Our team of qualified personnel is ready to assist you to address all your production and pharmaceutical challenges in:
- Process development and manufacture of APIs according to cGMP standards
- Production of laboratory batches and scale up small productions
- Validation of laboratory batches. It includes process and purification validation.
- The expertise and capability to establish the Drug Master File for your API
We can provide for you:
- production of API intermediates under cGMP conditions or non GMP conditions.
- production of advanced intermediates with complete cGMP analytical services and registration documentation.
- process development or technology transfer and CMO manufacturing.
Our experience gives us the confidence to tackle and address each one of your challenges with the purity of the products.
We can produce substances containing elements up to the ppb level. Our facilities can handle any separation and purification processes:
We provide quality control services according to the regulatory requirements of the country of your business operations. Our dedicated and experienced specialists are ready to support your pharmaceutical and chemical development and production activities.Read more
In the pharmaceutical and chemical industries, research and development are extremely important in the process of product development and successful production. Our team of dedicated and experienced experts are ready to share their know-how to support your activities in:
- Development of optimal synthetic way for manufacturing of APIs, API intermediates and specialized chemicals
- Process optimization, scale up (production) and validation according to cGMP standards.
- Development and validation of analytical methods