FORUM Institut für Management GmbH: 83 Produkte
Pharmacovigilance Auditing - Planning and conducting GVP Audits
Die Themen - Qualifications and responsibilities according to GVP Module IV - Conducting effective interviews - Auditing of PV documents, c…
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…
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…
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…
e-Learning: Working with the Works Council in Germany
Die Themen - Legal framework, main principle, formation and types of the works council - Legal position of the works council and of its mem…
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: 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…
Medical Devices for Beginners - Compact seminar on the entire medical device development process in compliance with the MDR
Die Themen - Introduction to medical devices and regulatory fundamentals - Classification and conformity assessment procedures - Clinical e…
e-Learning: AMNOG briefly and concisely - Learn AMNOG in 5 Modules: From Concept and Data Requirements to the Full Process
Die Themen - Benefit Assessment: HTA in Europe, AMNOG in Germany - Benefit Assessment according to § 35a SGB V - a Quick Overview - The Str…
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…
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,…
e-Learning: Medical Devices Basics - A Quick Introduction - E-learning with 3 modules: Medical Device Law, Development and Conformity Asses…
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: 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…
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…
