the 107 Veranstaltungen

PREFERRED

U.S. Patent Formalities - The Guide to the Formal Requirements

FORUM Institut für Management GmbH (147)

- What are relevant law, rules and guidelines? - Useful USPTO resources, including Patent Center and Global Dossier - Requirements and formal documents for a U.S. patent application - Workshop: Example filing of patent application, documents and amen...

• Webinar
• Ohne Einstufung

• 02.07.2024

PREFERRED

Managing the Recovery and Resilience Funds - Lessons Learned and the Way Forward

FORUM Institut für Management GmbH (147)

- Revision plans - Do no significant harm - RRF mandates - Data on beneficial ownership - Synergies and complementarities between RRF and Cohesion Policy - Audit and control in the RRF - implications beyond 2026 The EUs Recovery and Resilience Facili...

• Seminar / Kurs
• Ohne Einstufung

• 16.05.2024 - 17.05.2024, Heidelberg (DE)

PREFERRED

The Management of Patent Portfolios

FORUM Institut für Management GmbH (147)

- Developing strategic approaches for patent portfolio optimization - Financial planning and resource allocation for patent portfolios - Structuring and coordinating patent portfolios for optimal management - Maintaining high standards in patent port...

• Webinar
• Ohne Einstufung

• 11.06.2024
• weiterer Termin verfügbar

PREFERRED

The UPC Case Management System for Paralegals

FORUM Institut für Management GmbH (147)

- Using the CMS: managing accounts, authentication, roles, representatives, and teams; Opt-out - Managing infringement and revocation proceedings, appeals and related proceedings - Dealing with the court: dates, documents, payments, languages - Case...

• Webinar
• Ohne Einstufung

• 13.05.2024 - 14.05.2024

PREFERRED

The basics of auditing EU Funds

FORUM Institut für Management GmbH (147)

- EU regulatory framework - Different types of audits and their scope - Thematic audits - IT systems and databases - Output of the work of the Audit Authority and cooperation with other authorities Wondering how to navigate the complexities of EU Fu...

• Webinar
• Ohne Einstufung

• 19.09.2024

PREFERRED

The UPC Case Management System for European Patent Litigators

FORUM Institut für Management GmbH (147)

- Using the CMS: managing accounts, authentication, roles, representatives, and teams; Opt-out - Managing infringement and revocation proceedings, appeals and related proceedings - Dealing with the court: dates, documents, payments, languages - Case...

• Webinar
• Ohne Einstufung

• 10.06.2024 - 11.06.2024

PREFERRED

PharmaFORUM Webcast International - Marketing Authorization in the USA 5 November 2024

FORUM Institut für Management GmbH (147)

Our global and local experts will update you every two months with the latest regulatory and legislative developments. Thus, you will always have the essential information and trends in regulatory affairs at your fingertips!

• Webinar
• Ohne Einstufung

• 01.11.2024 - 31.10.2025

PREFERRED

Design Protection in the European Union - A One-Day Practitioners Guide

FORUM Institut für Management GmbH (147)

- Key issues regarding the Community Designs - Application and invalidity proceedings before the EUIPO - Infringement and defences to infringement - Remedies and jurisdiction - CJEU case-law update - Case study: Papierfabriek Doetinchem Our speakers...

• Webinar
• Ohne Einstufung

• 08.10.2024

PREFERRED

The IP Strategist - Toward proactive and aligned management of innovation and IP

FORUM Institut für Management GmbH (147)

- Explore further the matrix-approach for strategy making, with advanced techniques (using Excel) - Learn new methodology to (re)align the IP portfolio with the business focus. Link IP to financials and business strategy. - Apply and present these tw...

• Seminar / Kurs
• Ohne Einstufung

• 10.06.2024 - 12.06.2024, München (DE)

PREFERRED

Advanced PCT Formalities Summer Course - Goal-oriented Guide to the Formal Requirements

FORUM Institut für Management GmbH (147)

- Influencing procedure with formality actions - Avoiding filing defects, reducing administration during national phases and problems during search and examination - Improving quality and speed of patentability opinions - Increasing value of applicat...

• Webinar
• Ohne Einstufung

• 11.07.2024 - 12.07.2024

PREFERRED

Patent Due Diligence - Learn the dos and donts of a patent due diligence

FORUM Institut für Management GmbH (147)

- Key issues in a patent due diligence - Process, milestones and strategies - Evaluating a patent due diligence: due diligence reports, typical risks, how to minimise the risks - IP provisions in acquisition contracts - Dos and donts in a patent due...

