GMP

Good Manufacturing Practices GMP

 

 

Who Should Attend This Course:

 

All personnel in the pharmaceutical, biotechnology and medical device industries whose role is related to product discovery, development and/or manufacturing. It will benefit people who are new to industry. As well as those seeking refresher training in the regulationsthis course is also useful for quality assurance and quality control staff, regulatory affairs professionals, auditors, training andproduction staff, and management interested in effective GMP compliance tools and techniques.

 

Objectives of the training course:

 

To acquire and apply the basic concepts of GMP.

To recognize the importance and necessity of GMP compliance.

To train you in the WHO recommendations and requirements on GMP for manufacturing processes, laboratory activities.

To introduce general elements on quality management.

To bring in your own experience.

To develop the personal action plan to ensure compliance at your company.

 

Content:

 

01- Introduction to the training program.

02- Quality Management in the drug industries.

03- Personnel.

04- Sanitation and hygiene.

05- Premises and equipment.

06- Documentation.

07- Materials.

08- Good practise in production.

09- Good practise in quality control.

10- Complaints and recalls.

11- Self-inspection and quality audits.

12- Validation and Qualification.

 

Study Type:

 

Classroom and Online

 

You can study from anywhere in the world via the Online System. The online lectures are alive transmission of lectures at the same time as the center with enabling the participant to communicate with the lecturer by chat or voice during the lecture and also receiving video records of lectures on the next day of the lecture.

 

Duration:

 

10 lectures , 1 lecture per week , 4 hours per lecture

 

Fees:

 

2000 LE for class

( Can be paid on 2 installments )

 

2500 LE for On Line

( Can be paid on 2 installments )