pharmavize

With over 20 years experience, Pharmavize is an experienced provider of Chemistry, Manufacturing and Control (CMC) services to the pharmaceutical and biotechnology Industry. We help accelerate our clients drug development and approval process by offering high quality services in CMC Dossier development, Contract Development and Contract Manufacturing. We have expertise in human and veterinary drug development and experience to partner with start-ups as well as worlds leading pharmaceutical companies. CMC DOSSIER DEVELOPMENT SERVICES: A consistent and compliant regulatory dossier is mandatory to obtain clinical trial approval or smooth marketing authorization (MA). Our experienced Dossier Development Team can help to accelerate your drug approval process. We are experts in writing and formatting supporting documentation, whether it is a scientific report, a quality document or a regulatory dossier. Our broad portfolio of writing and formatting services ranges from data review & reporting to regulatory dossier writing and submission. CONTRACT DEVELOPMENT SERVICES: Every phase in the development of a drug is crucial and requires specific knowhow. Pharmavize uses dedicated teams to identify the right approach for your research project. Our research services are focused on developing cost-effective methods and technologies. We can provide you with formulation & process development services, analytical development services and stability studies. CONTRACT MANUFACTURING SERVICES: The production of investigational products is not a routine job. In the early development phase, it is unlikely to have a well-defined manufacturing process or lab analytics in place. We have the knowhow to manufacture and label early-phase clinical trial material according to GMP appropriate standards. We can manufacture various dosage forms. We are experts in small-scale manufacturing: no batch is too small!