We at Esteve Química offer customized solutions to the pharmaceutical industry: Process development and manufacture of advance intermediate products and active ingredients, from grams to tons, always under GMP standards and environmental protection.
With more than 35 years' experience, we have successfully collaborated with some of the main pharmaceutical companies thanks to effective two-way communication and mutual trust. Our premises have been inspected and approved not only by European, American and Japanese authorities, but also by the most demanding "regulators": our clients.
Our raison d'être is always oriented towards the client and may be summarized as follows:
| • | Identifying the specific needs of each client. |
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| • | Communicating with client along the whole value chain: from R&D through to Commercial. |
| • | Agreeing priorities with client for best possible response. |
| • | Involving client in decision making from the very start to set common objectives and minimize risks. |
| • | Providing client with excellent technical and regulatory support. |
| • | Meeting the needs of client according to product life cycles. |
| • | Communicating openly and transparently, directly and/or through multifunctional equipment. |
Visit R&D and technologies for chemical process development abilities.
| • | Laboratory scale development |
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| • | Pilot plant |
| • | Analytical development / Spectroscopic research |
| • | Semi-industrial plant |
| • | Industrial activity support |
We provide our clients with a global solution: From the first stages of chemical process development through to industrial production, adding pharmaceutical facilities as needed. Also, our production flexibility allows adapting to the requirements of each stage of the product life cycle.
