Eviva Pharma was established in 2008, as a pharmaceutical consulting company, to provide chemistry, manufacturing and controls (CMC) consultancy to the pharmaceutical industry.
We have CMC pharmaceutical consulting experience of drug development in pre-clinical products through to marketed products and can help you develop your product every step of the way; from pre-formulation development, selection of a contract development organisation (CDO) and manufacturer (CRM) to developing and validating analytical methods. We also assist in the compilation of your regulatory submission (e.g. CTX/IMPD/IND/Module 3).
We have expertise in the following areas:
We work on a very flexible basis and are happy to assist when you would like one-off CMC pharmaceutical consulting or when you require involvement at each step of the pharmaceutical development of your product.
Please contact us for further information.