| Date | Title | Category |
Speaker
All Christian Rosenzweig Dipl.-Ing Sven Wittorf Dirk Bethäußer Lea Wettlaufer Mario Klessascheck Matthias Hölzer-Klüpfel Prof. Dr. Oliver Haase Thomas Geis Ulrich Hafen Dr. Nadine Jurrmann Urs Müller Andreas Kalchschmid-Lehmann Margret Seidenfaden Dr. Bernhard Gerstenecker Katharina Keutgen Dr. Manuela Reinhold Claudia Volk Claudia Schmitt Anja Kuhnert Dr.-Ing. Philipp Schleer Dr. Tanja Domke Dipl.-Ing. Sarah Gruber Robert Dick-Hambeck Prof. Dr. rer. nat. Daniel Mertens Dr. Sophie Bartsch Dr.-Ing. Thimo Keller Dr.-Ing. Christopher Stockinger Katrin Schnetter Prof. Dr. Christian Johner Dr. Daniel Mölle Dr. Andreas Thiel Dr. Tina Priewasser M.Sc. Philipp Koppenhagen Dimitrios-Karolos Kaloulis M.Sc. |
Location
All |
Language
All |
Price
(plus VAT)
|
Seats available | Registration |
|---|---|---|---|---|---|---|---|---|
|
17.11.2026
|
Regulatory Basics (MDR) |
Dr. Nadine Jurrmann Anja Kuhnert |
German |
880
|
|
|||
|
17.11.2026
|
Workshop "AI Power Advanced: LLM Mastery for Medical Device Manufacturers" |
AI & Digital Technologies |
Mario Klessascheck |
German |
1280
|
|
||
|
19.11.2026
|
PRRC & Authorized Representatives |
Dr. Manuela Reinhold |
German |
450
|
|
Booked out |
||
|
24.11
-
25.11.2026 |
Medical Software & IT Security |
Christian Rosenzweig |
German |
1600
|
|
|||
|
24.11
-
25.11.2026 |
Clinical Evaluation & Literature Research |
Susanne Golombek Anja Kuhnert |
German |
680
|
|
|||
|
25.11.2026
|
Quality Management, Auditing, & Risk Management |
Katrin Schnetter |
German |
390
|
|
|||
|
25.11.2026
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
390
|
|
|||
|
25.11.2026
|
Practical Workshop "AI Power for Medical Device Development" |
AI & Digital Technologies |
Mario Klessascheck |
German |
1280
|
|
||
|
30.11
-
03.12.2026 |
Seminar "Certified Professional for Medical Software (CPMS)" |
Medical Software & IT Security |
Matthias Hölzer-Klüpfel Dipl.-Ing Sven Wittorf |
German |
3320
|
|
||
|
01.12
-
02.12.2026 |
Medical Software & IT Security |
Claudia Schmitt |
German |
880
|
|
|||
|
02.12
-
03.12.2026 |
Quality Management, Auditing, & Risk Management |
Christian Rosenzweig |
German |
1600
|
|
|||
|
09.12.2026
|
Medical Software & IT Security |
Dipl.-Ing Sven Wittorf |
German |
680
|
|
|||
|
09.12
-
10.12.2026 |
Seminar Internal Auditor Medical Devices according to ISO 19011 |
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
1360
|
|
||
|
15.12.2026
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
680
|
|
|||
|
26.01.2027
|
PRRC & Authorized Representatives |
Dr. Manuela Reinhold |
German |
390
|
|
|||
|
16.02.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
680
|
|
|||
|
16.02
-
17.02.2027 |
Seminar Person Responsible for Regulatory Compliance according to Article 15 MDR |
PRRC & Authorized Representatives |
Margarita Rozhdestvenskaya |
German |
680
|
|
||
|
17.02
-
18.02.2027 |
Quality Management, Auditing, & Risk Management |
Claudia Schmitt |
German |
1360
|
|
|||
|
23.02.2027
|
In-vitro Diagnostic Medical Devices & IVDR |
Ulrich Hafen |
German |
680
|
|
|||
|
23.02.2027
|
Seminar Regulatory Requirements for Distributors and Importers |
Regulatory Basics (MDR) |
Dr. Manuela Reinhold |
German |
390
|
|
||
|
24.02.2027
|
AI & Digital Technologies |
