Training & Events

Training & Events
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),

Training & Events
English French
Zoom

QC Lab Equipment Qualification and Data Integrity

Objectives Analytical equipment and instruments provide important scientific data about manufactured products that serves to ensure that they meet specifications.

Training & Events
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

Training & Events
English French
Zoom

Practical HACCP for Drug and Food Safety

This 4-hour interactive online workshop will enable participants to develop practical knowledge of the principles of HACCP for Drug and

Training & Events
English French
Zoom

Successful Implementation of Data Integrity

Successful Implementation of Data Integrity into Pharmaceutical Quality System – In recent years, US FDA, MHRA, EU GMP, WHO, and Health

Training & Events
English French
Zoom

Best Practices of Quality Risk Management

Quality Risk Management (QRM) principles require the evaluation of risk to patient safety and product quality based on scientific knowledge,

Training & Events
English Training Session
Zoom

Lean Six Sigma Yellow Belt Certification Exam Prep Training

 3 Days Classroom Certification – Objectives: Our Yellow Belt Lean Six Sigma Training Content is an assembly of a comprehensive

Training & Events
English French
Zoom

Risk-based Continued Process Verification

Objectives: The third phase of the process validation life cycle, continued process verification, is the ongoing assurance that the routine

Training & Events
English French
Zoom

Travailler dans un environnement BPF

Objectifs: Revoir les réglementations récentes BPF applicables aux produits cosmétiques, de santé naturels, pharmaceutiques, et alimentaires. Ce cours offre une

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

Training & Events
English French
Zoom

Introduction to USFDA 21 CFR Part 11

The 21 cfr part 11 applies to records in electronic form that are created, modified, maintained, archived, retrieved, or transmitted,

Training & Events
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),

Training & Events
English French
Zoom

QC Lab Equipment Qualification and Data Integrity

Objectives Analytical equipment and instruments provide important scientific data about manufactured products that serves to ensure that they meet specifications.

Training & Events
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

Training & Events
English French
Zoom

Practical HACCP for Drug and Food Safety

This 4-hour interactive online workshop will enable participants to develop practical knowledge of the principles of HACCP for Drug and

Training & Events
English French
Zoom

Successful Implementation of Data Integrity

Successful Implementation of Data Integrity into Pharmaceutical Quality System – In recent years, US FDA, MHRA, EU GMP, WHO, and Health

Training & Events
English French
Zoom

Best Practices of Quality Risk Management

Quality Risk Management (QRM) principles require the evaluation of risk to patient safety and product quality based on scientific knowledge,

Training & Events
French Training Session
Zoom

Lean Management et Lean Six Sigma Ceinture Blanche

Objectifs: Comprendre les bénéfices de cette méthode reconnue, maîtriser le rôle et les responsabilités de chacun des acteurs de l’amélioration

Training & Events
English French
Zoom

Risk-based Continued Process Verification

Objectives: The third phase of the process validation life cycle, continued process verification, is the ongoing assurance that the routine

Training & Events
English French
Zoom

Travailler dans un environnement BPF

Objectifs: Revoir les réglementations récentes BPF applicables aux produits cosmétiques, de santé naturels, pharmaceutiques, et alimentaires. Ce cours offre une

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

Training & Events
English French
Zoom

Introduction to USFDA 21 CFR Part 11

The 21 cfr part 11 applies to records in electronic form that are created, modified, maintained, archived, retrieved, or transmitted,

Training & Events
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),

Training & Events
English French
Zoom

QC Lab Equipment Qualification and Data Integrity

Objectives Analytical equipment and instruments provide important scientific data about manufactured products that serves to ensure that they meet specifications.

Training & Events
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

Training & Events
English French
Zoom

Practical HACCP for Drug and Food Safety

This 4-hour interactive online workshop will enable participants to develop practical knowledge of the principles of HACCP for Drug and

Training & Events
English French
Zoom

Successful Implementation of Data Integrity

Successful Implementation of Data Integrity into Pharmaceutical Quality System – In recent years, US FDA, MHRA, EU GMP, WHO, and Health

Training & Events
English French
Zoom

Best Practices of Quality Risk Management

Quality Risk Management (QRM) principles require the evaluation of risk to patient safety and product quality based on scientific knowledge,

Training & Events
French Training Session
Zoom

Lean Management et Lean Six Sigma Ceinture Blanche

Objectifs: Comprendre les bénéfices de cette méthode reconnue, maîtriser le rôle et les responsabilités de chacun des acteurs de l’amélioration

Training & Events
English Training Session
Zoom

Lean Six Sigma Yellow Belt Certification Exam Prep Training

 3 Days Classroom Certification – Objectives: Our Yellow Belt Lean Six Sigma Training Content is an assembly of a comprehensive

Training & Events
English French
Zoom

Risk-based Continued Process Verification

Objectives: The third phase of the process validation life cycle, continued process verification, is the ongoing assurance that the routine

Training & Events
English French
Zoom

Travailler dans un environnement BPF

Objectifs: Revoir les réglementations récentes BPF applicables aux produits cosmétiques, de santé naturels, pharmaceutiques, et alimentaires. Ce cours offre une

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

Training & Events
English French
Zoom

Introduction to USFDA 21 CFR Part 11

The 21 cfr part 11 applies to records in electronic form that are created, modified, maintained, archived, retrieved, or transmitted,