Good Laboratory Practice

A workshop offered by the Bonn Graduate Center.

Good Laboratory Practice (GLP) is a quality assurance system concerned with the organizational process and the conditions under which non-clinical health and environmental safety studies are planned, performed, monitored, recorded, archived and reported. 

The purpose of this course is to promote the development of quality test data and provide a tool to ensure a sound approach to the management of laboratory studies, including planning, conduct, data evaluation, reporting and archiving.

Online-Workshop

Wednesday, July 14, 2021
9:00 a.m. - 1:00 p.m.

Thursday, July 15, 2021
9:00 a.m. - 1:00 p.m

Trainer

Prof. Dr. Jürgen Pomp

Language

English

Location

Online

Target Group

Doctoral candidates and postdocs from all subject areas.

Track(s)

Research, Research Management

Certificate

11 units are applicable within the "Doctorate plus" certificate

Eine Wissenschaftlerin und ein Wissenschaftler arbeiten hinter einer Glasfassade und mischen Chemikalien mit Großgeräten.
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Course Content

  • GLP basics (definition, areas, laws and regulations)
  • Test facility (organisation and responsibilities)
  • Standard operating procedures and study plans
  • Conduct of GLP studies with trained staff
  • Qualification of equipment under GLP
  • Documentation and archiving
  • Excercize: Good documentation practice (Case studies)
  • Audits and inspections

Course Description

The purpose of this course is to promote the development of quality test data and provide a tool to ensure a sound approach to the management of laboratory studies, including planning, conduct, data evaluation, reporting and archiving. The GLP principles may be considered as a set of standards for ensuring the quality, reliability and integrity of studies, the reporting of verifiable conclusions and the traceability of data.

The system is regulated worldwide in different laws and regulations and builds the bridge between university research and (regulated) industrial research. The focus of these studies are the safety aspects of new compounds that will be used in our environment like chemicals, pharmaceuticals, pesticides, food additives, etc.

This set of standards include, well-trained staff, best laboratory materials, qualified equipment, validated methods and computerized systems as well as a good documentation practice.

The participants in this course will be skilled in the theoretical aspects of GLP. The course is designed for those who wish to know more about regulated industrial research. The course explores quality issues within preclinical GLP and provides an opportunity for beginners to update their competencies. In this course, both theoretical aspects and case studies of GLP are trained.

Time Table

Day 1

09:00-10:00 a.m.: GLP basics (definition, areas, laws and regulations)
10:00-11:00 a.m.: Test facility (organisation and responsibilities)

Break

11:15-12:00 a.m.: Standard operating procedures and study plans
12:00- 01:00 p.m.: Conduct of GLP studies with trained staff


Day 2

09:00-10:00 a.m.: Qualification of equipment under GLP
10:00-11:00 a.m.: Documentation and archiving

Break

11:15-12:00 a.m.: Excercize: Good documentation practice (Case studies)
12:00-01:00 p.m.: Audits and inspections

Contact

Bonn Graduate Center

Contact

+49 228 73-60141

graduiertenzentrum@uni-bonn.de

Address

Alte Sternwarte
Poppelsdorfer Allee 47
53115 Bonn

Also see

Certificate Doctorate plus

Acquire the Doctorate plus Certificate in one of our three career tracks.

Qualification Program    Doctorate plus

Expand your skills with our qualification program Doctorate plus.

Newsletter - Bonn Doctoral Bulletin

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