Yes, AIT Pharmaceuticals Project conducts regular audits to assess compliance with regulatory standards. These audits are essential to ensure that the manufacturing processes, quality control procedures, and documentation systems adhere to the requirements set forth by regulatory authorities. By conducting audits at scheduled intervals, AIT Pharmaceuticals Project can identify any deviations from regulatory standards and implement corrective actions promptly to maintain compliance. These audits may include internal audits conducted by the company’s quality assurance team, as well as external audits carried out by regulatory agencies or third-party auditors. The goal of these audits is to uphold the highest standards of quality, safety, and regulatory compliance in the production of pharmaceutical products.
