FORUM Institut für Management GmbH: 83 Produkte
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…
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…
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…
e-Learning: Managing Director - Duties and Liabilities in a German "GmbH"
Die Themen - Introduction - the (legal) position of the managing director - The fundamental rights and duties - Liability against the GmbH,…
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…
e-Learning: German Accounting Basics
Die Themen - Basic Accounting Principles - Accounting for Intangible Assets - Basics of Group Accounting - Accounting for Provisions and Co…
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…
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…
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…
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…
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…
e-Learning: Auditing EU Funds: Essential Principles for Beginners
Die Themen - Legal framework at EU level - Overall assurance and multi-annual audit strategy - Different types of audits - Thematic audits …
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…
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…
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…
