Eviva Pharma

Eviva offer a broad based consultancy experience of both early phase formulations and marketed products. This can involve supervising and selecting the formulation CRO and the GMP manufacturer. Dosage forms include: injections (aqueous, lyophilised, co-solvents, micellar systems); oral dose including hard and soft gelatine capsules and tablets, semi-solids; syrups and suspensions; respiratory products including nebuliser solutions; topicals including gels, creams and ointments. Products include human Rx and OTC products, veterinary products and ‘nutraceuticals’. Eviva Pharma's services include the following:

Pre-formulation; help in designing pre-formulation studies to support the formulationAssignment of potency, standardisation of reference pH-solubility, pH-stabilityBinary mix compatibility/excipient selectionSolvent solubility

FormulationPre-clinical dosage form design Selection of most suitable dosage form to suit the clinical indicationOptimisation of excipients for stability, processability, biological actionShort-term stability studies on candidate formulationStability studies on GMP batch(es)

GMP Manufacture of Drug ProductSelection of appropriate GMP manufacturerOversee confidentiality, commercial and technical agreementsTechnology transferSet finished product specificationsOversee/supervise first batch(es)