Good Manufacturing Practices (GMP) is a mandatory that must be carried out by the manufacturing industry as regulated by the Indonesian Food and Drug Supervisory Agency (BPOM). One of the requirements is an audit of raw material suppliers. This activity aims to ensure that raw material suppliers have standards according to GMP guidelines.
On July 13, 2021, 2 auditors from PT Errita Pharma conducted an audit of Medion Plastic. The audit was carried out virtually through the zoom application, considering the ongoing Covid-19 pandemic. The audit agenda begins with introductions, presentation of Medion Plastic’s company profile, then continues with the presentation of the production process and discussion, then closes with the presentation of results and conclusions.
The audit implementation went smoothly and well. All inputs are accepted as study material for improvement and improvement of product and service quality. As a result, Medion Plastic was declared “PASS” as a supplier of plastic packaging materials for PT Errita Pharma. “Hopefully Medion and PT Errita can continue to work together in a good and harmonious way,” said the representative of the auditor of PT Errita Pharma.