Training & Events

English French
Zoom

GMP Compliance: Introduction

Description: If you hold an establishment licence, or run an operation governed by Part C, Division 2 of the Food

English Training Session
Zoom

Practical Computerized and Automated System Validation

Two Days Training Session By discussing Patient Risk-based Approach, this Training session focuses on developing and implementing regulated digital and

English French
Zoom

Production Value and Overall Equipment Effectiveness

Overall Equipment Effectiveness (OEE) is a well-established KPI metrics to measure the equipment effectiveness. OEE has been widely used for

English French
Zoom

Data Quality and Integrity Management in GMP Environment

Description: Data management refers to all  activities performed during data lifecycle including but not limited to data policy, documentation, quality,

English French
Zoom

Introduction to EU GMP Annex 11

The EU GMP Annex 11 applies to all forms of computerized systems used as part of a GMP regulated activities.

English French
Zoom

Digital & Computerized System Validation

The V-model has become a standard worldwide methodology for the validation of digital and computerized systems. Regulatory requirements, as well

English French
Zoom

Lean Cleaning Validation

Description:  Streamlining the cleaning validation means reducing waste and variation from the cleaning process. Products, raw materials, ingredients (e.g. APIs),

English French
Zoom

GACP and GMP for Cannabis products

Description: Good agricultural practices (GACP) and good manufacturing practices (GMP) for Cannabis and Cannabis-derived products training session is intended for

French Training Session
Zoom

Gestion de la Qualité du Cannabis

La gestion de qualité au sein des entreprises est une activité cruciale qui a un impact sur l’efficacité,  la qualité,

English French
Zoom

GMP Compliance: Introduction

Description: If you hold an establishment licence, or run an operation governed by Part C, Division 2 of the Food

English French
Zoom

Production Value and Overall Equipment Effectiveness

Overall Equipment Effectiveness (OEE) is a well-established KPI metrics to measure the equipment effectiveness. OEE has been widely used for

English French
Zoom

Data Quality and Integrity Management in GMP Environment

Description: Data management refers to all  activities performed during data lifecycle including but not limited to data policy, documentation, quality,

English French
Zoom

Introduction to EU GMP Annex 11

The EU GMP Annex 11 applies to all forms of computerized systems used as part of a GMP regulated activities.

English French
Zoom

Digital & Computerized System Validation

The V-model has become a standard worldwide methodology for the validation of digital and computerized systems. Regulatory requirements, as well

English French
Zoom

Lean Cleaning Validation

Description:  Streamlining the cleaning validation means reducing waste and variation from the cleaning process. Products, raw materials, ingredients (e.g. APIs),

English French
Zoom

GACP and GMP for Cannabis products

Description: Good agricultural practices (GACP) and good manufacturing practices (GMP) for Cannabis and Cannabis-derived products training session is intended for

French Training Session
Zoom

Gestion de la Qualité du Cannabis

La gestion de qualité au sein des entreprises est une activité cruciale qui a un impact sur l’efficacité,  la qualité,

English French
Zoom

GMP Compliance: Introduction

Description: If you hold an establishment licence, or run an operation governed by Part C, Division 2 of the Food

English Training Session
Zoom

Practical Computerized and Automated System Validation

Two Days Training Session By discussing Patient Risk-based Approach, this Training session focuses on developing and implementing regulated digital and

English French
Zoom

Production Value and Overall Equipment Effectiveness

Overall Equipment Effectiveness (OEE) is a well-established KPI metrics to measure the equipment effectiveness. OEE has been widely used for

English French
Zoom

Data Quality and Integrity Management in GMP Environment

Description: Data management refers to all  activities performed during data lifecycle including but not limited to data policy, documentation, quality,

English French
Zoom

Introduction to EU GMP Annex 11

The EU GMP Annex 11 applies to all forms of computerized systems used as part of a GMP regulated activities.

English French
Zoom

Digital & Computerized System Validation

The V-model has become a standard worldwide methodology for the validation of digital and computerized systems. Regulatory requirements, as well

English French
Zoom

Lean Cleaning Validation

Description:  Streamlining the cleaning validation means reducing waste and variation from the cleaning process. Products, raw materials, ingredients (e.g. APIs),

English French
Zoom

GACP and GMP for Cannabis products

Description: Good agricultural practices (GACP) and good manufacturing practices (GMP) for Cannabis and Cannabis-derived products training session is intended for

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