Regulatory & IND Support

We don’t just deliver your clinical supplies.
We deliver the data, too.

We can help you be prepared for your submission.

The regulatory process is complex, even if you have been through it a few times. The Serán executive and management teams have decades of experience with hundreds of compounds covering nearly every therapeutic area. We know what it takes to pull together the CMC data package for inclusion into your regulatory submission.

Our Project Management and Development team members will work with your regulatory team to establish product and quality objectives. Our scientists and engineers will collect the right amount of data throughout the project lifecycle to ensure reviewers can see that those objectives have been met, and you can get your clinical studies started.



Your committed CMC partner.

Your drug is your future, but the path to a successful product is daunting. You need a CMC partner that’s as committed to your success as you are. Seràn offers a comprehensive set of drug-development services that begins with a detailed understanding of your project and goals. We deploy a science-based methodology that rapidly identifies a preferred approach that will enable an efficient  advancement of your drug to the clinic and beyond. Our science, quality systems, regulatory expertise, and customer service are second to none. 

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Let’s develop together.

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