Upcoming Events 2024
Montreal - Quebec City - Toronto - Vancouver - New Jersey
New York - San Francisco - Rio De Janeiro - Buenos Aires - Beijing - Shanghai - Cairo Egypt
Global Scheduled Events
Register online for Courses/ Live Seminars/ Webinars and Workshops
2024
Courses marked virtual can be taken on internet. For more information please click here
Courses marked On-Site are arranged at your plant. For more information please contact us click here
BootCamps-Events
Boot Event
Date and Type
Location and Language
Description
Modern Management Boot Camp
May 6-10, 24
virtual
Live
Global
English
Includes FIVE courses:
The new Manager , Using Time Effectively , Leadership in Action, Problem Solving-decision marking , Project Management , in addition ,includes scenarios, video situation analysis and workshops the best in the industry.
Click here for more information
AI enhanced Computer System Validation (CSV) Boot Camp
for Pharmaceutical and biopharmaceutical
May 20-24, 24
virtual
Live
Global
English
Includes THREE courses:
Chat GPT , Modern CSV, Advanced CSV and Network Validation
plus three workshops
Click here for more information
AI enhanced Modern Validation Technology Boot Camp
for Pharmaceutical and biopharmaceutical
Apr. 15-19, 24
virtual
Live
Global
Bilingual
Includes Four courses:
Chat GPT , New Process validation, Cleaning Validation, Facility & equipment Qualification, modern Risk analysis,
Click here for more information
AI Risk Based Quality Assurance Boot Camp
for Pharmaceutical and biopharmaceutical
Apr.22-26, 24
virtual
Live
Your Computer
Your Site
Includes THREE courses:
Chat GPT, Techniques of Risk Analysis , GMP a Risk Based Approach, Essentials of Modern Process Validation
Click here for more information
Liquid Chromatography Plus QbD Boot Camp
for Pharmaceutical and biopharmaceutical
virtual
Live
Global
English
IncludesFour courses:
Modern LC, Advanced LC,Modern Method Development + Analytical Quality by Design, for brochure
Click here for more information
Modern Management Courses
Event
Date and Type
Location, Language, & Course Code
Description
Problem Solving
May1, 24
virtual
Global
English/French
EMA8
problems ! decisions! learn techniques of problem solving and prevention and work on short and long term solutions
Click here for more information
Dynamic Project Management
May 8, 24
virtual
Global
English/French
DPM
This course will provide you with effective modern techniques to handle difficult projects and meet objectives and deadlines.
Click here for more information
Leadership in Action
May 15, 24
virtual
Global
English/French
EMA3
Leaders are not born nowadays, they are made, learn how to become an effective inspiring leader.
Click here for more information
Using Time Effectively
May 22, 24
virtual
Live
Global
English/French
EMB1
Learn time management skills,do it ,manage it and eventually have it in your system, Effectively
Click here for more information
Developing Effective Teams
May 22 , 24
virtual
Live
Global
English/French
EMA6
Work places are being changed to make things better for workers and to increase productivity , its called improving the quality of work life. this one day course will provide you with with essentials tools for building effective teams.
Click here for more information
The New Supervisor : how to be effective and efficient
Apr.17, 24
virtual
Live
Global
English/French
EMA9
This course is especially designed for new supervisor who wants to be effective from Day one
Click here for more information
Managing Conflict
Apr.24, 24
virtual
Global
English/French
MCE
This course will provide you with effective modern techniques to manage conflict to reach a a status of W/W
Click here for more information
Analytical-HPLC Courses
Event
Date and Type
Location, Language, & Course Code
Description
Modern HPLC
Theory and Practice
for pharmaceutical, biopharmaceutical and environmental
May 2-3, 24
virtual
Global
English
MHPLC2
If you use HPLC as part of your everyday on-the-job function and you want to learn more about the new techniques, instrumentation ,troubleshooting, instrumentation qualification and much,much more then you should consider this course.
Click here for more information
Advanced HPLC
Theory and Practice
for pharmaceutical, biopharmaceutical and environmental
May 6-7, 24
virtual
Global
English
MHPLC3
This course is especially designed for the chromatographer who wants to expand his liquid chromatography knowledge especially regarding advanced LC concepts and techniques. you will also learn how to use LC computer modeling to solve separation problems without even using the laboratory this course should not be missed.
