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Partnering with Altasciences for your IND/CTA needs will ensure that your application to regulatory agencies moves forward as smoothly and efficiently as possible. To reach your milestones on time, we recommend setting up a meeting to consult with us at least six months before your required submission date.
Contact our experts today.
Altasciences can help you compile the key information necessary to approve your application request, including:
- Animal pharmacology and toxicology studies to assess safety
- Manufacturing processes to ensure consistent batches of the study drug
- Clinical protocols and investigator information to assess tolerance and risk
For a more detailed discussion of the regulatory planning process, consult our Preclinical Assessment Planning Guide.
Altasciences’ Proactive Drug Development platform transforms the traditional outsourcing paradigm by providing you with expertly designed, customized roadmaps that seamlessly bring you from lead candidate selection to clinical proof of concept, and beyond.
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