Business Details
42 Years
experience
Your Trusted Partner for GMP Design Solutions
Established in 1984, Ce & Ic is a full-service engineering and architectural design firm dedicated to serving the pharmaceutical, biotechnology, and specialty chemical industries. Our expertise spans 35+ years of delivering projects that adhere to US FDA, EU, and global regulatory standards, emphasizing efficiency, compliance, and robust design solutions. We pride ourselves on proactive problem-solving, fostering innovation, and maintaining long-term client relationships that often exceed two decades. Our comprehensive services include planning, conceptual and detailed design, consulting, and construction support, ensuring clients receive end-to-end project delivery. With a team of seasoned professionals, we integrate process, mechanical, electrical, and civil engineering with architecture to create facilities that meet functional and regulatory demands.Our commitment to quality is reflected in hundreds of successful projects, ranging from biologics manufacturing to potent compound containment. We prioritize cost-effective solutions without compromising compliance, leveraging 2D/3D CAD technologies and deep domain expertise. Our clients benefit from tailored services such as capacity studies, risk assessments, and technology evaluations. Ce & Ics reputation is built on a workforce with over 17 years of average tenure, ensuring continuity and institutional knowledge. We are recognized for designing facilities that balance flexibility with operational excellence, including cleanrooms, QC labs, and bio-safety systems. Our mission remains unchanged: to add value from project inception to commissioning through coordinated, detail-oriented design.
Services
GMP Design
Biologics Manufacturing
API Production
Sterile Fill-Finish
Potent Compound Containment
Consulting Services
Construction Assistance
Laboratory Design
Facility Planning
Regulatory Compliance
Details
- Year established: 1984
Highlights and features
- We have over 35 years of experience in GMP engineering design.
- Our team provides efficient and cost-effective solutions.
- We offer end-to-end project support from planning to commissioning.
- Our designs ensure US FDA and EU regulatory compliance.
- We maintain long-term client relationships spanning over 20 years.
Services
GMP Design
Ce & Ic specializes in GMP design for pharmaceutical and biotechnological facilities, ensuring adherence to US FDA, EU, and international standards. Our solutions integrate efficient process flows, regulatory compliance, and robust infrastructure. Clients benefit from tailored designs that balance operational flexibility with cost-effectiveness.
Biologics Manufacturing
We deliver end-to-end biologics manufacturing solutions, from pilot-scale to commercial production. Our expertise includes cell culture, purification, and viral segregation systems. Facilities feature cleanrooms, QC labs, and bio-safety protocols to ensure product integrity and regulatory compliance.
API Production
Ce & Ic designs API manufacturing facilities covering synthesis, filtration, and potent compound containment. Our projects include hazardous material handling systems and compliance with cGMP standards. Clients receive scalable, efficient layouts for kilo-lab to large-scale operations.
Sterile Fill-Finish
Our sterile fill/finish solutions incorporate cleanroom environments and automated production systems. Designs prioritize contamination control and compliance with sterility assurance standards. We support equipment selection, process validation, and facility qualification.
Regulatory Compliance
Ce & Ic provides gap assessments, due diligence, and compliance strategies for FDA, EU, and global markets. Our team ensures facilities meet evolving regulatory expectations through detailed documentation, hazard reviews, and risk mitigation plans.
People
Ed McAvoy
Project Director
With decades of experience, Ed McAvoy leads complex GMP projects, ensuring seamless execution from concept to commissioning. His expertise spans process engineering and client collaboration.
Tony Muratore
Project Director
Tony Muratore specializes in pharmaceutical facility design, focusing on cost-effective, compliant solutions. He brings 20+ years of experience in biologics and sterile manufacturing.
Jim Henry
Senior Project Manager
Jim Henry integrates process engineering and project management to deliver efficient, scalable facilities. He has led numerous API and potent compound containment projects globally.
Questions
What industries does CE&IC specialize in?
CE&IC serves pharmaceutical, biotechnology, and specialty chemical industries with GMP-compliant design solutions.
How long has CE&IC been in business?
CE&IC has delivered engineering and architectural services since 1984, with over 35 years of industry experience.
What regulatory standards does CE&IC follow?
We prioritize US FDA, EU, and international regulatory compliance across all projects, including cGMP and bio-safety standards.
Does CE&IC handle international projects?
Yes, CE&IC works on projects across the United States and internationally, adapting to global market requirements.
What services does CE&IC offer?
Our services include planning, design, consulting, construction assistance, and commissioning for pharmaceutical facilities.