Click here for more information
Modern strategies for LC Method Development
for pharmaceutical, biopharmaceutical and environmental
May 13-14, 24
virtual
Live
Global
English
MHPLC4
New development and new strategies for HPLC method development techniques for most recent LC innovation such as ultrahigh speed,new column technologies, new case studies and new techniques to solve multicomponents chromatograms are all included in this course. The course is designed for chromatographers with at least 2 years of experience or candidates who have attended our modern and advanced HPLC2 and HPLC3 courses.
Click here for more information
Quality by Design approach to LC Method Development
for pharmaceutical industry
May 23-24, 24
virtual
Live
Global
English
QLDHPLC5
QbD principles have been applied to the development of analytical methods similar to process QbD, the result of AQbD is a well understood, fit for purpose, and robust method that consistently delivers the intended performance throughout its lifecycle. The course is designed to provide you with the most recent application of QbD concept for LC method development
Click here for more information
Technical Courses
Event
Date and Type
Location, Language, & Course Code
Description
AI enhenced Risk Based Modern Cleaning Validation: A 360 Approach
for pharmaceutical and biopharmaceutical industries
May 22-23-24, 24
+ Workshop
Montreal
English
MCPV
This course will provide a solid overview of the principles and technology of residue removal and residue measurement on product contact surfaces. It will address the latest issues, industry practices and compliance strategies regarding choice of cleaning techniques, cleaning agents, analytical methods, residue challenges, grouping strategies and validation protocols. Examples of current industry cleaning validation practices and case histories will be presented.
Click here for more information
Quality by Design in Pharmaceutical Manufacturing+ Practical Applications
May 16-17, 24
Global
English
RPQS
The course was designed for the pharmaceutical, professionals with the responsibilities in pharma design, operation , management of the quality system, compliance and CMC application. learn all about the QbD requirement and how it relates to ICHQ8 and Q9 and how to integrate the different components effectively for a complete robust manufacturing system and relate it to Q 10. + practical applications.
Click here for more information
Data Integrity for Pharma and Biopharma
Strategies and Workshop
May 27-28, 24
Virtual
Live
Global
English
DIV4
Data integrity issue is so hot that every pharmaceutical company would be very interested to know more about and how to master compliance. it is therefore important for every pharmaceutical company to know all the guidelines that are applicable for data integrity, and know how to apply and interpret data to reach complete compliance. Facing a data issue during inspection is not easy to handle and serious noncompliance is inevitable. Learning how data flows in different discipline and knowing The Effective implementation of regulatory guidelines, whether it is FDA, EMA or WHO guidelines need to be interpreted the right way to assure the accuracy precision and consistency of data. We will handle all issues related to data integrity in this live conference to provide you with the proper methodology of handling data and to increase your understanding of data integrity issues. Our course will build you confidence with many workshops exercises to provide you with the necessary practical issues and the right way to handle them, whether in the Laboratory, Manufacturing or validation, along with how to evaluate the risk involved.
Click here for more information
Risk Based Modern Aseptic Processing
for pharmaceutical , biopharmaceutical industries
June 6-7, 24
Two day-Course
virtual
Montreal
English
RBMAP
This course is designed to provide you with an update of practices and technologies that are shaping today's pharmaceutical and biopharmaceutical aseptic processing. Modern aseptic processing require attention to many details of which many sterile companies miss and fall into non-compliance. This course covers all the concepts, techniques and regulatory requirements that will facilitate the personnel training and solid understanding of aspetic processing
Click here for more information
AI powered Modern Design of Experiments
for pharmaceutical , biopharmaceutical industries
Apr.20-21, 24
Two day-Course
Montreal
English
DOEW
Learning how to do design of experiments (DOE) using GPT 4 will provide you with a fast real solution and solid decision making instead of changing one separate factor at a time (OFAT) does not lead to the real optimum solution, and gives different implications with different starting points. Learn how to use AI designed to provide fast and easier practice of DOE. This course is packed with examples and practice problem solving exercises related to pharmaceutical : QbD, development , optimization as well as QC and validation.
Click here for more information
Modern cGMP courses
Event
Date and Type
Location, Language, & Course Code
Description
Pharmaceutical GMP for 21st Century. A Risk Based Approach
On-site
Virtual
your plant/your computer
Bilingual
GMP-RBA
This course will provide you with the latest modern approach the FDA has initiated. modules will be presented and how the FDA is applying the system.
Click here for more information
cGMP for Natural Products
Virtual
virtual course
your computer
English
GMP-NP
This course is designed to provide cGMP training ,as per HPFB ,for production and QA personnel working in the manufacturing of Natural products.
