GMP Guides for QA Managers | Audit, CAPA, Quality System

Operational Guide to the Role of the QA Manager in the Pharmaceutical Industry

Operational Guide to the Role of the QA Manager in the Pharmaceutical Industry

Regular price €149,00 EUR

Regular price ~~€0,00 EUR~~ Sale price €149,00 EUR
ALCOA+ & Data Governance – The Definitive Operational Guide for Pharmaceutical Data Integrity

ALCOA+ & Data Governance – The Definitive Operational Guide for Pharmaceutical Data Integrity

Regular price €49,00 EUR

Regular price Sale price €49,00 EUR
SOP: Self-Inspections in the Pharmaceutical Sector

SOP: Self-Inspections in the Pharmaceutical Sector

Regular price €39,00 EUR

Regular price Sale price €39,00 EUR
ICH Quality Guidelines Q – The Complete Guide to Q8, Q9, Q10, Q12

ICH Quality Guidelines Q – The Complete Guide to Q8, Q9, Q10, Q12

Regular price €89,00 EUR

Regular price Sale price €89,00 EUR
Data Integrity in QC Labs – HPLC, GC, Empower, LIMS, ELN

Data Integrity in QC Labs – HPLC, GC, Empower, LIMS, ELN

Regular price €49,00 EUR

Regular price Sale price €49,00 EUR
Audit Trail Review Step-by-Step – The Definitive Operational Guide for QC and Manufacturing

Audit Trail Review Step-by-Step – The Definitive Operational Guide for QC and Manufacturing

Regular price €49,00 EUR

Regular price Sale price €49,00 EUR
PIC/S PI Documents, Aide-Memoires and Operational Guidelines: How to Read, Interpret and Apply Them

PIC/S PI Documents, Aide-Memoires and Operational Guidelines: How to Read, Interpret and Apply Them

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Introduction to PIC/S: Structure, Functioning, Documents and Aide-Memoires

Introduction to PIC/S: Structure, Functioning, Documents and Aide-Memoires

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How to Prepare for a PIC/S Inspection – Operational Audit-Ready Guide

How to Prepare for a PIC/S Inspection – Operational Audit-Ready Guide

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Regular price Sale price €49,00 EUR
GMP Deviations & CAPA: Effective Implementation and Audit Defensibility (EU GMP, FDA, AIFA, ICH Q10)

GMP Deviations & CAPA: Effective Implementation and Audit Defensibility (EU GMP, FDA, AIFA, ICH Q10)

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Internal GMP Audits: how to make them effective, risk-based, and defensible during AIFA/FDA/EMA inspections

Internal GMP Audits: how to make them effective, risk-based, and defensible during AIFA/FDA/EMA inspections

Regular price €129,00 EUR

Regular price Sale price €129,00 EUR

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Operational Guide to the Role of the QA Manager in the Pharmaceutical Industry

Operational Guide to the Role of the QA Manager in the Pharmaceutical Industry

ALCOA+ & Data Governance – The Definitive Operational Guide for Pharmaceutical Data Integrity

ALCOA+ & Data Governance – The Definitive Operational Guide for Pharmaceutical Data Integrity

SOP: Self-Inspections in the Pharmaceutical Sector

SOP: Self-Inspections in the Pharmaceutical Sector

ICH Quality Guidelines Q – The Complete Guide to Q8, Q9, Q10, Q12

ICH Quality Guidelines Q – The Complete Guide to Q8, Q9, Q10, Q12

Data Integrity in QC Labs – HPLC, GC, Empower, LIMS, ELN

Data Integrity in QC Labs – HPLC, GC, Empower, LIMS, ELN

Audit Trail Review Step-by-Step – The Definitive Operational Guide for QC and Manufacturing

Audit Trail Review Step-by-Step – The Definitive Operational Guide for QC and Manufacturing

PIC/S PI Documents, Aide-Memoires and Operational Guidelines: How to Read, Interpret and Apply Them

PIC/S PI Documents, Aide-Memoires and Operational Guidelines: How to Read, Interpret and Apply Them

Introduction to PIC/S: Structure, Functioning, Documents and Aide-Memoires

Introduction to PIC/S: Structure, Functioning, Documents and Aide-Memoires

How to Prepare for a PIC/S Inspection – Operational Audit-Ready Guide

How to Prepare for a PIC/S Inspection – Operational Audit-Ready Guide

GMP Deviations & CAPA: Effective Implementation and Audit Defensibility (EU GMP, FDA, AIFA, ICH Q10)

GMP Deviations & CAPA: Effective Implementation and Audit Defensibility (EU GMP, FDA, AIFA, ICH Q10)

Internal GMP Audits: how to make them effective, risk-based, and defensible during AIFA/FDA/EMA inspections

Internal GMP Audits: how to make them effective, risk-based, and defensible during AIFA/FDA/EMA inspections

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