More Than 20 Years of Experience Designing Pharmaceutical and Biotechnology Facilities

P2S engineers bring extensive consulting engineering experience in FDA regulatory compliance. With design and validation of cGLP R&D laboratories and cGMP product and raw material warehouses, manufacturing production, final fill and finish and clinical manufacturing cleanrooms, P2S also provides mechanical and electrical infrastructure (MEP engineering) support for pharmaceutical and biotech facilities. Incorporating enhanced features of highly energy efficient strategies, we take a great pride in our system design approaches to ensure that facilities and buildings are fully compliant to both FDA regulatory and client-specific operational requirements.

P2S is passionate about partnering with its clients, associated design team and review regulatory agencies. This is how we ensure the successful integration of facilities, buildings, systems, infrastructure and project execution. We approach pharmaceutical and biotech projects with teamwork in mind. The P2S GMP specialist team works with FDA and regulatory agencies, client project management and technical teams, architects and other design consultants.

P2S engineers focus on designing high-performance building systems for pharmaceutical and biotech projects that are upgradeable, maintainable and cost-effective to reconfigure and retrofit. Our construction documents are clear and concise and focus on specifying systems, details and facilities designed for maximum life.

P2S understands the importance of keeping facilities operational and regulatory compliant. With a detailed and thorough construction plan and sequencing strategy, the number and duration of utility outages required in modifying existing systems can be minimized. Temporary or alternate utility sources can be specified for critical loads to minimize the ongoing affect the project has on facility operations.