Click here for more information
cGMP for sterile manufacturing
Virtual
virtual course
your computer
Bilingual
GMP-S
This course is designed to provide cGMP training ,as per HPFB and FDA ,for sterile manufacturing personnel working in pharmaceutical and biopharmaceutical.
Click here for more information
cGMP for non-sterile manufacturing
Virtual
one-day course
your computer
Bilingual
GMP-NS
This course is designed to provide cGMP training ,as per HPFB and FDA ,for non-sterile manufacturing personnel working in pharmaceutical and allied industries.
Click here for more information
cGMP for Active Pharmaceutical Ingredient Manufacturing
Virtual
one-day course
your computer
Bilingual
GMP-API
This course is designed to provide cGMP training ,as per ICH ,for production , QA , personnel working in Bulk chemical Manufacturing.
Click here for more information
Equipment Qualification / Modern and Advanced Process Validation Courses
Event
Date and Type
Location, Language, & Course Code
Description
HPLC Equipment Qualification
Virtual
virtual course
your computer
English
LC_EQ
This course will clarify the why, what and how to qualify HPLC systems as per the USP new Guidelines
Click here for more information
Equipment and Facility Qualification
Virtual
virtual course
your computer
English
EFQL
This course will clarify the why,what and how to qualify equipment as well as facility, in the pharmaceutical ,biopharmaceutical and Bulk Chemical manufacturing and systems qualification
Click here for more information
How to Qualify a Tablet Press?
Virtual
virtual course
your computer
English
TPQL
This course will go into details of IQ,OQ and PQ of a Tablet Press
Click here for more information
Modern Process Validation
for pharmaceutical and biopharmaceuticals
Virtual
Live
Global
English
MPV
This is the ultimate course for the essentials of process validation for pharmaceuticals and biopharmaceuticals. Enjoy the superior quality of world experts in the filed of validation and get challenging problem solving workshops.
Click here for more information
Advanced Process Validation I
in a Quality by Design Approach
Virtual
Live
Global
English
AMPVI
In the first day two workshops will be take place ,in a quality by Design approach , the role of blend uniformity in process validation and the afternoon workshop will discuss statistical tools for process validation, in the 2nd day topics such as regulatory requirement, integration of process validation, PAI and technology transfer, process capability and process capability index will be discussed.
Click here for more information
Advanced Process Validation II
Virtual
Live
Global
English
AMPVII
This course will discuss in the first day process validation failures for non-sterile manufacturing , process validation of raw materials. the second day process validation as a critical component of pharmaceutical manufacturing, how prospective, retrospective and revalidation approaches differ, fractional factorial designs,how to validate a suspension?
Click here for more information
Advanced Process Validation III
Virtual
Live
Global
English
AMPVIII
In this course validation master plan will be discussed in details along with VP and report, also PAI and technology transfer will be discussed in relation to process validation, more emphasis will be on the process validation of non-sterile manufacturing in the afternoon., day two will discuss equipment qualification, v-blender, autoclave and a case studies and workshops.
Click here for more information
Advanced Process Validation IV
Virtual
Live
Global
English
AMPVIV
This course will discuss :Develop sound understanding of Validation streamlining. How to properly characterize a process and when? Learn how to establish valid sampling, testing and release specifications, Learn the important factors in cleaning validation and how to analyze data? Get in-depth knowledge about PAT and how will it change the validation paradigm? Discover the strategies for how to implement PAT in pharmaceutical manufacturing? and how to use risk management techniques in process validation.
Click here for more information
Advanced Process Validation V
Virtual
Live
Global
English
AMPVV
The advanced subjects discussed in this course include: stratified sampling for blend uniformity,Problems encountered with equipment qualification,Techniques of Risk analysis and process validation , PAT, Radio Frequency Identification (RFID) - Counterfeit pharmaceuticals, Process design and data analysis for cleaning validation
Click here for more information
Advanced Process Validation V
Virtual
Live
Global
English
AMPVV
The advanced subjects discussed in this course include:
-Develop a good understanding of compliance master planning
-Learn how to troubleshoot validation master plans
-Develop a good understanding of the modern ways to maintain the validated state
-Develop in-depth understanding of how to apply FMEA risk technique in oral dosage forms.
-Discover how-to do facility Validation
-Learn how to establish packaging validation, which is critical to business compliance
-Learn the important factors in cleaning validation and how to analyze data?
-Learn about automated equipment and process control system validation.
