Pharmaceutical stability studies are complex and present many challenges. They play an essential role across the lifecycle of pharmaceutical products and in particular, during the development of IND and NDA submissions. Whether you intend to implement your stability programs in-house or by outsourcing, it is important to ensure the integrity and efficiency of your stability studies.
Register now for our webinar series, covering important considerations for efficient stability programs, including the practicalities of working with a contract laboratory, optimising stability protocol design, testing and how to tackle specific product categories such as biopharmaceuticals or inhalation products.
Questions? pharma.services@intertek.com |
