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.
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.
Services
Eviva Pharma consultancy provides chemistry, manufacturing and controls (CMC) consultancy to the pharmaceutical industry. Jim Rennie - Jim has over 30 year's industrial pharmacy/consultancy experience in both large Pharma at Marian Merrell Dow and Procter and Gamble then as a co-founder of Prova a highly respected contract development organisation.
Eviva offer a broad based pharmaceutical consulting service encompassing all aspects and phases of pharmaceutical development, including formulation development of most drug delivery systems. These range from phase 1 pre-formulation activities to clinical trials manufacturing in support of Pharma IMPD's (formerly CTX) through to troubleshooting secondary manufacturing problems and technology transfers and associated CMC regulatory affairs.
Analytical Chemistry methods are key to ensuring the quality and identity of your product. Eviva Pharma have experience of the analytical chemistry work required during each phase of your product's development including:. Eviva Pharma can help design studies to ensure compliance with ICH guidelines and can review data to confirm it is clear, reliable and compliant.
Our experience is mainly for applications with a high Chemistry and Manufacturing Controls (CMC) content such as new chemical entities for Investigational Medicinal Products Dossiers (IMPDs) and Investigational New Drugs (INDs) as well as later stage including predominantly generic and OTC Marketing Authorisation Applications (MAAs).
CMC Consultant - where you do not have the resource or commitment for a full time permanent employee, why not consider an Interim Manager?. No extras such as National Insurance, pensions, healthcare, car, sickness or death in service benefits. Conveniently situated in Camberley, Surrey near to Heathrow and Gatwick airports we can work in the UK Home Counties including Oxford, Cambridge and London.
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