This live webcast provides you regularly with the detailed presentation of the EPO's Boards of Appeal on computer-implemented inventions and their impact on your prosecution practice.
Our speaker, one of the leading SPC experts in Europe, will discuss the SPC referrals to the ECJ with you. He will put the decisions in context and will show you the consequences for national court practice and for your application practice.
Learn how to write digital patent applications which get granted and are infringed upon! This online course will give you the best practical tips to improve your skills in drafting claims for digital patents. Apply your knowledge in a practical test including feedback from our speaker, an experienced litigation expert.
This Forum!Live online course aims at providing a toolbox for improving procedures and outcomes of the IP department. This should facilitate making the IP department even a more costsensitive profit center.
This online training will give you in-depth knowledge on the CMC requirements for marketing authorisation. Take the chance to participate in our virtual seminar via Zoom.
This online course provides guidance on uncommon parts of the procedures, explaining the major steps to be taken and the best practices to avoid further complications. In addition, the major differences and difficulties in states outside Europe are covered to provide a more global view.
This online course is about IP audits. Attendees will learn how to set up a proper IP audit plan and write a fitting IP audit report.
In this FORUM!Live online course our experienced speakers will help you to be prepared for FTO challenges when your company or your client wants to introduce new products or enhance existing ones. They will discuss with you best practices for setting up time and cost sensitive FTO searches and drafting effective FTO opinions.
Your pre-meeting: Be prepared for your event
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 and pharmacovigilance at your fingertips!
Our speakers will show you strategies for a Patent Due Diligence. You will learn how a Patent Due Diligence can be conducted efficiently. You will be able to test your Patent Due Diligence skills by the means of practical exercises under the guidance of the speakers.
English language in intellectual property as an intercultural communication tool can be a barrier to filter distort communication.
This practical online course deals with the impact of the Fourth Industrial Revolution on intellectual property practice. Attendees will be provided with valuable knowledge as well as practical methods and tools using digital patents in digital business models.
This training addresses the new regulatory framework for drug-device combination products. Use this opportunity to discuss the impact these changes will have on your products and how to implement the requirements. The training course will be entirely held in english.
To make the most of ICH Q12 opportunities you as a lifecycle manager have to be aware of the relation between ICH guidelines Q8 to Q12 and how to properly integrate them. Our experts will go through each guideline and train you on the desired outcome of mastering QbD.
This online practical course is a practitioner's guide on how and where to win global patent litigation cases. One lead speaker and author of a standard reference and three speakers from different industries cover all relevant angles of global patent litigation.
This course is intended for paralegals and IP administrators and will help participants adequately prepare an application for filing with EUIPO/WIPO and provide guidance on administrative aspects such as the required filing documentation, procedural steps, monitoring time limits and fees.
Marketing authorisation and market access in Saudi Arabia, the UAE, Jordan, Iran, Iraq and Turkey. If this is your business goal, don't miss out on this unique course! First-hand information provided by experienced speakers guarantees success.
This online course provides drafting and negotiating advice for EU practitioners, with precise references to existing US law.
Data integrity and audit trail review in the pharmaceutical production: The aim of this online training course is to provide you with tools and tips that will enable you to understand applying requirements to existing systems, to integrate new processes and that will enable you to optimize preparation for inspections. The training course will be entirely held in english.
This live webcast course deals with invention disclosure written by an inventor's knowledge and includes a detailed description of an invention. It is a confidential document. Working closely with inventors, you need to know how to handle an invention disclosure carefully. Become familiar with the requirements of an invention disclosure.
This live webcast course deals with detailed guidance to the formal requirements of the PCT and information on the regulations related to the PCT.
This live webcast course deals with how to protect your patent properly in the USA. This FORUM!Live online course will provide a detailed guidance to the formal requirements of US patent prosecution.
This live webcast provides you regularly with the detailed presentation of the EPO's Boards of Appeal on computer-implemented inventions and their impact on your prosecution practice.
IP Strategy! - the interactive online course which helps you setting up convincing IP strategy plans.
In this FORUM!Live course the strategic IP goals that can be facilitated by patent prosecution strategies will be explored.
The purpose of this live online course is to inform the participants how to prepare an international application for filing under the PCT and subsequently monitor the consecutive procedural steps, timelimits and payment of fees in the PCT international phase up to and including entry into the national phase in designated and elected states.
