FORUM Institut für Management GmbH: 60 Produkte
WIR BILDEN WEITER - 40 Jahre FORUM Institut.
Wir unterstützen seit 40 Jahren Fach- und Führungskräfte nahezu aller Unternehmensbereiche, indem wir wichtige Trends und notwendiges Fachwissen erkennen, aufbereiten und in angenehmer Atmosphäre vermitteln.
Unterschiedliche Projektbereiche konzipieren Konferenzen, Seminare, Lehrgänge, Workshops und e-Learnings für viele industrielle Branchen und Wirt…
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Webcast series: Global regulatory requirements for drug device combination products (DDCs) - Overview for the EU, US, China, and MENA region
Die Themen - Concept: Four weekly live webcasts à 3/2 hours with longtime experienced speakers - Regions covered: EU, US, China, and MENA r…
€ 1.725,50 inkl. MwSt. Max.: 1564 Tage
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e-Learning: Medical Device Advisor §83 MPDG - e-Learning in 5 modules for non-German speaking employees
Die Themen - European Medical Device Law and its Application in Germany - Definition of a medical device is and how it is brought to market…
€ 464,10 inkl. MwSt. Max.: 2001 Tag
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Clinical Trial Project Management - Skills, Tools, and Methods for Successful Clinical Drug Trials
Die Themen - Project management - tools, plans & documentation - Managing the "people-business" - skills and methods - Setting up a project…
€ 2.368,10 inkl. MwSt. Max.: 152 Tage
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Supervisory Board Members in German Financial Institutions - Fit & Proper, regulatory & liability framework
Die Themen - Regulatory framework for financial institutions - Responsibilities, duties of members of Supervisory Board - Fit & Proper - Re…
€ 856,80 inkl. MwSt. Max.: 51 Tag
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SPC 2026: The Supplementary Protection Certificates Update - EU Reform And Case-Law
Die Themen - Key issues of the Supplementary Protection Certificates - SPC reform, e.g. unitary SPC - ECJ referrals from Medeva to Teva v M…
Max.: 152 Tage
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Biopharmaceuticals - Development, manufacturing and analytics of monoclonal antibodies and other proteins
Die Themen Development & manufacturing on 8 June 2026: - Manufacturing process - Formulation - Process changes Regulatory requirements on 9…
Max.: 153 Tage
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Quality Management and Process Optimization in Medical Affairs - Structuring business processes, ensuring quality documentation and complia…
Die Themen - Compliance & Business Process Management (BPM) in Medical Affairs - Business Process Management & Quality Documentation in Med…
€ 1.535,10 inkl. MwSt. Max.: 201 Tag
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Successful Business Negotiation - Strategies and Tools for Better Deals and Agreements
Die Themen - Mastering the Art of Negotiation: From Strategy to Successful Execution - Effective Negotiation Preparation: Step-by-Step to a…
€ 1.416,10 inkl. MwSt. Max.: 151 Tag
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Regulatory Lifecycle Management - Maintenance and sustainment of human medicinal product approvals
Die Themen - Time and deadline management in the product lifecycle - Internal company interactions and coordination - Variations system and…
€ 1.535,10 inkl. MwSt. Max.: 151 Tag
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CMC Management in Regulatory Affairs - Quality data for marketing authorisation in Europe
Die Themen - Regulatory requirements in the EU and the ICH region - Update on the new (Draft) ICH M4Q(R2) - Essential quality data for mark…
€ 2.368,10 inkl. MwSt. Max.: 152 Tage
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ExpertFORUM Global Regulatory Affairs - Trends and Strategies
Die Themen - Joint Scientific Consultation and global evidence planning - Reliance pathways: ACCESS, ORBIS, OPEN - Strategic real-world evi…
€ 1.892,10 inkl. MwSt. Max.: 202 Tage
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e-Learning: GDP - Basic Training - Basic training to understand the requirements of GDP in today's pharmaceutical industry
Die Themen - Defining GDP - From regulations to implementation: quality management - Key roles in the GDP environment - GDP in practice: st…
€ 583,10 inkl. MwSt. Max.: 11 Tag
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e-Learning: EU Variation System and Procedures - Classification, Grouping, Worksharing & Submission
Die Themen - Module 1: Overview of the EU law and Guidelines - including Commission Delegated Regulation (EU) 2024/1701 - Module 2: Classif…
€ 583,10 inkl. MwSt. Max.: 11 Tag
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Generative AI Workshop for Patent Practitioners
Die Themen - The potential of generative AI for daily patent work - Generative AI for the drafting of patent applications - The application…
€ 1.535,10 inkl. MwSt. Max.: 101 Tag
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Regulatory Affairs and GMP compliance in Eastern Europe - Considerations for the EAEU and Non-EAEU markets
Die Themen - Regulatory Framework and Requirements - Approval Processes and Documentation - Product Management and Maintenance - Quality Ma…
€ 2.368,10 inkl. MwSt. Max.: 152 Tage