compliance with the relevant medicine Regulatory Authorities (Country Specific where applicable), Medicines applications for submission to the regulatory authorities Work in collaboration with internal and external maintain effective relationships with Regulatory Authorities, internal and external stakeholders Formulate
and seminars and by regular self-study of the national/international literature. Provide expert medical/scientific due regard to all applicable local, global and national laws, regulations, guidelines, codes of conduct registry/database projects, epidemiological surveys, post-authorization studies (phase IV), IIS projects, etc.): all
Assurance / Quality Control function. Preferable: National Diploma or B Tech. in Plastics / Polymer Technology