ABC provides IND-enabling, registration, and post-commercialization support for the development, quality control, and lifecycle of innovative therapies and generic medicines. Through development know-how, cross-disciplinary technical expertise, and applied experience with evolving global regulatory frameworks, we help efficiently advance and manage programs for large and small molecule drugs, medical devices, and combination products. Better insight. Better outcomes. Ask ABC.ABC Laboratories: Pharmaceutical Development Expertise
Over our more than two decades’ experience with drug chemistries, ABC has worked with virtually every class and type of compound, across most indications and all common delivery systems. We have contributed data to and drafted sections of IND, NDA and ANDA submissions for dozens of commercial products. And we’ve helped hundreds of companies like yours answer challenging development questions, respond to regulators and uncover sources of problematic manufacturing issues.
Click here for more on ABC's Pharmaceutical Capabilities.
No comments:
Post a Comment