1. GMP consultation (site layout, documentation system training).
2. Patent check and “free to operate opinion”.
3. Our qualified experts are ready to work as independent party for inspection of API’s.
4. Gap analysis of analytical and technological documents in the context of the development and authorization of medicinal products.

Training Programs specifically designed for pharmaceutical companies to address essential topics:

1. CTD File Preparation.
2. Onsite Analyst Training.
3. Customized In–House Training courses on cGMP.
4. Laboratory accreditation according to ISO 17025.
5. Structural based chromatographic method development / trouble shooting.