-Get in-depth knowledge about PMQ master Plan
Click here for more information
Computer and Software System Validation Courses
Event
Date and Type
Location, Language, & Course Code
Description
Validation of computer and software system
Virtual
Live
Global
English
VCSV
This 2-day course for Computer system validation will allow an excellent start-up for computer validation
Click here for more information
Advanced Computer and Software Validation
Virtual
Live
Global
English
ACSV
This course is designed to bring to the IT ,QA pharmaceutical professional the latest development in computer and software validation check here to see the 10 reason why you should not miss this course if you are in computer validation.
Click here for more information
Corporate computer Systems Network Validation
Virtual
Live
Global
English
NV
This is a special session course for Network validation which is the backbone of your infra-structure of the company , it is not only a regulatory requirements but also an essential part of your validation projects, it includes Cloud Computing Validation.
Click here for more information
Validation Strategies for ERP
Virtual
Live
Global
English
VERP
This is a special session course for Validation of ERP systems which is considered the backbone of the management systems of the company , it is not only a regulatory requirements but also an essential part of your validation projects. Our intensive two days course will provide you with an update of practices and technologies that are shaping today’s pharmaceutical and biopharmaceutica and medical devices l computer validation needs.
Click here for more information
Upcoming Webinars
Event
Date
Location, Language, & Course Code
Description
ChatGPT for Pharma and Biopharma
Apr. 24, 24
9am-12pm;
1pm-4pm EST
Internet
English
AIWeb
This is a two-parts webinar each of 3-hours provides a practical approach to Chat GPT use & for pharma/Biopharma.
Click here for more information
Modern Risk Based Analysis for Pharma Analytical Laboratory
May 1, 24
10:00am -12:00pm EST
Internet
English
TTWeb
How to to apply modern Risk analysis in the analytical Lab. with meaniful results that really help
Click here for more information
Medical Devices
Event
Date
& Type
Location, Language, & Course Code
Description
Modern Sterilization techniques for Medical devices
Virtual
Live
Global
English
MdST
Medical devices sterilization techniques are diversified , learn in this course the modern techniques used presently in North America and Europe. Learn what to choose, to validate and your best options for compliance.
Click here for more information
Techniques of Risk Analysis
for Medical Devices
Virtual
Live
Internet
English
MdTRA
Learn about the risk analysis techniques and how to use them for medical devices the what , how and when to apply these techniques and how to use ISO/IEC 14971 for medical device.
Click here for more information
Quality Management: Six Sigma and Lean Six Sigma
Event
Date
& Type
Location, Language, & Course Code
Description
Pharmaceutical Quality Risk Based compliance
for pharmaceutical and biopharmaceutical
Jun. 13-14, 24
Live
Global
English
PRBC-2
This course is especially designed to address how to use risk management in the pharmaceutical industry as per ICH Q9 , in addition you will learn detailed risk techniques , risk assessment, risk analysis and how to apply to process validation , analytical method validation cleaning validation , for sterile and non-sterile manufacturing.
Click here for more information
Quality Improvement Process
for pharmaceutical, biopharmaceutical, and medical devices
Jul. 11-12, 24
Virtual
Live
Global
English
QS201
Everybody talks about QIP , very few companies apply the real five stages of QI. Learn the tools, techniques and how to really install and pioneer a QIP in your company.
Click here for more information
Quality Systems
design and management
for pharmaceutical and biopharmaceutical
Jun. 10-11, 24
Virtual
Live
Global
English
QS201
FDA and HPFB are using a new approach for inspection, they inspect your quality system. Know the difference of Quality vs. Quality by design , how to use risk management and risk assessment, what is the efficient way to handle CAPA and how FDA uses the Six-system inspection model. Learn how to apply quality systems models to product and processes , packaging and nonconformance
Click here for more information
Lean Six Sigma For Pharma the easy way!
Jun. 20-21, 24
Virtual
Live
Global
English
LSSPA
lean six sigma as process improvement methodology lead to impressive results that had been proven consistently over and over in thousands of projects across hundreds of businesses. The difference is how much success? Some organizations struggle to capture the big savings and others gain quite easily. Some organizations are slow to gain momentum; others see the organizational change in a matter of months. Learn from deployment professional the key factors that impact return on investment which can turn a mediocre program into the next big talking.
Click here for more information
-
Check our new course list added to our virtual training center
-
Check our list of courses offered on-site check and why should you consider it ?
-
Here is some of our company list that have attended courses before and are more than happy in fact they are always in touch with us since 1985