M.Eng. Anja Bentz |
German |
780
|
|
|||
|
24.02
-
25.02.2027 |
Medical Software & IT Security |
Claudia Schmitt |
German |
780
|
|
|||
|
09.03
-
10.03.2027 |
Product Safety |
Mario Klessascheck |
German |
1560
|
|
|||
|
10.03
-
11.03.2027 |
Product Safety |
Dr. Andreas Thiel |
German |
680
|
|
|||
|
11.03.2027
|
Medical Software & IT Security |
Katrin Schnetter |
German |
680
|
|
|||
|
11.03.2027
|
Regulatory Basics (MDR) |
Dr. Nadine Jurrmann Anja Kuhnert |
German |
880
|
|
|||
|
15.03
-
18.03.2027 |
Seminar "Certified Professional for Medical Software (CPMS)" |
Medical Software & IT Security |
Matthias Hölzer-Klüpfel Dipl.-Ing Sven Wittorf |
German |
3320
|
|
||
|
16.03.2027
|
Workshop Mastering structured data – for medical technology manufacturers and notified bodies |
AI & Digital Technologies |
M.Sc. Philipp Koppenhagen |
German |
780
|
|
||
|
16.03
-
17.03.2027 |
Seminar Internal Auditor Medical Devices according to ISO 19011 |
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
1360
|
|
||
|
16.03
-
17.03.2027 |
Clinical Evaluation & Literature Research |
Susanne Golombek Anja Kuhnert |
German |
680
|
|
|||
|
17.03
-
18.03.2027 |
Usability & Requirement Engineering |
Thomas Geis |
German |
1480
|
|
|||
|
18.03.2027
|
PRRC & Authorized Representatives |
Dr. Manuela Reinhold |
German |
390
|
|
|||
|
06.04.2027
|
Regulatory Basics (MDR) |
Dr. Manuela Reinhold |
German |
680
|
|
|||
|
06.04.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
390
|
|
|||
|
08.04.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
680
|
|
|||
|
13.04.2027
|
Quality Management, Auditing, & Risk Management |
Ulrich Hafen |
German |
680
|
|
|||
|
15.04.2027
|
Practical Workshop AI Power for Medical Device Development and approval |
AI & Digital Technologies |
Mario Klessascheck |
German |
1280
|
|
||
|
20.04.2027
|
Regulatory Requirements for AI-Based Medical Devices and IVDs |
AI & Digital Technologies |
M.Eng. Anja Bentz Dr. Tina Priewasser |
German |
780
|
|
||
|
20.04
-
21.04.2027 |
Clinical Evaluation & Literature Research |
Dr. Nadine Jurrmann |
German |
680
|
|
|||
|
20.04
-
28.04.2027 |
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
3600
|
|
|||
|
27.04
-
28.04.2027 |
Quality Management, Auditing, & Risk Management |
Claudia Schmitt |
German |
1360
|
|
|||
|
27.04
-
28.04.2027 |
Practical Workshop AI Power for medical device development ans approval (two afternoons) |
English Seminars |
Mario Klessascheck |
English |
1280
|
|
||
|
28.04.2027
|
Quality Management, Auditing, & Risk Management |
Katrin Schnetter |
German |
680
|
|
|||
|
04.05
-
05.05.2027 |
Seminar Person Responsible for Regulatory Compliance according to Article 15 MDR |
PRRC & Authorized Representatives |
Margarita Rozhdestvenskaya |
German |
680
|
|
||
|
11.05.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
680
|
|
|||
|
12.05.2027
|
PRRC & Authorized Representatives |
Dr. Manuela Reinhold |
German |
390
|
|
|||
|
12.05
-
13.05.2027 |
Seminar Internal Auditor Medical Devices according to ISO 19011 |
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
1360
|
|
||
|
12.05
-
13.05.2027 |
In-vitro Diagnostic Medical Devices & IVDR |
Dr. Sophie Bartsch |
German |
680
|
|
|||
|
13.05.2027
|
In-vitro Diagnostic Medical Devices & IVDR |
