Venipharm, Your Partner of Choice
Business Development & Licensing
Strategic Alliances Driving Shared Growth
At Venipharm, we believe that innovation and access to healthcare are built on strong, trusted collaborations. We are always open to new partnership opportunities to expand our product portfolio, integrate innovative technologies, and address unmet medical needs for both patients and healthcare professionals. We aim to be the "trusted partner" in all aspects of our business relationships. We want to be more than just a service provider. We actively seek growth through various partnership models: • Licensing-in: Expanding our portfolio of strategic products. • Licensing-out: Offering our partners market-ready products. • Distribution agreements: Maximizing the global reach of our products. • Co-development: Collaborating on the development of innovative solutions.
Why Partner with Us?
We provide our expertise and infrastructure to build successful and long-term partnerships: • A strong network: Presence in over 40 countries with established strategic partners. • A global approach: From R&D to commercialization, with strong regulatory expertise. • Operational excellence: Ensuring optimized product launches and seamless supply continuity. • Contractual flexibility: Tailored solutions and swift decision-making to meet our partners’ specific needs.
Our Licensed Products
We offer a diverse portfolio of products available for licensing and distribution agreements. We believe the greatest innovations arise from strategic collaborations.
Let’s discuss your project!Service & Support
How We Can Support You?
At Venipharm, we understand the critical importance of regulatory compliance and quality in pharmaceutical development. As your partner, we work with you throughout the value chain to ensure that your products meet the most stringent standards and local requirements, while speeding them to market.
Monitoring of Development Projects of Pharmaceutical Forms
Our strengths and areas of expertise: • Quality project management: quality management system, change control, complaints management, supplier quality management, quality compliance management, assistance with annual product quality review (APQR) • Product launch activities • Product technical support • Training • Batch certification • Pharmacovigilance monitoring and medical information
Regulatory Support
Our strengths and areas of expertise: • Preparation of the marketing authorisation submission dossier: coordination, drafting of documents for modules 1, 2.3, 3, national and European procedures and responses to questions from the healthcare authorities. • Drafting and submission of variation applications • Preparation and submission of price request dossiers • Compliance and audit of pharmaceutical documentation • Preparation and submission of MA renewals (France and Europe)