1 consensus standards oivd workshop april 22-23, 2003 rockville md ginette y. michaud, m.d. oivd
TRANSCRIPT
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CONSENSUS CONSENSUS STANDARDSSTANDARDS
OIVD WORKSHOPOIVD WORKSHOPApril 22-23, 2003April 22-23, 2003
Rockville MDRockville MD
Ginette Y. Michaud, M.D.Ginette Y. Michaud, M.D.OIVDOIVD
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INTRODUCTIONINTRODUCTION
CDRH recognizes many consensus CDRH recognizes many consensus standards relevant to IVDsstandards relevant to IVDs
IVD SPECIFIC STANDARDSIVD SPECIFIC STANDARDS
GENERIC DEVICE STANDARDSGENERIC DEVICE STANDARDS
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INTRODUCTIONINTRODUCTION
IVD SPECIFIC STANDARDS – NCCLSIVD SPECIFIC STANDARDS – NCCLSautomation and informatics automation and informatics clinical chemistry and toxicologyclinical chemistry and toxicologyevaluation protocolsevaluation protocolsgeneral laboratory practicesgeneral laboratory practiceshematologyhematologyimmunology and ligand assayimmunology and ligand assaymicrobiologymicrobiologymolecular methodsmolecular methods
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INTRODUCTIONINTRODUCTION
““GENERIC” DEVICE STANDARDS-GENERIC” DEVICE STANDARDS-
AAMI, ANSI, CEN, IEC, IEEE, ISO, UL AAMI, ANSI, CEN, IEC, IEEE, ISO, UL softwaresoftwaremedical device risk managementmedical device risk managementhuman factorshuman factorselectrical safety electrical safety electromagnetic compatibility electromagnetic compatibility
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INTRODUCTIONINTRODUCTION
CONSENSUS STANDARDSCONSENSUS STANDARDS
I. Role of consensus standards in IVD I. Role of consensus standards in IVD premarket review premarket review
II. FDA’s role in development of STNDsII. FDA’s role in development of STNDs
III. Process for FDA recognition of STNDsIII. Process for FDA recognition of STNDs
*Focus on consensus documents*Focus on consensus documents
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I. Role of consensus standards I. Role of consensus standards in IVD in IVD premarket reviewpremarket review FDA Modernization Act of 1997FDA Modernization Act of 1997
– Creates Section 514(c) of the Food, Creates Section 514(c) of the Food, Drug, and Cosmetic Act Drug, and Cosmetic Act
FDA recognition of national and FDA recognition of national and international standards (Federal international standards (Federal Register)Register)
voluntary conformance by manufacturers voluntary conformance by manufacturers to recognized standardsto recognized standards
submission of declaration of conformitysubmission of declaration of conformity
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I. Role of consensus standards I. Role of consensus standards in IVD in IVD
premarket reviewpremarket review Conformity with recognized standards may Conformity with recognized standards may
affect:affect:safety and effectiveness determinationssafety and effectiveness determinations
IDE, HDE, PMA, PDPIDE, HDE, PMA, PDP substantial equivalence determinationssubstantial equivalence determinations
510(k)/abbreviated510(k)/abbreviated amount of test data submitted/reviewedamount of test data submitted/reviewed
Manufacturer obligated to:Manufacturer obligated to: maintain recordsmaintain records submit data upon requestsubmit data upon request
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I. Role of consensus standards I. Role of consensus standards in IVD in IVD
premarket reviewpremarket review Conformance to STNDs is voluntaryConformance to STNDs is voluntary Alternate approaches allowedAlternate approaches allowed
Refer to:Refer to: "Recognition and Use of Consensus "Recognition and Use of Consensus
Standards; Final Guidance for Industry and Standards; Final Guidance for Industry and FDA"FDA". . http://www.accessdata.fda.gov/scripts/cdrhttp://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfggp/search.cfmh/cfdocs/cfggp/search.cfm..
