- Carry out the pharmaceutical development of new formulations and Bimeda's formulas; prepare development and stability test reports, do bibliographic research.
- Develop, review and update product documentation for the transfer of production technology.
- Control the entry and exit of the climatic chambers and send the samples to Quality Control.
- Monitor the stability studies carried out by the company or third parties and carry out critical analysis of the results.
- Make protocols and reports of stability tests of products and stability reports of monitoring of registered products.
- Carry out the preparation of Standard Operating Procedures and keep them in force in the area of Development.
- Monitor the progress of clinical trials.