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Excipact Presentation

The document discusses Excipact certification, a third-party audit scheme for excipient suppliers. It was created to help pharmaceutical companies qualify excipient suppliers in a more efficient manner, as required by regulations. Excipact certification involves auditing excipient suppliers' quality management systems according to GMP and GDP standards. It is intended to provide a standardized way for suppliers to demonstrate commitment to quality and help reduce the burden of multiple audits on suppliers and auditors. The certification process and roles of various organizations involved are described.
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0% found this document useful (1 vote)
100 views

Excipact Presentation

The document discusses Excipact certification, a third-party audit scheme for excipient suppliers. It was created to help pharmaceutical companies qualify excipient suppliers in a more efficient manner, as required by regulations. Excipact certification involves auditing excipient suppliers' quality management systems according to GMP and GDP standards. It is intended to provide a standardized way for suppliers to demonstrate commitment to quality and help reduce the burden of multiple audits on suppliers and auditors. The certification process and roles of various organizations involved are described.
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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BENEFITS OF EXCIPACT CERTIFICATION TO SUPPLIERS, USERS AND PATIENTS

The role in Supplier Qualification

March 2011

Excipact Certification
Mitigating Risk
The current nature and challenges facing excipient supplier audits Excipient supplier qualification and Excipact The status of Excipact and its key components

Excipact - Minimise the Risks, Maximise the Benefits

Excipact Certification
Marketing Authorisation Holders have to qualify their Suppliers
EU Chapter 5 Production Revision:
5.26 The selection, including qualification and approval of suppliers.is an important operation which should involve staff who have a particular and thorough knowledge of the suppliers and the associated risks involved in that starting materials supply chain Suppliers of . certain excipients considered to be high risk materials used as starting materials, should be periodically audited to confirm that they comply with current GMP requirements and that supply chain traceability of the starting material is being maintained. The findings from each audit should be documented, and audit reports should be available for review by Inspectors.

Excipact - Minimise the Risks, Maximise the Benefits

Excipact Certification
Excipient Risk Assessment
Expectation that the MAH performs a risk assessment to classify excipients based on risks to patient safety Two (or more) classifications of excipients Considerations could include:
Past history of supply (experience of supplier) Lower Risk Purpose and function of the Excipient Excipients Route of administration Quantity of Excipient used in the formulation Source of Excipient and supply chain Higher Potential risks to patient Risk Excipients etc
Excipact - Minimise the Risks, Maximise the Benefits

Excipact Certification
Higher Risk Excipient Qualification
Periodic Physical Audit and Audit report available for Inspectors Supply chain included (GDP) Plus (e.g.)
IPEC Excipient Information Package - covering specifics of the Excipient such as manufacturing process flow chart, manufacturing process capability, TSE, Solvent, Genotoxic etc.
Lower Risk Excipients

Higher Risk Excipients

Excipact - Minimise the Risks, Maximise the Benefits

Excipact Certification
Lower Risk Excipient Qualification ?
No periodic audits how often would be enough - once? How would the supply chain be covered? Plus (e.g.)
IPEC Excipient Information Package covering specifics of the Excipient such as manufacturing process flow chart, manufacturing process capability, TSE, Solvent, Genotoxic etc.
Lower Risk Excipients

Higher Risk Excipients

Excipact - Minimise the Risks, Maximise the Benefits

Excipact Certification
But all Excipients have the potential to be a threat
So should we not have some kind of physical audit for all excipients? But all physical audits, and especially periodical ones have a major issue regardless of Excipient classification

Excipact - Minimise the Risks, Maximise the Benefits

Excipact Certification
Issues with Physical Audits
Not enough auditors or days in the year to audit all of the suppliers Dilutes resources from assessing higher risks Suppliers could face 100s of audits requests a year so will refuse to host many The authorities on both sides of the Atlantic have indicated that the use of 3rd party audits is acceptable So a 3rd party audit scheme to aid excipient qualification is beneficial to all Excipact was born
Excipact - Minimise the Risks, Maximise the Benefits

Excipact Certification
Excipact Goals
Acceptance by all stakeholders International: certification accepted globally Certification accessible for as many accredited 3rd party organizations as possible given competent auditors Evolutionary: builds on existing guides and standards Simple: easy to understand and apply for all stakeholders Inclusive: applicable to as many excipients as possible Permits the Supplier to proactively demonstrate commitment to GMP and GDP in the manufacture and supply of their excipient
Excipact - Minimise the Risks, Maximise the Benefits

Excipact Certification
Excipact Structure
Focuses on the excipient supplier quality management system rather than individual excipients Separate sections define requirements for
GMP GDP

And for 3rd Party Audit Organisations


Auditor Competency Requirements Scheme rules

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Excipact Certification
Excipact: Good Manufacturing Practice (GMP)
Annex to ISO 9001 developed from the IPEC-PQG GMP Guide 2006 Builds on the basic Quality Management System required in ISO 9001 and amplifies the requirements to include the GMP principles in the IPEC-PQG GMP Guide Assessment of ISO 9001 and Excipact GMP can be simultaneous

Excipact - Minimise the Risks, Maximise the Benefits

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Excipact Certification
Excipact: Good Distribution Practice (GDP)