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I. Role of consensus standards I. Role of consensus standards in IVD in IVD
premarket reviewpremarket review Other guidance:Other guidance:
"The New 510(k) Paradigm. Alternate "The New 510(k) Paradigm. Alternate Approaches to Demonstrating Approaches to Demonstrating Substantial Equivalence in Premarket Substantial Equivalence in Premarket Notifications, Final Guidance." Notifications, Final Guidance."
and and
"Frequently Asked Questions on the "Frequently Asked Questions on the New 510(k) Paradigm"New 510(k) Paradigm". .
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
Significant OIVD participation in Significant OIVD participation in standards development standards development organizations (SDOs)organizations (SDOs)
official membership by individualsofficial membership by individuals informal document reviewsinformal document reviews
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
FDA SDO participation governed by FDA SDO participation governed by 21CFR10.95 Participation in outside 21CFR10.95 Participation in outside standard-setting activitiesstandard-setting activities. .
– FDA encourages participation if in the FDA encourages participation if in the public interestpublic interest
– CDRH supports participation through the CDRH supports participation through the CDRH Standards ProgramCDRH Standards Program
– Individual participation by invitationIndividual participation by invitation
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
Organization must meet minimum Organization must meet minimum standards as an SDO:standards as an SDO:– activity based on sound scientific and activity based on sound scientific and
technological information; technological information; – revisions on the basis of new information; revisions on the basis of new information; – goal to protect the public against unsafe, goal to protect the public against unsafe,
ineffective, or deceptive products or practices;ineffective, or deceptive products or practices;– activity not for economic benefit of any group;activity not for economic benefit of any group;– activity not involving specific approval of activity not involving specific approval of
individual products;individual products;– existence of commenting procedure. existence of commenting procedure.
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
FDA official participation restricted to FDA official participation restricted to organizations that meet organizations that meet requirements requirements
Standards are considered for FDA Standards are considered for FDA recognition only if developed in recognition only if developed in conformance with requirementsconformance with requirements
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
OIVD participation in standards OIVD participation in standards development: development:
NCCLS NCCLS ISOISOGHTFGHTF
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
NCCLS:NCCLS: international, voluntary, consensus international, voluntary, consensus
SDO SDO Goal: to “enhance the value of Goal: to “enhance the value of
medical testing...through the medical testing...through the development and dissemination of development and dissemination of standards, guidelines, and best standards, guidelines, and best practices” practices”
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
NCCLS Participation:NCCLS Participation:
proposal of new standards projectsproposal of new standards projects committee writing assignmentscommittee writing assignments commenting on documentscommenting on documents voting on proposed standardsvoting on proposed standards
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
International Organization for International Organization for Standardization/ISO:Standardization/ISO:
Voluntary, consensus SDO; non-Voluntary, consensus SDO; non-governmental federation of national SDOs, governmental federation of national SDOs, covering all technical fields except covering all technical fields except electricalelectrical
Mission: to promote international Mission: to promote international standardization to reduce technical standardization to reduce technical barriers to trade barriers to trade
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
ISO:ISO:
~200 technical committees each for ~200 technical committees each for different technical areasdifferent technical areas
OIVD participates in ISO TC 212 OIVD participates in ISO TC 212 Clinical laboratory testing and in vitro Clinical laboratory testing and in vitro diagnostic test systemsdiagnostic test systems
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
ISO TC 212: ISO TC 212: Goal: standardization in laboratory Goal: standardization in laboratory
medicine and IVD test systemsmedicine and IVD test systems 3 working groups:3 working groups:
– WG 1WG 1 Quality management in Quality management in the the clinical laboratory clinical laboratory
– WG 2 WG 2 Reference systemsReference systems– WG 3 WG 3 In vitro diagnostic productsIn vitro diagnostic products
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
ISO TC 212: ISO TC 212: 4 completed standards: 4 completed standards:
