Workshop: OLT.26.07.01 ABGESAGT: Good Manufacturing Practice (GMP, GLP und GCP) basics and extended requirements in the pharmaceutical environment 07/08.07.26 - Details

Workshop: OLT.26.07.01 ABGESAGT: Good Manufacturing Practice (GMP, GLP und GCP) basics and extended requirements in the pharmaceutical environment 07/08.07.26 - Details

General information

Course name Workshop: OLT.26.07.01 ABGESAGT: Good Manufacturing Practice (GMP, GLP und GCP) basics and extended requirements in the pharmaceutical environment 07/08.07.26
Subtitle
Course number OLT.26.07.01
Semester SoSe2026
Current number of participants 20
expected number of participants 20
Home institute Graduate School Science, Medicine and Technology (Oltech)
Courses type Workshop in category Teaching
First date Tuesday, 07.07.26, 09:00 - 17:00 o'clock
Type/Form
Lehrsprache englisch
ECTS points 1

Rooms and times

No room

  • Tuesday, 07.07.26, 09:00 - 17:00 o'clock
  • Wednesday, 08.07.26, 09:00 - 17:00 o'clock

Module assignments

Comment/Description

This workshop has been cancelled and will be rescheduled for a later date. Registered participants will retain their places.

Lecturers: Dr. Heinrich Prinz (PDM-Consulting)

In this workshop, you will learn the basic requirements for a quality management system and gain insight into concrete activities, such as risk analysis for a manufacturing process and conducting audits in the quality assurance environment of a pharmaceutical product. You will also learn about the requirements of clinical trials, which are a basic prerequisite for the marketability of pharmaceuticals. You will learn in detail, which activities and tasks quality control must fulfill and cover in a pharmaceutical company. The distinction between quality assurance, manufacturing and the tasks of the legally responsible persons, in particular the Qualified Person, is important here.
 Regulatory requirements for the manufacturing of drugs (Content and structure of the regulations for the manufacturing of drugs in respect to development, production, registration and distribution)
 What does GMP mean – „What do I need to know about GMP in the pharmaceutical environment? What are the differences between GMP – GLP – GCP
 Legal Responsibilities
 GMP and Quality Management
 GMP and the Production of a Medicinal Product
 GMP and the Quality Control of Medicinal Product
 Performance of clinical trials
 ATMP’s, Protein Engineering, Tissue Engineering
 Medical devices, Combination products

Lecturer
Dr. Heinrich Prinz studied chemistry and genetics and worked for many years in the pharmaceutical industry, where he was responsible for quality management in the pharmaceutical, medical devices and diagnostics sectors. His main focus is on the development and implementation of quality management systems according to GMP Part I and II and integrated management systems as well as the execution of audits and trainings. With PDM-Consulting he advises companies in the production of pharmaceuticals, medical devices and in-vitro diagnostics regarding quality management and trains employees as well as doctoral candidates.

Location: Presence

Registration mode

After enrolment, participants will manually be selected.

Potential participants are given additional information before enroling to the course.

The enrolment is binding, participants cannot unsubscribe themselves.