Dr. Juliane Havlicek |
German |
680
|
|
|||
|
08.06.2027
|
Product Safety |
Mario Klessascheck |
German |
780
|
|
|||
|
10.06.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
390
|
|
|||
|
10.06.2027
|
In-vitro Diagnostic Medical Devices & IVDR |
Dr. Sophie Bartsch |
German |
490
|
|
|||
|
15.06.2027
|
Workshop Mastering structured data – for medical technology manufacturers and notified bodies |
AI & Digital Technologies |
M.Sc. Philipp Koppenhagen |
German |
780
|
|
||
|
15.06
-
16.06.2027 |
Clinical Evaluation & Literature Research |
Susanne Golombek Anja Kuhnert |
German |
680
|
|
|||
|
15.06
-
16.06.2027 |
Medical Software & IT Security |
Claudia Schmitt |
German |
780
|
|
|||
|
16.06.2027
|
Medical Software & IT Security |
Katrin Schnetter |
German |
680
|
|
|||
|
17.06.2027
|
In-vitro Diagnostic Medical Devices & IVDR |
Ulrich Hafen |
German |
680
|
|
|||
|
22.06.2027
|
Regulatory Basics (MDR) |
Dr. Manuela Reinhold |
German |
680
|
|
|||
|
23.06.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
680
|
|
|||
|
29.06.2027
|
AI & Digital Technologies |
M.Eng. Anja Bentz |
German |
780
|
|
|||
|
30.06
-
01.07.2027 |
Quality Management, Auditing, & Risk Management |
Claudia Schmitt |
German |
1360
|
|
|||
|
01.07.2027
|
PRRC & Authorized Representatives |
Dr. Manuela Reinhold |
German |
390
|
|
|||
|
06.07.2027
|
Seminar Regulatory Requirements for Distributors and Importers |
Regulatory Basics (MDR) |
Dr. Manuela Reinhold |
German |
390
|
|
||
|
12.08.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
680
|
|
|||
|
17.08
-
18.08.2027 |
Seminar Internal Auditor Medical Devices according to ISO 19011 |
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
1360
|
|
||
|
24.08.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
390
|
|
|||
|
14.09.2027
|
Regulatory Basics (MDR) |
Dr. Nadine Jurrmann Anja Kuhnert |
German |
880
|
|
|||
|
14.09
-
15.09.2027 |
Medical Software & IT Security |
Claudia Schmitt |
German |
780
|
|
|||
|
15.09.2027
|
PRRC & Authorized Representatives |
Dr. Manuela Reinhold |
German |
390
|
|
|||
|
15.09
-
16.09.2027 |
Seminar Person Responsible for Regulatory Compliance according to Article 15 MDR |
PRRC & Authorized Representatives |
Margarita Rozhdestvenskaya |
German |
680
|
|
||
|
20.09
-
23.09.2027 |
Medical Software & IT Security |
Matthias Hölzer-Klüpfel Dipl.-Ing Sven Wittorf |
German |
3320
|
|
|||
|
21.09
-
22.09.2027 |
Quality Management, Auditing, & Risk Management |
Claudia Schmitt |
German |
1360
|
|
|||
|
21.09
-
22.09.2027 |
Usability & Requirement Engineering |
Thomas Geis |
German |
1480
|
|
|||
|
22.09
-
23.09.2027 |
Clinical Evaluation & Literature Research |
Dr. Nadine Jurrmann |
German |
680
|
|
|||
|
22.09
-
23.09.2027 |
Regulatory Basics (MDR) |
Dr. Manuela Reinhold |
Frankfurt |
German |
1560
|
|
||
|
23.09.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
680
|
|
|||
|
23.09.2027
|
Regulatory Requirements for AI-Based Medical Devices and IVDs |
AI & Digital Technologies |
M.Eng. Anja Bentz Dr. Tina Priewasser |
German |
780
|
|
||
|
30.09.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
390
|
|
|||
|
07.10.2027
|
AI & Digital Technologies |
M.Eng. Anja Bentz |
German |
780
|
|
|||
|
19.10.2027
|
Regulatory Basics (MDR) |