– medical laboratory quality and medical laboratory quality and competencecompetence
– reference measurement proceduresreference measurement procedures– reference materialsreference materials– labeling of staining reagentslabeling of staining reagents
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
ISO TC 212: ISO TC 212: Standards under development:Standards under development:
laboratory safety laboratory safety requirements for reference requirements for reference
measurement laboratories measurement laboratories metrological traceabilitymetrological traceability
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
ISO TC 212: ISO TC 212: Documents under development Documents under development
(continued):(continued):requirements for blood glucose self-requirements for blood glucose self-
testing systems testing systems specifications for self-testing specifications for self-testing
Prothrombin Time instruments Prothrombin Time instruments quality management of point of care quality management of point of care
testingtesting
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
Global Harmonization Task Force Global Harmonization Task Force (GHTF):(GHTF):
voluntary multi-national organizationvoluntary multi-national organization representatives: medical device representatives: medical device
regulatory authorities and industry regulatory authorities and industry associationsassociations
Goal: harmonization and convergence Goal: harmonization and convergence of medical device regulatory practices of medical device regulatory practices
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
GHTF: GHTF:
publishes harmonized documents on publishes harmonized documents on regulatory practices & definitions regulatory practices & definitions
for use by emerging economies and for use by emerging economies and developed nationsdeveloped nations
4 Study Groups focused on all phases 4 Study Groups focused on all phases of product life cycleof product life cycle
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
GHTF:GHTF: Harmonization projects:Harmonization projects:
premarket regulatory practices,premarket regulatory practices,standardized premarket submission standardized premarket submission
format,format,labeling requirements labeling requirements data collectiondata collectionpost-market surveillance reporting post-market surveillance reporting
systems systems quality system requirementsquality system requirementsmedical device auditing processesmedical device auditing processes
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II. FDA’s role in the development II. FDA’s role in the development of consensus standardsof consensus standards
CDRH active in all Study Groups (SG); CDRH active in all Study Groups (SG); OIVD active in SG 1 OIVD active in SG 1
SG1: operational aspects of medical SG1: operational aspects of medical device regulation including IVD productsdevice regulation including IVD products
Current IVD harmonization projects:Current IVD harmonization projects: classification classification labelinglabeling IVD premarket conformity with IVD premarket conformity with
principles for safety and performance principles for safety and performance
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III. Process for FDA Recognition III. Process for FDA Recognition of Consensus Standardsof Consensus Standards
62 IVD Standards recognized by 62 IVD Standards recognized by CDRH (NCCLS)CDRH (NCCLS)
numerous non-IVD standards numerous non-IVD standards recognized recognized
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III. Process for FDA Recognition III. Process for FDA Recognition of Consensus Standardsof Consensus Standards
Mechanisms for proposing CDRH Mechanisms for proposing CDRH recognition of consensus standards:recognition of consensus standards:
1.1. Proposals by CDRH Specialty Task Proposals by CDRH Specialty Task Groups (STG) Groups (STG)
2.2. Proposals submitted by outside Proposals submitted by outside persons and considered by STGpersons and considered by STG
Publication in Federal RegisterPublication in Federal Register
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III. Process for FDA Recognition III. Process for FDA Recognition of Consensus Standardsof Consensus Standards
Specialty Task Groups:Specialty Task Groups:
Review previously recognized Review previously recognized Standards for relevanceStandards for relevance
Prepare list of priorities for new Prepare list of priorities for new projects projects
Propose the revision of existing Propose the revision of existing consensus documentsconsensus documents
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CONCLUSIONCONCLUSION
OIVD acknowledges the importance of OIVD acknowledges the importance of consensus standards:consensus standards:
impact on safety & effectivenessimpact on safety & effectivenessgreater premarket requirement greater premarket requirement
transparencytransparencyreview of submissions facilitatedreview of submissions facilitated
Active OIVD participation in development Active OIVD participation in development & recognition of STNDs& recognition of STNDs
http://www.fda.gov/cdrh/stdsprog.htmlhttp://www.fda.gov/cdrh/stdsprog.html