Navigating TITCK’s Latest Guidance: Which Products Are Excluded from Medical Device Regulations?
In the rapidly evolving landscape of Turkish healthcare regulations, distinguishing between a “medical device” and a “general use product” is critical for manufacturers and importers. The Turkish Pharmaceutical and Medical Device Agency (TITCK) recently published a vital announcement regarding products that do not fall within the scope of the Medical Device Regulations (MDR) and In […]
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