Licensing & Registration

Pharmaceutical Licensing, Registration and Compliance: Verifiable Credentials with Relevant Domestic and International Authorities

Sentry BioPharma Services ApS (Sentry ApS) demonstrates a collaborative approach to pharmaceutical licensing and regulation. The regulations and directives of the Danish Medicines Agency (DMA), European Medicines Agency (EMA), World Health organization (WHO), and the U.S. Food and Drug Administration (FDA), function as the foundation for Sentry ApS’ GMP storage and pharmaceutical distribution services. By effectively communicating with regulatory authorities at national and global levels, Sentry ApS develops timely, highly efficient, and compliant solutions to fulfill client needs. Frequent customer audits and inspections provide valuable direction and feedback, enabling Sentry ApS to maintain an exemplary compliance history. Years of industry experience, continuing education, and industry involvement prepare the Sentry ApS leadership team to rapidly acclimate to shifting pharmaceutical regulations. Assured compliance empowers clients to focus on research, efficiency and other differentiators.