Annex to ISO 9001 developed from the IPEC GDP Guide 2006 Annex contains specific requirements for Good Distribution Practices Allowance for different distributor/trader operations In-line with SQAS ESAD Section F&G (www.sqas.org) Where there is overlap, GMP- and GDP Annexes contain same requirements
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Excipact Certification

Quality of auditors is critical


Excipact includes a section devoted to auditor competency using ISO 19011 framework with additional requirements for GMP and GDP Alternative starting routes to qualification possible i.e. experienced in ISO 9001, GMP or GDP Considered best practices e.g. SQA and Qualified Person assessment processes Training Guide included with specific requirements for Excipients
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Excipact Certification
Excipact: Status & Timetable
First Draft completed, issued to membership for comment and review Second draft ready for public and stakeholder review in March 2011 Could you examine and comment on Draft 2? Updated Document by Q3 Creating Excipact as a legal entity, a not for profit organisation

Excipact - Minimise the Risks, Maximise the Benefits

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Excipact Certification
Excipact: Status and Timetable
Signing up 3rd party audit organisations allows Excipact to apply oversight 3rd party audit organisations already providing GMP audits have been surveyed and reacted favourably they already have the auditors (e.g. medical devices, packaging etc) Pilot audits in Q3 Launch in Q4 or early Q1 2012
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Excipact Certification
Excipact - how will it work?
Excipact invites bids from 3rd party audit organisations Legal agreement signed for them to adopt the requirements, including Auditor competency Excipact to train the trainers who will train the auditors

Excipact Website
List of 3rd party audit organisations providing certification Directory of certified excipients suppliers List of certifications suspended and withdrawn

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Excipact Certification
Excipact - how will it work?
Supplier selects 3rd party audit organisation (ideally the one that already provides ISO 9001 certification) Supplier identifies if GMP and or GDP parts are needed Standard ISO certification audit process pre audit, full audit, CAPA, Certification At least Annual surveillance audits and triennial recertification - a frequency likely to be higher than any MAH could manage, even for high risk excipients Costs (financially and time) are comparable to ISO 9001 certification
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Excipact Certification
Excipact - how will it work?
Audit Report lists observations and rates findings as critical, major or minor 3rd Party Technical Experts review audit report and findings, recommend certification if
No critical, no major without CAPA, no minors that indicate failure of quality system element

Audit Report available to pharmaceutical customer from excipient supplier may be redacted to show that confidential information has been hidden but substance of report will not be altered
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Excipact Certification
Excipact - how will it work? Overview of relationships
3RD Party Audit Organisation

Excipient Supplier Excipient Supplier

Excipient user Excipient user

EXCIPACT
3RD Party Audit Organisation

Legal Agreement with 3rd party audit Organisations Publish list and Certificates on website

Agreement with supplier Provides audit report and Certificate Verification audit service

Can verify audit report with 3rd party audit organisation Can verify certificate with Excipact
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Excipact - Minimise the Risks, Maximise the Benefits

Excipact Certification
Excipact - how will it work? Overview of relationships

AUTHENTICATES AUDIT REPORT EXCIPACT


3RD Party Audit Organisation

Excipient Supplier

Excipient user

Legal Agreement with 3rd party audit Organisations Publish list and Certificates on website

Agreement with supplier Provides audit report and Certificate Verification audit service

Can verify audit report with 3rd party audit organisation Can verify certificate with Excipact
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Excipact - Minimise the Risks, Maximise the Benefits

Excipact Certification
Excipact - how will it work? Overview of relationships
AUTHENTICATES CERTIFICATE AND 3RD PARTY AUDIT ORGANISATION EXCIPACT
3RD Party Audit Organisation

Excipient Supplier

Excipient user

Legal Agreement with 3rd party audit Organisations Publish list and Certificates on website

Agreement with supplier Provides audit report and Certificate Verification audit service

Can verify audit report with 3rd party audit organisation Can verify certificate with Excipact
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Excipact - Minimise the Risks, Maximise the Benefits

Excipact Certification
Excipient Supplier Qualification
Excipact provides assurance about the quality management system of the supplier covering GMP and GDP So periodic physical audits of all excipients would be possible Audits of Higher Risk Excipients could then concentrate on the key risk factors the individual excipient
ct xcipa E

Lower Risk Excipients

Higher Risk Excipients

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Excipact Certification
Key Benefits of Excipact
Reduce cost (less audits) of reliable qualification (for supplier and manufacturer) Excipact Standard is specific for Excipients, which is unique and globally accepted by all stakeholders Can be applied to all excipient suppliers Highly visible certification to allow authentication of audit organisations as well as certified excipient suppliers Independent and authority acceptable scheme

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Excipact Certification
Key Benefits of Excipact
Scheme is simple to apply globally (ISO based) and to adjust to risk management Overall supply chain strategy including GMP and GDP It is a dynamic product which continues to be developed according to advancing regulatory requirements Improves quality of drugs and hence patient safety

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Excipact Certification Excipact: Minimize Risks Maximize Benefits


None of this would be possible without the commitment and contributions from the volunteers working in the task forces and those on the steering committee. Many thanks to them. Thank you for your attention!

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