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5/15/23, 7:00 PM QMS Lead Auditor for the Pharmaceutical Industry | CQI | IRCA

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QMS Lead Auditor for the Pharmaceutical Industry

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Course code
PR330

Duration
40 hours

Category
Auditing

Type
CQI and IRCA Certified Training

Level
Professional

Scheme(s)
Pharmaceutical
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5/15/23, 7:00 PM QMS Lead Auditor for the Pharmaceutical Industry | CQI | IRCA

This course provides comprehensive certification for Auditors in the


Pharmaceutical industry.

Certified by CQI and IRCA and the Pharmaceutical Quality Group (PQG), this Lead Auditor
course has been specifically developed for the pharmaceutical industry.

The course incorporates the principles of performing first, second and third-party audit as an
Auditor/Lead Auditor to the supply chain of pharmaceutical manufacture. In the absence of
having mandatory GMP this course is intended for individuals to acquire the knowledge and
skills to lead audits of suppliers to both GMP and non-GMP utilising PS9000, EXCiPACT, IPEC,
ISO 15378, and ISO 9001 in accordance with ISO 19011, ISO 17021-1, as applicable.

This course includes two examinations:

CQI and IRCA 2-hour written exam

PS9000 1-hour Certification exam

Who is it for?
This course is for those intending to acquire the understand and competence of how to
apply the appropriate standards either as a third or second-party auditor for auditing
pharmaceutical suppliers:

PS9000 for packaging components

EXCiPACT and IPEC/PQG GMP for Excipients

EU GMP Part II for APIs, ISO 15378 for primary packaging components

Successful completion of this course provides learners with a qualification in auditing that is
recognised by the PQG.  Successful completion of this course also meets the training
requirement for certification as an auditor on IRCA's PQMS Auditor Certification scheme.

Recommended Prior Knowledge


FD116: QMS ISO 9001:2015 Foundation

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5/15/23, 7:00 PM QMS Lead Auditor for the Pharmaceutical Industry | CQI | IRCA

Knowledge of  ISO 9001, ISO 15378, PS9000, IPEC and EXCiPACT standards is desirable
prior to the course. It is also desirable you have some knowledge in the following areas:
Quality Management Systems and the core elements of a management system and the
interrelationship between top management responsibility, policy, objectives, planning,
implementation, measurement, review and continuous improvement. The quality
management principles (see ISO 9000) are also desirable and the relationship between
quality management and customer satisfaction and ISO 9001.

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Tags

Assurance | Auditing | Auditor/Lead Auditor | Pharmaceutical

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