PharmaBioServ was established in February, 1993, as a service company focused on managing Technology Transfer projects for life science manufacturers.  Our original projects expedited new products launch and marketed products optimization and compliance with regulatory agencies requirements.  Currently, we are proud to be the largest regulatory compliance and validation company in Puerto Rico, providing its knowledgeable consultants and expertise around the Globe.  Having a stable leadership team, the lowest turnover rate in the industry, and five star satisfaction, has allowed us to differentiate ourselves through our consistency, compliance expertise and cost value.  Our areas of service include: Project Management, cGMP compliance, Audits, Quality Systems, Remediation, Regulatory Affairs, Qualification and Validation, Contingent Workforce, Personnel Outsourcing, and Training to Pharmaceutical/Biotech, Medical Devices, Food, Cosmetics and related industries.

Our diverse team offers an integrated service structure designed to provide complete solutions for our client needs. We also offer educational programs that provide technical courses within a team setting environment. Our main objective is to enhance the understanding of theoretical and practical elements in these industries by providing the latest key skills from well experienced Senior Level resources. Our hands-on workshops, and certifications programs addressing the latest industry trends and regulations.

Today, with more than 27 years of experience, we continue to provide our clients with world-class direct contract, consulting, placement and testing services, positioning our company as a global source for efficient and compliant operations.

Biotechnology

Medical Devices

Pharmaceutical

PharmaBioServ

The Madrid office focuses on coordinating European operations and streamlining processes across the region.

Madrid

PharmaBioServ's headquarters in Dorado, Puerto Rico

People (1)

Jobs (0)

Other offices