FORUM Institut für Management GmbH: 38 Produkte
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…
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…
CMC for Biologicals - With a focus on proteins
Die Themen - Regulatory framework: ICH guidelines (including an outlook on the new (Draft) ICH Q1 and ICH M4Q(R2)) - Essential data for bio…
Advanced Class: The Global Network of Local and Regional QPPVs - Global Collaboration and Inspection Readiness
Die Themen - Responsibilities and collaboration between QPPVs and National Safety Officers - Overview: Country-specific regulatory requirem…
EU Regulatory Strategy - From Development to Approval - Strategic Planning in a Changing EU Framework
Die Themen - Strategic position of regulatory affairs within your organisation - Cross-functional collaboration with R&D, PV, market access…
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…
Global CMC requirements: focus on Asia, Japan, and Eastern Europe - Covering aspects for small and large molecules
Die Themen - Regions covered: China, Japan, South Korea, India, Russia/EAEU - Pharmaceutical legislation - Additions and differences with r…
Invent with AI Masterclass
Die Themen - Impact of integrating AI into the patent portfolio management process on an organization's innovation and IP strategy - Use of…
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 …
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…
Amsterdam Masterclass: EPO Oppositions & Appeals - Best Practices on the Proceedings on 1.5 Days
Die Themen - Opposition Proceedings in the light of RPBA: drafting notice of opposition anticipating admissibility hurdles, substantive exa…
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…
How to Protect And Manage Trade Secret Assets
Die Themen - Evolving developments shaping the trade secret landscape - Disputes and enforcement - Why trade secret metadata matters - Less…
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…
Leveraging AI in Evidence Generation and Market Access
Die Themen - Dossier Writing - Use cases for AI support - Using AI in Systematic Literature Review (SLR) - LLMs for describing and evaluati…
