The evolving EU MDR and IVDR present key opportunities for companies to enhance compliance strategies, engage with notified bodies, and optimize market access. Staying informed and proactively ...

The burgeoning field of Software as a Medical Device (SaMD) offers opportunities for innovation in healthcare monitoring and delivery through mobile apps. Regulatory focus by the FDA on "device ...

Here are three important regulatory changes affecting parenteral packaging that pharmaceutical companies need to be aware of ...

Under the Microscope: Science, Operations, and Regulation in Dermatology Trials ...

MES software is transforming medical plastics manufacturing by automating compliance and enabling real-time traceability.

Innovations in Sterilization & Quality Assurance Propel Reprocessed Medical Devices Market ForwardThe Reprocessed Medical ...

The "FDA Regulatory Compliance for Drug and Biotech Products (Nov 12th - Nov 13th, 2025)" training has been added to ResearchAndMarkets.com's offering. Regulatory Compliance is the level of activity ...

On Dec. 1 in Davis, UC Cooperative Extension is offering in-person training for people to receive certification to measure ...

Opportunities lie in system redesign, enhancing documentation, and training to prevent human error in GMP-regulated environments. Focus on clear SOPs, tailored training, and supportive environments to ...

Shashank Murali is a Quality Assurance professional based in Minneapolis, Minnesota, with more than eight years of experience in the medical device technology area.

Chinese social networking company Weibo's AI division recently released its open source VibeThinker-1.5B —a 1.5 billion ...