InsideReg is a Regulatory Affairs Consultancy founded by ex-MHRA Assessor Dr Laura Millichamp. We support companies at all stages of development with regulatory strategy and activities such as submission of Clinical Trial Applications, Orphan Drug Designation, PRIME, Scientific Advice and Marketing Authorisation. We hold Orphan and SME designations through our Irish office and local affiliate services for Clinical Trial and Lifecycle maintenance activities in Switzerland. Our expert teams formulate Clinical, CMC and Non-Clinical development strategies across all therapeutic areas for both small molecule and biological assets in EU, US and Switzerland

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