Neo BioMed Services has been engaged, since 2006, in providing expert technical, regulatory compliance and business support services to Small and Mid-Size Pharmaceutical, Biotechnology, Stem Cell, Biologics, Diagnostic, Medical Devices and allied Health Industries including biodefense industries.
Neo BioMed 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 associates are proficient in development, implementation and management of diversified manufacturing and supply chain projects involving the integration of scientific principles, regulatory aspects and business requirements and management.
Neo BioMed Services assist the stakeholders to develop cGMP compliant quality products from concept to commercialization, effective Technology Transfer, regulatory submissions, liaisoning and necessary government approvals. Services are focused on cGMP regulated clinical or commercial Active Pharmaceutical Ingredients (APIs), Rx and OTC drug products, Diagnostic products and tools or Medical Devices.
NeoBioMed Services founded in May 2006 is a Partnership Firm incorporated in India under the Indian Companies Act, 1956, and now governed under the Companies Act 2013 and having its registered office in New Delhi, India. The company is led by a management team headed by its Chief Executive Officer Dr. Brij M. Gandhi, a scientist and a technocrat with more than 47 years of experience as scientist, science manager and policy administrator with the Government of India, and consultant and service provider.
The Company has been engaged, since 2006, in providing expert technical, regulatory compliance, business support and technical services to Small and Mid-Size industries including Pharmaceutical, Biotechnology, Stem Cell & Regenerative Medicine, Biologics, Diagnostic, Medical Devices, Allied Health Industries and biodefense industries.
The company helps in obtaining Government regulatory approvals and providing complete solutions for import and export of bulk drugs, APIs, other intermediaries and chemicals including the regulatory issues involving government dealings, registration of the products and marketing authorizations, technology transfer, entry India issues etc. It helps in securing registration of manufacturing plant of Bulk drugs, products and formulations for ultimate Import of the drugs into the country; Grant of test license for drugs, approvals of Protocols for BE / CT and issues of final permissions for Manufacturing & Marketing of Bulk drugs & Formulations, Issue of Import license, Export permission for drugs.View More