Gläsernes Labor Akademie
+49 (0) 30 94 89 29 35
Good Clinical Practice (GCP) is the ethical and scientific basis for the planning, preparation, conduct and reporting of clinical trials. GCP defines the principles for any clinical trial conducted with medicinal products. GCP has been introduced by ICH (International Council on Harmonization) in 1997 and was just recently revised.
The seminar will include presentations with a lot of practical examples as well as workshops on the most important topics of GCP. The trainer will focus on the responsibilities of the study sponsor (e.g. pharmaceutical or biotech company) but will also cover those elements that are of importance for the investigational team at the study site, i.e. at the hospital or private practice.
According to local law (§ 11 Berliner Bildungsurlaubsgesetzes BiUrlG) educational leave applies.
History and development of GCP; differentiation between clinical trial and non-interventional study; responsibilities of study sponsors including risk-based approach, quality management (quality assurance and quality control); responsibilities of the investigator in practical terms; submission to ethics committees and competent authorities; preparation, conduct and reporting of a clinical trial with medicinal products.
The qualification will comprise a total of 8 lessons which will be held on Thursday, 06 Jun 19 from 9:00 a.m. till 05.00 p.m.
The course will be held with a minimum of 6 and a maximum of 16 attendees. Due to organization alreasons, an early registration is recommended.
The course is directed
After course completion, attendees will have developed a basic understanding of GCP requirements for the planning, preparation and conduct of clinical trials with medicinal products. Thus, based on their individual background, also participating academic researchers should be able to identify potential occupational fields in the industry dealing with GCP topics.
The successful participation will be certified by the Gläsernes Labor Akademie (GLA).
Dr. Christoph Ortland has a 25 years’ experience in the development of medicinal products and medical devices. He held different positions in industry before starting to work self-employed in the beginning of 2011. In 2017, Christoph founded the Clinical Research Organization “Forschungsdock GmbH”, which is located near Hamburg and supports studysponsors in all aspects of clinical trials and studies. He is an experienced project manager, monitor, auditor and trainer.
589,00 € per participant incl. VAT (495,00 EUR excl. VAT).
Private registrees will get a fee reduction of about 10%.