Quality control (QC) processes and documents development / improving and implementation:

- Specifications development (for API and excipients, raw and packing materials, semi and final products, reagents and chemicals),

- Development of IPC (In-process control) program,

- Development and validation of Analytical Methods (AMV) quality control,

- Selection of main and auxiliary quality control equipment,

- Stability Study organization (documents, equipment, processes),

- Staff research and coaching.