FocusFreda's on-site inspection of drug registration production and GMP compliance inspection smoothly carried out
Recently, the Shandong Provincial Evaluation and inspection Center verification team went to FocusFreda to carry out a four-day drug registration production site inspection and GMP compliance inspection. Members of the FocusFreda leadership team attended the meeting and had detailed communication and exchanges with experts of the verification team.
This registration is the first domestic registration of pharmaceutical grade products of FocusFreda. In order to meet the arrival of the verification team, various departments of the enterprise have carried out a lot of preparatory work. After an all-round inspection of the enterprise, the verification team expressed full recognition of the pharmaceutical production quality management and sodium hyaluronate registration work of the enterprise, announced that FocusFreda sodium hyaluronate registration production site inspection passed, and the GMP compliance inspection will be evaluated after rectification, and put forward rectification suggestions for the inspection. The enterprise will quickly rectify the problems found in the inspection, and the subsequent production quality management will be carried out in strict accordance with the verification requirements.
The smooth development of this inspection marks a brand-new step for FocusFreda. In the future, the company will continue to strengthen drug production quality management and drug registration, improve product quality and market competitiveness, and contribute to the healthy development of the pharmaceutical production industry.
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