• Webinar
• Ohne Einstufung

• 14.05.2024

PREFERRED

Amsterdam Masterclass: EPO Oppositions & Appeals - Best Practices on the Proceedings on 1.5 Days

FORUM Institut für Management GmbH (147)

- Opposition Proceedings in the light of RPBA 2020: drafting notice of opposition anticipating admissibility hurdles, substantive examination, burden of proof - Oral proceedings, taking of evidence, amendments of the patent - Appeal Proceedings: impo...

• Seminar / Kurs
• Ohne Einstufung

• 13.06.2024 - 14.06.2024, Amsterdam (NL)

PREFERRED

RMP and PSUR in lifecycle management: An art, not a miracle - The advanced course in Risk Management

FORUM Institut für Management GmbH (147)

- The role of RMP and PSUR in the drug lifecycle - Writing pharmacovigilance documents - QPPV oversight - Impact of EU assessment reports on RMPs and PSURs - Effective global management and harmonisation of RMPs and PSURs - Additional risk minimisati...

• Webinar
• Ohne Einstufung

• 06.11.2024

PREFERRED

Webcast: UPC Fireside Chat - Discuss every four months current legal problems and recent decisions of the Unified Patent Court

FORUM Institut für Management GmbH (147)

- Selection of case-law from the different UPC divisions - Disputed case-law: How to assess diverging decisions - Detailed presentation of the cases and their impact on your legal practice - Written summaries of the relevant decisions - Access to re...

• Webinar
• Ohne Einstufung

• 04.07.2024
• weiterer Termin verfügbar

PREFERRED

CMC dossier requirements for biologics: FDA vs EU - Marketing Authorisation of large molecues in the US with a focus on CMC

FORUM Institut für Management GmbH (147)

- Regulatory landscape in the US - Scientific advice - The IND and BLA procedure - Post-approval/maintenance: Procedures and documentation - Quality data for marketing authorisation - Case studies CMC requirements in the US: After having attended the...

• Webinar
• Ohne Einstufung

• 23.10.2024

PREFERRED

GxP-Regulated Archiving - How to act in compliance with GMP/GLP/GCP

FORUM Institut für Management GmbH (147)

- Compliance requirements within the GMP, GLP, and GCP framework in the pharmaceutical sector - Audit security, electronic archiving, outsourcing - Customized case study workshop: giving priority to your real-life cases - Audits and inspection of arc...

• Webinar
• Ohne Einstufung

• 24.09.2024

PREFERRED

European Patent Drafting Camp - Mechanics, medical technology, electronics, computer-implemented inventions, artificial intelligence

FORUM Institut für Management GmbH (147)

- How to formulate the technical problem and the advantages of the invention - EP claim drafting: tips and tricks; pitfalls to avoid - Drafting specialized and complex claims - Extensive drafting exercises and case studies on the basis of recent EPO...

• Webinar
• Ohne Einstufung

• 16.10.2024 - 17.10.2024

PREFERRED

EPAC 2024: Exam Prep And Mock

FORUM Institut für Management GmbH (147)

- The EPAC exam explained - what EPAC exam candidates need to know - Detailed analysis of selected questions from recent EPAC exams and mock exams - Lessons learned from the last EPAC exams - Our unique EPAC mock exam: new examlike multiple choice an...

• Webinar
• Ohne Einstufung

• 19.09.2024

PREFERRED

Webcast series Development of RNA-based drugs and oligonucleotides - Critical aspects of non-clinical and CMC drug development, analytics, manufacturi

FORUM Institut für Management GmbH (147)

- Concept: Five weekly live webcasts à 2 hours with longtime experienced speakers - Topics covered: Non-clinical aspects, principles and challenges during drug development, regulatory requirements, CQA and analytical tools, formulation - Your benefit...

• Webinar
• Ohne Einstufung

• 11.09.2024 - 11.12.2024, Online (DE)

PREFERRED

CMC Management in Regulatory Affairs - Quality data for marketing authorisation in Europe

FORUM Institut für Management GmbH (147)

- Regulatory requirements in the EU and the ICH region - Essential quality data for marketing authorisation - CMC documentation: Module 3, ASMF, CEP and Quality Overall Summary - Management of post-approval changes - Classification of quality related...

• Webinar
• Ohne Einstufung

• 12.11.2024 - 13.11.2024