Dr. Manuela Reinhold |
German |
680
|
|
|||
|
19.10
-
20.10.2027 |
Seminar Internal Auditor Medical Devices according to ISO 19011 |
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
1360
|
|
||
|
19.10
-
20.10.2027 |
Product Safety |
Dr. Andreas Thiel |
German |
680
|
|
|||
|
20.10
-
21.10.2027 |
Product Safety |
Mario Klessascheck |
German |
1560
|
|
|||
|
21.10.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
680
|
|
|||
|
25.10
-
28.10.2027 |
CPMS - Certified Professional for Medical Software (English) |
English Seminars |
Matthias Hölzer-Klüpfel Dipl.-Ing Sven Wittorf |
English |
3320
|
|
||
|
26.10
-
04.11.2027 |
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
3600
|
|
|||
|
27.10.2027
|
In-vitro Diagnostic Medical Devices & IVDR |
Ulrich Hafen |
German |
680
|
|
|||
|
09.11
-
10.11.2027 |
In-vitro Diagnostic Medical Devices & IVDR |
Dr. Sophie Bartsch |
German |
680
|
|
|||
|
09.11
-
10.11.2027 |
IEC 60601-1 Medical Electrical Equipment Safety Seminar (English) two days |
English Seminars |
Mario Klessascheck |
English |
1560
|
|
||
|
10.11.2027
|
Quality Management, Auditing, & Risk Management |
Katrin Schnetter |
German |
680
|
|
|||
|
10.11
-
11.11.2027 |
Clinical Evaluation & Literature Research |
Susanne Golombek Anja Kuhnert |
German |
680
|
|
|||
|
11.11.2027
|
Quality Management, Auditing, & Risk Management |
Ulrich Hafen |
German |
680
|
|
|||
|
11.11.2027
|
Seminar Regulatory Requirements for Distributors and Importers |
Regulatory Basics (MDR) |
Dr. Manuela Reinhold |
German |
390
|
|
||
|
11.11
-
12.11.2027 |
Seminar Person Responsible for Regulatory Compliance according to Article 15 MDR |
PRRC & Authorized Representatives |
Margarita Rozhdestvenskaya |
German |
680
|
|
||
|
16.11.2027
|
Workshop Mastering structured data – for medical technology manufacturers and notified bodies |
AI & Digital Technologies |
M.Sc. Philipp Koppenhagen |
German |
780
|
|
||
|
18.11.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
390
|
|
|||
|
24.11.2027
|
Regulatory Requirements for AI-Based Medical Devices and IVDs |
English Seminars |
M.Eng. Anja Bentz Dr. Tina Priewasser |
English |
780
|
|
||
|
24.11
-
25.11.2027 |
Quality Management, Auditing, & Risk Management |
Claudia Schmitt |
German |
1360
|
|
|||
|
25.11.2027
|
PRRC & Authorized Representatives |
Dr. Manuela Reinhold |
German |
390
|
|
|||
|
30.11.2027
|
Medical Software & IT Security |
Katrin Schnetter |
German |
680
|
|
|||
|
01.12
-
02.12.2027 |
Medical Software & IT Security |
Claudia Schmitt |
German |
780
|
|
|||
|
02.12.2027
|
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
680
|
|
|||
|
07.12.2027
|
Regulatory Basics (MDR) |
Dr. Manuela Reinhold |
German |
680
|
|
|||
|
14.12
-
15.12.2027 |
Seminar Internal Auditor Medical Devices according to ISO 19011 |
Quality Management, Auditing, & Risk Management |
Dirk Bethäußer |
German |
1360
|
|
In some situations, booking one of our seminars in-house may be useful. All of our seminars can also be customized as in-house seminars. Depending on your needs, these can be held online or at your premises.
We particularly recommend an in-house seminar if you:
Get in touch with us right away to request a suitable in-house seminar.
Phone
+49 7531 94500 20
Contact Form