Regulatory requirements for product registration can be overwhelming. They’re complex, vary by country, and frequently change. We know they’re important (safe medicines, yes!), but what does it actually take to get a product from the manufacturing plant onto the shelves in your local pharmacy? Let’s take a look together.
The USAID-funded Expanding Effective Contraceptive Options (EECO) project, led by Catalyst Global, developed the Product Registration Toolkit. It helps guide regulatory experts and non-experts alike through the process of registering health products, like contraceptives, in low- and middle-income countries (LMICs). The digital collection of adaptable resources includes:
Each will help you navigate the process of product registration from start to finish.
Check out the two-minute overview of the toolkit below.
Preparing for product registration is a daunting task, but we’re here to help. The Product Registration Toolkit is a tour of the inner workings of the process. You’ll get a glimpse of each step along the way and leave with adaptable tools to support your own registration in an LMIC.
Take a peek at what you’ll find inside the Product Registration Toolkit:
You can find the full toolkit, with downloadable copies of the resources, here.
For any questions or inquiries regarding EECO’s Product Registration Toolkit, please reach out to Shannon Bledsoe.