Offering expertise in managing complex multidisciplinary projects. With a wealth of experience and technical prowess, we excel in manufacturing, packaging, clean utilities, and laboratory processes. Our engineers bring operational know-how in Life Science manufacturing to ensure efficient project execution.
Recognizing the critical importance of speed-to-market, we prioritize seamless integration of design, construction, commissioning, and validation, coupled with a smooth regulatory approvals process involving FDA, EU, EPA, and OSHA. From the outset, we prioritize constructability and regulatory compliance best practices, ensuring projects meet stringent standards without compromise.
- cGMP Validation: We provide thorough validation services to ensure compliance with current Good Manufacturing Practices (cGMP), ensuring the quality and safety of pharmaceutical and biotechnology facilities.
- Commissioning: Our expert commissioning services ensure that your facilities and equipment are properly installed, tested, and operational according to industry standards and regulatory requirements.
- Cleanroom Test & Certification: We offer comprehensive testing and certification services for cleanrooms, ensuring optimal performance and adherence to cleanliness standards for sensitive operations.
- HEPA Filtration Challenge Testing: Our rigorous testing procedures assess the effectiveness of HEPA filtration systems, crucial for maintaining clean air quality in controlled environments such as laboratories and manufacturing facilities.
- Lab Fume Hood Testing and Certification: We conduct thorough testing and certification of laboratory fume hoods to ensure proper containment of hazardous substances and compliance with safety regulations.
- Sterile Manufacturing: Production of pharmaceuticals under sterile conditions to prevent contamination.
- Oral Solid Dosage: Formulation of pharmaceuticals into solid forms such as tablets or capsules for oral administration.
- Bulk API Manufacturing: Large-scale production of active pharmaceutical ingredients (APIs) in bulk quantities.
- Cell and Gene Therapy: Advanced therapies involving manipulation of cells or genes to treat diseases.
- GMP Warehousing: Warehousing facilities compliant with Good Manufacturing Practices (GMP) standards for storage of pharmaceutical products.
- Process Utilities: Essential services like water, steam, and air conditioning required for manufacturing processes.
- Biocontainment: Facilities designed to safely handle hazardous biological materials to prevent their release into the environment.
- Vivaria: Facilities for housing and breeding laboratory animals for research purposes.
- Chemistry Laboratories: Laboratories equipped for chemical analysis, synthesis, and research.
- Laboratories for Educational Facilities: Laboratories in academic institutions for teaching and research purposes in various scientific disciplines.