Courses and seminars
Gstudy > Courses and seminars
Professional courses, workshops, and seminars, in a variety of fields, provide knowledge and acquaintance with the relevant regulatory requirements and provides the tools for their practical application. The wide variety allows each employee, new or experienced, to choose a topic to specialize in the workplace by implementing highlighted issues based on our field experience. The courses include case studies and group workshops.
Qualification of Validation Engineers in Pharmaceutical Industry for Systems and Equipment Course
Mar 27, 2025
By Elias Morany, M.Sc. & Jose (Yossi) Chvaicer, M.Sc.
מחזור 7
Location: Online + Frontal
Duration: 3 Meetings
Starts at: 09:30
Language: Hebrew
The training includes a comprehensive overview of the validation life cycle for systems andequipment in the pharmaceutical industry according to the cGMP requirements. The training provides you with the latest regulatory aspects, validation life cycle review, DQ/...
Cleaning Validation Seminar for Pharmaceuticals Industry With Iris Shamir
May 5, 2025
By Iris Shamir, M.Sc.
מחזור 3
Location: Frontal
Duration: 1 Meeting
Starts at: 09:00
Language: Hebrew
The seminar will review the regulatory requirements and guidelines of cleaning validation lifecycle.In the seminar we will learn about examples of authorities observations, how to avoid common mistakes and practice. The topics of the seminar: Seminar date –...
Qualification of analytical lab staff
By Rivka Goldik, D.Sc.
1
Location: Frontal
Duration: 3 Meetings
Starts at: 09:30
Language: עברית
The course is intended to prepare the analytical staff in a GMP lab. The participants will receive useful information about various topics including the Pharmacopoeias, correct use of equipment, and ranking from volumetric apparatus to HPLC. How will I benefit? and why...
Internal and External Auditors Course for the Pharmaceutical Industry with Iris Shamir
By Iris Shamir, M.Sc.
מחזור 1
Location: Frontal
Duration: 2 Meetings
Starts at: 09:00
Language: Hebrew
Internal and External Auditor Seminar for the Pharmaceutical Industry, based on ISO19011 Principles and the applicable FDA and EU regulations.Focus on Audit of API Manufacturers based on Q7A requirements, and Audit of Excipient Manufacturers. With actual examples,...
