Expertise

Forster Legal advises on legal issues in the field of pharmaceutical and medical device law and focuses in particular on research institutions and pharmaceutical companies. The expertise covers all phases of product development - from basic research and approval procedures to marketing and dispute resolution. The transactions are typically cross-border and, if required, are carried out in cooperation with a network of international experts in related consulting fields such as patent law, quality assurance or financing.

 

The law firm's expertise includes in particular:


Basic Research: Confidentiality Agreements, Material Transfer, Feasibility Studies, Contract Research, Cooperation Agreements between industry and universities.

Basic Research

Confidentiality Agreements, Material Transfer, Feasibility Studies, Contract Research, Cooperation Agreements between industry and universities.

Pre-clinical Phase: Research & Development Agreements, Consulting Agreements, expert opinions and demarcation issues under pharmaceutical or medical device law.

Pre-clinical Phase

Research & Development Agreements, Consulting Agreements, expert opinions and demarcation issues under pharmaceutical or medical device law.

Clinical Trials: Clinical Trial Agreements (all phases), CRO Agreements, Service Agreements with HCPs, Data Protection Agreements.

Clinical Trials

Clinical Trial Agreements (all phases), CRO Agreements, Service Agreements with HCPs, Data Protection Agreements.

Market Access & Advertising: Process development, technology transfer, Contract Manufacturing, Cooperation Agreements, Licensing Agreements, medicinal product advertising law.

Market Access & Advertising

Process development, technology transfer, Contract Manufacturing, Cooperation Agreements, Licensing Agreements, medicinal product advertising law.

Purchasing & Sales: Strategic alliances, supply contracts, distribution, warehousing, logistics, antitrust law.

Purchasing & Sales

Strategic alliances, supply contracts, distribution, warehousing, logistics, antitrust law.

Post-authorization: Phase IV trials, Pharmacovigilance Agreements, compliance, Sponsorship Agreements, industry codes, liability and sanctions, dispute resolution.

Post-authorization

Phase IV trials, Pharmacovigilance Agreements, compliance, Sponsorship Agreements, industry codes, liability and sanctions, dispute resolution.