Upcoming Events

07 Sep 2022

Lean Six Sigma Yellow Belt Certification Exam Prep Training

Zoom

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

19 Sep 2022

Risk-based Continued Process Verification

Zoom

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

27 Sep 2022

Fundamentals of Health Canada Annex 11 to GMP Guide

Zoom

Objectives: Health Canada Annex 11 to GMP (GUI-0050) applies to all forms of computerized systems used as part of Good Manufacturing Practices (GMP) regulated activities.

05 Oct 2022

Travailler dans un environnement BPF

Zoom

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

20 Oct 2022

GMP Compliance: Introduction

Zoom

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

01 Nov 2022

Practical Computerized and Automated System Validation

Zoom

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

15 Nov 2022

Production Value and Overall Equipment Effectiveness

Zoom

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

01 Dec 2022

Data Quality and Integrity Management in GMP Environment

Zoom

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

07 Dec 2022

Introduction to EU GMP Annex 11

Zoom

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

17 Jan 2023

Digital & Computerized System Validation

Zoom

The V-model has become a standard worldwide methodology for the validation of digital and computerized systems. Regulatory requirements, as well as industry guidelines, like GAMP®5,

31 Jan 2023

Lean Cleaning Validation

Zoom

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

22 Feb 2023

GACP and GMP for Cannabis products

Zoom

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

19 Sep 2022

Risk-based Continued Process Verification

Zoom

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

27 Sep 2022

Fundamentals of Health Canada Annex 11 to GMP Guide

Zoom

Objectives: Health Canada Annex 11 to GMP (GUI-0050) applies to all forms of computerized systems used as part of Good Manufacturing Practices (GMP) regulated activities.

05 Oct 2022

Travailler dans un environnement BPF

Zoom

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

12 Oct 2022

Gestion de la Qualité du Cannabis

Zoom

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

20 Oct 2022

GMP Compliance: Introduction

Zoom

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

15 Nov 2022

Production Value and Overall Equipment Effectiveness

Zoom

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

01 Dec 2022

Data Quality and Integrity Management in GMP Environment

Zoom

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

07 Dec 2022

Introduction to EU GMP Annex 11

Zoom

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

17 Jan 2023

Digital & Computerized System Validation

Zoom

The V-model has become a standard worldwide methodology for the validation of digital and computerized systems. Regulatory requirements, as well as industry guidelines, like GAMP®5,

31 Jan 2023

Lean Cleaning Validation

Zoom

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

22 Feb 2023

GACP and GMP for Cannabis products

Zoom

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

07 Sep 2022

Lean Six Sigma Yellow Belt Certification Exam Prep Training

Zoom

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

19 Sep 2022

Risk-based Continued Process Verification

Zoom

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

27 Sep 2022

Fundamentals of Health Canada Annex 11 to GMP Guide

Zoom

Objectives: Health Canada Annex 11 to GMP (GUI-0050) applies to all forms of computerized systems used as part of Good Manufacturing Practices (GMP) regulated activities.

05 Oct 2022

Travailler dans un environnement BPF

Zoom

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

12 Oct 2022

Gestion de la Qualité du Cannabis

Zoom

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

20 Oct 2022

GMP Compliance: Introduction

Zoom

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

01 Nov 2022

Practical Computerized and Automated System Validation

Zoom

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

15 Nov 2022

Production Value and Overall Equipment Effectiveness

Zoom

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

01 Dec 2022

Data Quality and Integrity Management in GMP Environment

Zoom

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

07 Dec 2022

Introduction to EU GMP Annex 11

Zoom

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

17 Jan 2023

Digital & Computerized System Validation

Zoom

The V-model has become a standard worldwide methodology for the validation of digital and computerized systems. Regulatory requirements, as well as industry guidelines, like GAMP®5,

31 Jan 2023

Lean Cleaning Validation

Zoom

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

22 Feb 2023

GACP and GMP for Cannabis products

Zoom

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

WHO WE ARE
SERVICES & SOLUTIONS
TRAININGS & WEBINARS

NEWSLETTER

Processing…
Success! You're on the list.