Those completing this course will have an understanding of the concepts and statistical methods required in biological and health science research. They will be able to interpret results related to design and analysis issues as routinely presented in the scientific literature and clinical trials. more

Included in the course content is an overview of the regulatory and pre-marketing steps that occur to ensure a successful launch. The course also covers sales planning and the commercialization decisions that affect the development of the drug. more

This is a three-day course designed to provide individuals with an in-depth understanding of the clinical research process, the roles and responsibilities of key players, as well as, regulatory requirements. The course consists of lecture and exercises. more

This course focuses on developing and implementing regulated computer systems with an appropriate level of documented evidence to satisfy FDA expectations. more

The Meetingpoint at MEDTC 2010 gives you the opportunity to meet potential cooperation partners from all over Europe.

The event will take place on Wednesday, 24 and Thursday, 25 March 2010 in the Region Stuttgart Lounge. The Enterprise Europe Network will use MEDTEC Europe as a platform for the international Medical Technology Meetingpoint 2010. The Meetingpoint will enable you to choose dialogue partners in advance of the fair via the Meetingpoint website, adding an extra dimension to your MEDTEC 2010 visit. more

The course provides a thorough understanding of the activities involved during the Phase 1 and 2 stages of Drug Development. more

50£ discount on registration fee for members of the Medical Cluster.

Call for Swiss life science companies interested in forging stronger UK-Swiss bioindustry trade links, scientific collaborations, partnerships and strategic alliances…

BioTrinity 2010 is UK's Premier Biopartnering and Investment conference and is building on its reputation as Europe's fastest growing partnering conference with more investors than any other UK conference.

Join us as we bring together a critical mass: a multitude of investors, global pharma and innovative R&D companies all within an hour of Heathrow. 35 investment firms have already confirmed participation with 3 months to go. more

The course provides a thorough understanding of the activities involved during Phase 3 and 4 of Drug Development. more

Upon completion of this course you will have a clear understanding of international regulatory authority regulations and expectations and will have gained the background knowledge necessary to effectively plan and execute QC test method validation programs. more

Course notes and interactive exercises address how to write effective correspondence and reports in support of the company’s activities. You will learn how to organize and deliver information for the intended audience. more

Insights and practical suggestions on how to develop and manage a clinical phase-dependent CMC regulatory compliance strategy for biopharmaceuticals and biologics are offered in this course. more

Die eintägige Fachveranstaltung findet am Donnerstag, 15. April in St. Gallen, Schweiz statt. Unser Partner, inspire AG, irpd institute for rapid product development hat ein äusserst interessantes Programm mit hochkarätigen Referenten zusammengestellt. Es ist uns gelungen, ausgewiesene Experten zu gewinnen, die aus Sicht der produzierenden Medizintechnikindustrie, aus Sicht der Technologieanbieter, aus Sicht der regulatorischen Zulassung sowie aus Sicht der Kliniken über die Chancen und Herausforderungen generativer Verfahren sprechen werden. more

This course presents a comprehensive overview of process writing that the binding regulations require. more

This course will provide the participant with knowledge of current GMPs, how they are applied in the Bio/Pharmaceutical market today, and how they will be enforced in the future. more

In this course QA/QC regulations and guidances from the U.S. FDA, EMEA and ICH are discussed in detail. more

This course addresses what documents you need to control, what documentation you need to support your actual system and how to keep your documents current and compliant. more

This course is intended to give participants a thorough overview and practical understanding of Current Good Manufacturing Practices for laboratory compliance. more

Upon completion of this course attendees will have a thorough knowledge of the requirements for developing and marketing Medical Devices in the European Union. more

This course provides an overview of how to present product information clearly and concisely for the targeted audience. Hands-on exercises reinforce the course content. more

This course focuses on understanding the requirements of the new EU Clinical Trial Directive and the issues inherent in any new regulatory process. more

The course will provide the tools needed to prepare for a Clinical Data System inspection and to assess risk areas that need prioritization. more

The course will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies in the EU and individual European countries. more

Im Bereich Entwicklung und Anwendung von Gehörhilfen braucht es spezifisches Wissen über Akustik, die Funktionsweise des Gehörs und die technischen Möglichkeiten zur Vermeidung oder Behandlung von Hörstörungen. Das CAS Akustik und Audiologie vermittelt die dazu nötigen medizinischen, technischen und regulatorischen Grundlagen und Anwendungskenntnisse. more

Der Zertifikatskurs Grundlagen der Informatik vermittelt ein Verständnis für die grundlegenden Konzepte und Einsatzmöglichkeiten der modernen Informatiktechnologien. more

Dieser Kurs behandelt die besonderen Aspekte von Beschaffung und Verkauf in der Medizintechnik anhand eines Übungsbeispiels (Living Case) für die Beschaffung eines Computertomographen.

