.Courses marked virtual can be taken on internet for more information please Click here urs

..................Courses marked On-Site are arranged at your plant for more information please contact us Click here .L...................

BootCamps-Events ...h TOP

Modern Management Courses ............... TOP

Analytical- HPLC Courses ..........TOP

Event	Date	Type	Location	Course Code	Language	Description
Modern HPLC Theory and Practice for pharmaceutical,biopharmaceutical and environmental	Oct. 5-6, 23 virtual	virtual	Global	MHPLC2	English	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	Oct, 13-14,23 virtual	virtual	Global	MHPLC3	English	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	Oct. 20-21,23 virtual	Live	Global	MHPLC4	English	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 the pharmaceutical industry	Oct. 23-24, 23 virtual	Live	Global	QLDHPLC5	English	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 fClick here for more information

Technical Courses ............... TOP

Modern cGMP courses ............... TOP

Event	Date	Type	Location	Course Code	Language	Description
Pharmaceutical GMP for 21st Century. A Risk Based Approach	On site/ virtual	on site/online	your plant/your computer	GMP-RBA	Bilingual	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	GMP-NP	English	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	GMP-S	Bilingual	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	GMP-NS	Bilingual	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	GMP-API	Bilingual	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 ............... TOP

Event	Date	Type	Location	Course Code	Language	Description
HPLC Equipment Qualification	virtual	virtual course	your computer	LC_EQ	English	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	EFQL	English	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	TPQL	English	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	MPV	English	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	AMPVI	English	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	AMPVII	English	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	AMPVIII	English	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	AMPVIV	English	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	AMPVV	English	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 VI	virtual	Live	Global	AMPVVI	English	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 ..+............. TOP

Event	Date	Type	Location	Course Code	Language	Description
Validation of computer and software system	virtual	Live	Global	VCSV	English	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	ACSV	English	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	NV	English	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	VERP	English	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 ...TOP.........

Event	Date	Location	Course Code	Language	Description
ChatGPT for Pharma and Biopharma	Oct. 18,23	Internet	AIWeb	9am-12pm ; 1pm-4pm EST English	This is a two-parts webinar each of 3-hours provides a practical approach to ChAT GPT use & for pharma/Biopharma. .click for more information
Modern Risk Based Analysis for Pharma Analytical Laboratory	Oct. 25, 23	internet	TTWeb	10:00am -12:00pm EST English	How to to apply modern Risk analysis in the analytical Lab. with meaniful results that really help Click for more information

Medical Devices .................................TOP

Event	Date	Type	Location	Course Code	Language	Description
Modern Sterilization techniques for Medical devices	virtual	Live	Global	MdST	English	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	Global	MdTRA	English	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................... TOP

 

Event	Date	Type	Location	Course Code	Language	Description
Pharmaceutical Quality Risk Based compliance for pharmaceutical and biopharmaceutical	Oct. 25-26, 23	Live	Global	PRBC-2	English	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	Nov. 1-2, 23 virtual	Live	Global	QS201	English	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	Nov. 6-7, 23 virtual	Live	Global	QS102	English	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!	Nov. 15-16, 23 virtual	Live	Global	LSSPA	English	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