FORUM Institut für Management GmbH: 83 Produkte
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…
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…
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…
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…
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…
2nd AI & IP FORUM - In-Person Conference for Important Updates and Expert Discussions on Artificial Intelligence and Intellectual Property
Die Themen - Use of AI at patent offices for search, examination, opposition and appeals - Use of AI in IP departments: use cases and succe…