Our speaker will give you tips and tricks on EP claim drafting and will show you which pitfalls to avoid.
This online course shall provide a sound overview about different local laws in important countries in EU and beyond with respect to employee invention rights. It shall enable the participants to address complex situations when designing and negotiating agreements for cross-border R&D.
The online course will show you how to write scientific and clinical documents such as a technical documentation or clinical evaluation in good and readable English that is appropriate to your audience, while complying with the regulatory requirements.
In our online course our speakers will give you tips and tricks on EP claim drafting and will show you which pitfalls to avoid. Learn more about the deal of European Patent claim drafting and improve your claim drafting skills.
This live webcast course will give you a good introduction to intellectual property rights.
This online seminar provides you with the 'soft skills' for the successful negotiation of patent license agreements. Our speakers will show you the dos and don'ts of patent license negotiations. They will show you how best to prepare for negotiations and what tactics you should follow during negotiations.
PharmaFORUM Webcast Clinical Trials
Our biotech experts will provide you with the latest information on issues related to development, quality and regulatory affairs of biologics every month in a two-hour webcast, in particular with regard to CMC.
This live webcast course will give you a good introduction to intellectual property rights.
The value of patents depends on factors such as competitive advantages, potential for exploitation and legal cover. It plays an important role in, among others, patent purchases, strategic IP portfolio management and mergers & acquisitions. Learn more about the valuation of patents in this online course.
The digital edition of this conference offers you once again the most recent developments in IP for the seed industry and the breeders.
All the essentials of clinical trials in Europe in only two days! Six experts will share their in-depth knowledge with you to introduce you as beginner or update you as professional on the most important aspects. Pose your individual questions in advance or live to make the most of your training!
Our speakers will suggest authoritative answers to key problems of EU design law and give an update on most recent case-law.
This online course helps attendees bridging the innovation gap and improving their IP creation and harvesting process.
Would you like to successfully resist on Chinese market for medical devices? Then attend our webcasts and learn more about the new Chinese regulation for medical devices, how to perfect your pre-market registration and post-market surveillance: Our local experts will provide you with brandnew information!
The most important published and unpublished decisions of the EPO Boards of Appeal 2016-2018 in the field of biotechnology will be presented. The panelists will discuss, in particular, the consequences of these decisions on patent practice.
The course provides practical, hands-on experience in eCTD specifications, eSubmission requirements and data integrity for IDMP, SPOR and XEVMPD. Save your place in our virtual zoom seminar room.
Given the significant global importance of China, European IP practitioners need to have a keen sense of strategic and legal opportunities and threats when doing business with China.
This online training programme consisting of three recorded webcasts will train you how to develop documents, compile them and submit an eCTD step by step.
This e-Learning programme will provide you with detailed knowledge on the classification, grouping and submission of variations in the EU.
Do you need know how regarding CTD/eCTD & CMC? Then this e-learning programme is the fast track to becoming knowledgeable in this field. No prior dossier experience is required.
This e-learning will familiarise you with the regulatory affairs principles outside the ICH region and show you how to categorise the various regions in terms of regulatory requirements. Dossier requirements in Australia, Hong Kong, India, South Korea, Taiwan, Saudi Arabia, GCC, Jordan, Turkey, Thailand, China, South Africa, Russia, Kazakhstan, Eqypt, Brazil, Mexico & Argentina will be addressed
This e-learning programme will familiarise you with the regulatory affairs principles involved in applying for a marketing authorisation in Europe (MRP, DCP, CP) . It will also introduce you to post-authorisation duties (renewal, variation...).
This e-learning will familiarise you with patent portfolio management.
Do you want to gain access to 500 Million people and 24 Million companies in the EU-Single Market as your clients? Serving customers in the EUROPEAN UNION requires GDPR Compliance. If you run a website targeted towards European customers and deal with personal data of your customers, you typically have to follow the rules of the GDPR. If you don't, millions of dollars of fines can be the result.
Digital transformation is solving problems with the best possible technical means. In order to find the right solutions, a fundamental understanding of digital transformation is essential. Use the food for thought and practical examples in this e-learning to identify the improvement potential in your company.
Do you need detailed know how about management accounting function and tasks? This top e-Learning explains the process of preparing management reports and accounts that provide accurate and timely financial and statistical information required by managers to make day-to-day and short-term decisions.
One of the key elements in running any business that uses IT services is the management of IT costs. The company's IT should be used as sustainably as possible and the added value should be demonstrable.
