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TechFlex is the catalyst for success in the medical device industry, offering comprehensive support to growing companies. With expertise spanning from initial concept to market entry, TechFlex provides tailored solutions, cutting-edge technologies, and regulatory guidance.
Regarding the ongoing lawsuit challenging FDA regulation of laboratory-developed tests (LDTs) as medical devices, the US District Court, Eastern District of Texas ruled the FDA does not have the legal authority to regulate lab-developed tests.
Read the full article at: telcor.com
