The development of pharmaceutical medicines is a complex and scientifically-driven process that requires rigorous testing to ensure safety, efficacy, and quality.

The creation of custom reference standards plays a crucial role in analytical chemistry, providing a foundation for accurate and reliable measurements. Reference standards serve as benchmarks against which the quality, identity, and quantity of analytes c...

Reference standards play an important role in quality assurance, as they are essential for calibration, characterization, qualification and validation of instruments and processes.

Quality control in the pharmaceutical industry essentially depends on the speed and accuracy of inspection to ensure drug safety.

Focusing on the production stage, carried out in the industry, we can mention professions aligned with research, development and testing of medicines.