Health products are products used to protect and improve human health. It is of utmost importance that these products are safe, effective and of good quality. Health product policy and standards therefore cover the regulation of the development, production, distribution and use of these products.
Health product policy consists of a set of principles and practices aimed at ensuring the safety, efficacy and quality of health products at all stages.
These policies include the following elements:
Health Product Standards:
Health product standards are technical requirements that determine the safety, efficacy and quality of health products. These standards are set by national and international organizations.
National Standards:
In Turkiye, national standards for healthcare products are set by the Turkish Standards Institute (TSE). TSE prepares Turkish Standards (TS), taking into account international standards such as ISO.
International Standards:
International standards are set by organizations such as the World Health Organization (WHO), the International Codex of Medicines (Codex Alimentarius) and the International Organization for Standardization (ISO).
The importance of health product policy and standards:
Health product policy and standards are essential for the protection and improvement of human health.
Thanks to these policies and standards:
Note: This information is for general information purposes. It is important to consult the relevant authorities for legal and technical regulations regarding health product policy and standards.
Medical products are of critical importance for human health. Therefore, it is vital that production processes are carried out with the highest standards and rigor. Having a strong production power and vision in the production of medical products directly affects both the safety of patients and the success of the company.
Strong Production Power:
-Appropriate facilities and equipment: The production of medical products requires specialized facilities and equipment. These facilities must be designed and operated in accordance with international standards of good manufacturing practice. Equipment must also be regularly calibrated and maintained. STERVAC Aspiration Systems, with its strong production and research facilities, is the power behind its products at all times and under all conditions.
-Qualified personnel: Personnel working in the production of medicinal products must be trained and experienced in the relevant field. Personnel should also be informed and trained on GMP and other relevant procedures.
-Quality control and assurance: Medical products need to be strictly controlled and tested at every stage. Quality control and assurance systems must ensure that products comply with all quality standards.
Visionary Approach:
Patient-centeredness: Medical product manufacturers must always prioritize the needs and safety of patients. Product development and manufacturing processes should be oriented to best meet the needs of patients.
-Invest in research and development: Medical product manufacturers should invest in research and development (R&D) to develop new and more effective treatments. R&D will contribute to the development of innovative products and improve patients' quality of life.
-Continuous improvement: Medical product manufacturers should strive to continuously improve their production processes and products. New technologies and methods should be pursued and integrated into production processes.
Having a strong manufacturing strength and vision in medical product production provides the following benefits:
Medical products are one of the most important elements of human life. Aware of this responsibility, medical product manufacturers should always strive to produce to the highest standards and meet the needs of patients.