FORUM Institut für Management GmbH: 83 Produkte
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…
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…
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 …
Global Pharmacovigilance Inspection Readiness - Strategies for successful PV (remote) inspections in Germany, Europe and worldwide
Die Themen - Fundamentals: regulations, occurrence, types and aims - Strategic planning and preparation for a (remote) GVP inspection - Rep…
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…
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…
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…
Webcast: Update EU Pharma Legislation - Clear guidance on upcoming EU requirements in a five-module webcast series
Die Themen - Module 1: The legal framework part 1 - overview and current procedural status - Module 2: The legal framework part 2 - protect…
Pharmaceutical Marketing Authorisation and Market Access in the Middle East: GCC and National Markets - Connect with regional experts from …
Die Themen - Pharmaceutical marketing authorisation and market access in the GCC and key national markets - Intellectual property: Patents,…
Variations in Europe - Practical Guidance on Classification, Submission and Current Regulatory Updates
Die Themen - Variation Regulation (inlcuding new features since 01.01.25) - Classification and submission (including new features since 15.…
e-Learning: Leading agile and resilient teams - Coaching Strategies to climb mountains
Die Themen - Coaching strategies to facilitate positive outcomes - How to ensure high level of team performance - Effective coaching questi…
Abonnement: PharmaFORUM Webcast International - "Electronic Product Information (ePI): Global Developments and Regulatory Perspectives" 12 …
Die Themen - The evolving complexity of CMC documentation in global submissions - Regulatory Intelligence in a Global Context - Regulatory …
