Synapse Pharma Consulting

We Synapse Pharma Consulting collaborate with academia, pharmaceutical manufacturers and regulatory agencies fostering a synergistic relationship, transmitting knowledge and enhancing global health. We are one-stop solution provider covering regulatory, market access strategy and GMP compliance. We offer academic programs into the pharmaceutical industry entails providing comprehensive insights of the evolving regulatory landscape, practical insights into Quality Management Systems and GMP compliance. To collaborate with our academic program, please connect to info.synapse.pc@gmail.com. We are go-to consulting partner for micro, small and medium size pharmaceutical manufacturers in navigating complex regulatory requirements and obtaining regulatory approvals i.e. GMP accreditation, USDMF (API, Intermediates, Packaging Materials, Excipients, Type V MF), CEP, ASMF, EDMF, WHO-MF, and Marketing Authorization Application (NDA, ANDA, EU-Dossier) across the globe (US, EU, Japan, Brazil, Canada, Latin America, China, Korea, African countries, ZAZIBONA, EEA countries, Asia & Russia) by conducting regulatory gap analyses, preparing regulatory submissions, managing interactions with regulatory agencies and conducting Good Manufacturing Practice (GMP) compliance audits. To collaborate with our subject matter experts please connect to bd.synapse.pc@gmail.com. We conduct research, participate in review of changes in regulatory guidelines, policies and standards within the pharma industry. With our entrenched contacts, we support pharma aspirants in exploring diverse career pathways within the pharmaceutical sector, including research and development, regulatory affairs, clinical operations, marketing, sales, consulting, and entrepreneurship. Please register with us on hr.synapse.pc@gmail.com