africa MCC (Human medicines only)TanzaniaAngola
S. Africa DAFFZimbabwe
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Thank you for your patience and attention
picture
Slide 33
Thank you for your attention