Er besteht aus drei Teilkursen (Beschaffung und Verkauf, Bildgebung, Medizinische Grundlagen), die auch einzeln belegt werden können. more

Dieser Kurs vermittelt die besonderen Aspekte von Beschaffung und Verkauf in der Medizininformatik anhand eines Übungsbeispiels (Living Case) für RIS/PACS-Systeme. Er besteht aus drei Teilkursen (Beschaffung und Verkauf, Bildgebung, Medizinische Grundlagen), die auch einzeln belegt werden können. more

Dieser Kurs vermittelt ein Spektrum an medizinischen Grundlagen im Bereich der menschlichen Physiologie, Anatomie und der Beschwerdebilder.

Der Kurs behandelt die Grundlagen in Anatomie, Pathologie, Physiologie und Pathophysiologie, so dass die häufigsten Krankheiten verstanden werden können. Weiter vermittelt der Kurs die Grundmechanismen
der Molekularbiologie und der körperlichen Abwehr von Krankheitserregern wie Viren, Bakterien und Pilzen. more

The 2010 SSB Annual Meeting and General Assembly will take place at the Empa Academy in Dübendorf on May 5, 2010.

The topic of the meeting will be Biomaterials and Tissue Engineering. more

After completion of this course the attendee will have a strong understanding of the principles and practices of Project Management. more

Wie können wir den Wettbewerbsfaktor Gesundheit optimaler in unserem Unternehmen einsetzen?

• Welches sind mögliche Bausteine im Gesundheits-Management?
• Wer trägt die Verantwortung für die Gesundheit im Unternehmen?
• Was muss ich beachten?
• Wie erreiche ich das Wohlfühlklima im Unternehmen?

The primary objective of this course is to develop an understanding of the principles and techniques involved in the practice of Root Cause Analysis. more

Die Tagung bietet Fachpersonen aus dem Bereich Implantate eine Plattform zum Informations- und Erfahrungsaustausch. Der thematische Fokus liegt bei aktuellen Fragen und Problemen zu Werkstoffen, Oberflächen und Prozessen bei inaktiven, medizinischen Implantaten. Mit dem Seminar sprechen wir Hersteller, Zuliefer-unternehmen, Anwender und Dienstleistungsunternehmen an, die sich mit dem Thema befassen. Das Tagungsprogramm beinhaltet Expertenvorträge (invited lectures), freie Vorträge sowie genügend Raum für individuelle Gespräche und Networking. more

The objective of this course is to provide an overview of the preparation, design and management aspects of clinical trials for medical devices. more

This course is specifically focused on the law, regulations and policies set down by the FDA for the manufacture of medical devices. more

The purpose of this course is to provide an introduction to the fundamentals of process validation, explaining how, when, where and why you should validate. more

EuroMedtech™ is Europe's leading medical technology partnering conference, providing collaboration opportunities to medtech decision makers and investors. EuroMedtech caters for companies involved in all parts of the advanced medical technology industry, from those serving mainline therapeutic categories such as orthopedics and cardiovascular, through diagnostics, imaging and telemedicine to those involved in platform technologies such as biomaterials and regenerative medicine. Also attending are companies serving the industry, such as manufacturers, law firms, CROs and distributors. more

Dieser Kurs vermittelt die Entwicklungsschritte für medizintechnische Produkte — von der Anforderungen bis zur Validierung— anhand eines Übungsbeispiels (Living Case) aus der Technik für Hörhilfen. Er besteht
aus drei Teilkursen (V-Modell, Cochlear Implantate und Medizinische Grundlagen), die auch einzeln belegt werden können. more

Dieser Kurs vermittelt die Entwicklungsschritte — von der Anforderungen bis zur Validierung — anhand eines Übungsbeispiels (Living Case) aus dem Bereich Praxisinformationssysteme. Er besteht aus drei Teilkursen (Requirement & System Engineering, Medizininformatik und Medizinische Grundlagen), die auch einzeln belegt werden können. more

Context:
The development of new products/devices/medicines is a very long process. A thorough planning of the different steps/milestones of the project is key for a long term success.

Objectives:
To assess the key success factors for a project and to master its planning. To learn how to give a project solid foundations and precise objectives; to address project risk management. more

Die 2. Fachtagung KUNSTSTOFFE MEDICAL SWISS - Plastics and Cardiovascular - am 08. Juni 2010 in Luzern informiert Sie über bestehende Einsatzgebiete, zusätzliche Potenziale und aktuelle Trends.
Im Anschluss an die Vorträge werden die Herausforderugen in der In-Virto-Diagnostik in einer hochkarätigen Diskussionsrunde erörtert.
more

Join the Swiss Pavliion!

Medica is considered to be the most important world exhibition of medical technology. MEDICA presents a remarkable portfolio of products, topics and companies, from innovative small businesses to  medium-sized companies and even global players. Numerous countries regularly exhibit the products of their enterprises on their respective national pavilions. In 2009, the most recent developments and materials of more than 4’300 exhibitors from more than 60 countries have taken up a surface on 20 halls. The number of visitors coming from 100 countries totalled 137’000. more