Developing a new pharmaceutical drug is a complex and challenging process. EMD Millipore offers you specific expertise and equipment in a number of fields, backed up by a complete matrix of production technologies capable of fulfilling more than 95 percent of all common chemical reactions.
Benefit from our specific expertise in organometallic reactions and asymmetric hydrogenation as well as manufacturing of active pharmaceutical ingredients for parenteral applications.
We provide full service throughout the entire development chain – from early phase up to launch of your product – supporting you in chemical as well as regulatory aspects. You can expect cGMP-certified and regularly FDA-inspected development and production sites, highest standards in analytical services, state-of-the-art equipment covering a broad range of volumes as well as regulatory support (CTD documentation, certificates, DMF).
If you would like further information, please contact us.
We would be delighted to hear from you and we look forward to collaborating with you!