In Germany alone, IT failures and malfunctions cause damage running into billions every year, with the number of attack vectors rising and the threat posed by cyber criminals continuing to grow.
High-quality e-learning for a well-founded understanding of the concept of the Concept of the German Accounting Standards
This e-Learning programme will focus on stability testing for chemical and biological products in the ICH region.
This e-Learning programme will familiarise you with the data requirements in CTD Module 3.
The newly produced e-learning programme helps foreign in-house counsels and human resources managers at international companies to understand the complex legal regulations concerning labour and employment law in Germany. You get an overview of all key aspects of German Employment Law and get an update on court decisions such as unfair dismissal, remuneration and bonus payments, minimum salary etc.
Do you need to be well versed in European pharmacovigilance for your daily work? Then we recommend this e-Learning. You can choose between three different packages according to your level of expertise and requirements.
This live webcast provides you regularly with the detailed presentation of the EPO's Boards of Appeal on computer-implemented inventions and their impact on your prosecution practice.
Evidence generation, value proposition and the HTA - the latest insights with regard to Orphan Drugs
This FORUM!Live online course is about techniques and tools for IP risk mitigation. Attendees will learn how to set up a proper IP risk management process.
During this Summer School you will build a solid toxicological know-how basis and will be informed about the inclusion of toxicological data in the marketing authorisation dossier. Take the chance and participate in our interactive online training.
Online seminar: Gain important knowledge about the task of EU-QPPV
Meet the expert Dr. Ulrich Granzer and get first-hand information, hints and tips for your daily business challenges with FDA approval of a medicine for the US market!
This workshop helps you collect, clean and structure all necessary data for IDMP and informs you on ePI (structured electronic product information) - a digitalisation project potentially utilizing IDMP and SPOR
This online-seminar will provide tips on how to prepare and maintain a core PSMF as well as annexes with the relevant local peculiarities worldwide.
Our experts will help you to identify risks in your PV system and will provide you with helpful methods to adjust your audit processes and strategies. Save your place in our virtual seminar room.
Our online course will provide insights into the current (remote) pharmacovigilance inspection strategy in Europe. Learn all you need to know about the differences in the inspections and about the different requirements in this training. Save your place in our virtual seminar room.
Online Seminar about Generic Market Access & Pricing in Europe
Compassionate Use Programme (CUP) and Named Patient Programme (NPP) - the expertise required to plan and conduct expanded access programmes.
This live webcast provides you regularly with the detailed presentation of the EPO's Boards of Appeal on computer-implemented inventions and their impact on your prosecution practice.
Three experts will give you an in-depth update on your duties with regard to accepted clinical trial data, dossier submission and the post-approval processes in CHINA. Including the latest eCTD specifications of TAIWAN.
How to prepare effectively for the responsibilities of a person responsible for regulatory compliance (PRRC). This and more in our online-seminar via Zoom!
Tips & tricks for managing periodic reports and risk management plans post marketing authorisation. Furthermore insights into global PV document management will be given. Thus the training course gives you an allround overview.
Effective oversight of outsourced activities in the healthcare sector - Prepare yourself for the balancing act between compliance and outsourcing, and learn how to implement your own effective regulatory vendor oversight programme. Save your place today.
This live webcast provides you regularly with the detailed presentation of the EPO's Boards of Appeal on computer-implemented inventions and their impact on your prosecution practice.
This two-day course provides an introduction to medical writing for pharmacovigilance, as well as insights into several relevant safety documents.
The diversity of PV-relevant regulations defining the art of good PV practice call for a finely tuned balance to ensure that all PV systems employed by a company tie into a unified and truly global PV matrix. Our experts in this course will give you a detailed update on the current legal and regulatory background and on your duties.
This live webcast provides you regularly with the detailed presentation of the EPO's Boards of Appeal on computer-implemented inventions and their impact on your prosecution practice.
This live webcast provides you regularly with the detailed presentation of the EPO's Boards of Appeal on computer-implemented inventions and their impact on your prosecution practice.
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 and pharmacovigilance at your fingertips!
This live webcast provides you regularly with the detailed presentation of the EPO's Boards of Appeal on computer-implemented inventions and their impact on your prosecution practice.
Our biotech experts will provide you with the latest information on issues related to development, quality and regulatory affairs of biologics every month in a two-hour webcast, in particular with regard to CMC.
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