NeoBioMed Services believes in quality of service par excellence and is joining hands with national and international consulting agencies in providing support to solutions meeting the strictest regulatory norms. Our business associates in the United States and other countries have proven and successful track record as a regulatory, healthcare and scientific professional providing consulting services on US Food and Drug Administration (FDA).
Through associates based in USA, Neo BioMed Services provide access to services relating to all US FDA Regulatory Submissions, Professional Development /Training courses available for US Regulatory Affairs.
Neo BioMed Services can identify and help in securing placements for specialized training programmes including IPR, Patenting, Regulatory and Licensing Issues. Depending on suitable number, tailor made training programmes can be organized with the help of international experts in the field. Neo BioMed Services also facilitates regulatory approvals and provides consultancies on intellectual property strategies and regulatory procedures for approval of products