Combination Products Handbook: Regulations and Best Practices

By Susan Neadle

Combination products are therapeutic and diagnostic products that combine drugs, devices, and/ or biological products. According to the US Food and Drug Administration (FDA), “a combination product is one composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device and a biological product.” Examples include prefilled syringes, pen injectors, autoinjectors, inhalers, transdermal delivery systems, drug-eluting stents, and kits containing drug administration devices co-packaged with drugs and/or biological products. This handbook provides the most up-to-date information on the development of combination products, from the technology involved to successful delivery to market. The authors present important and up-to-the-minute pre- and post-market reviews of international combination product regulations, guidance, considerations, and best practices.

This handbook:

• Brings clarity of understanding for global combination products guidance and regulations
• Reviews the current state-of-the-art considerations and best practices spanning the combination product lifecycle, pre-market through post-market
• Reviews medical product classification and assignment issues faced by global regulatory authorities and industry

The editor is a recognized international Combination Products and Medical Device expert with over 35 years of industry experience and has an outstanding team of contributors. Endorsed by AAMI – Association for the Advancement of Medical Instrumentation.

Product Details

• Publisher‏: ‎CRC Press; 1st edition (May 16, 2023)
• Language‏: ‎English
• eBook Digital‏: ‎592 pages
• ISBN-10‏: ‎1032291621
• ISBN-13‏: ‎978-1032291628