eBook: Successfully navigating complex and evolving regulatory environment for combination products
Posted: 28 August 2024 | West Pharmaceutical Services | No comments yet
With complex processes and stringent regulatory requirements, the path to developing a combination product can be uncertain and challenging
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Every country, region, and territory has its own regulations, guidance, and standards for drugs and devices. Trying to get a handle on that can be overwhelming. Fortunately, with West, you’ll be able to understand and interpret the regulations applicable to your product. West experts are active in industry working groups that provide input into draft guidance and comment on regulations. Located in multiple geographies, they provide diverse geographical regulatory knowledge and insights. They have a unique and in-depth understanding of your products and
associated regional policies. It all leads to mitigating risk and increasing your probability of regulatory success.
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Biologics, Biopharmaceuticals, Clinical Trials, Drug Delivery Systems, Good Manufacturing Practice (GMP), Manufacturing, Medical Devices, Packaging, Regulation & Legislation