Teva Pharmachemie is a strategic player in the field of development and production of oncology injectables and dry powder inhalation products. With our state of the art manufacturing site we have reached high working standards leading to cGMP approval of all major Health Authorities of the world (i.e. EU, USA, Japan). At Teva Pharmachemie we offer an effective combination of services in a modular way.
- Teva Pharmachemie can be your partner for the manufacturing of development and commercial scale production.
- We have a specific knowledge in drug product development and drug manufacturing from early phase (phase 2 or 3) to commercialization.
- To make a smooth technology transfer possible and to guarantee that development and production have a good fit, a multidisciplinary dedicated team shall support the development of your product in specialized laboratory and manufacturing environments.
If you have a product in development and are looking for a transfer to a commercial size GMP manufacturing environment, we can be your partner.
- Teva Pharmachemie provides a wide range of Regulatory Services in all phases of your product life cycle; from early-stage development to market authorisation and post approval stages.
- Teva Pharmachemie has established a sales, marketing, and distribution organization with global capabilities.
With our Marketing & Sales organisation, we can combine our marketing presence with our customer’s portfolio and explore opportunities for commercial collaboration.
Being part of Teva, we have access to the worldwide marketing & sales network of the Teva Group in addition to our own sales organizations in The Netherlands.