Please join Element at Contract Pharma Sept. 22-23, 2022, at the Hyatt Regency, New Brunswick, NJ.
Element’s comprehensive pharmaceutical Research and Development (R&D) services help bring your products to life more effectively, get them to market faster and save time and money throughout your development and production processes.
As a fully Good Manufacturing Practice (cGMP) compliant laboratory, Element offers the full spectrum of product and process development, testing, failure analysis and consulting services in a broad range of technology areas.
About the event
The Contract Pharma Exhibition will be held at the Hyatt Regency New Brunswick, NJ, located in the heart of New Jersey’s pharmaceutical industry. The two-day conference and one-day exhibition on September 22 provide the perfect venue for easy, informal discussions for manufacturing, packaging, laboratory services and more.
Book a meeting
Schedule a meeting with one of our experts to learn more about how we can help you to develop better products, save time and money, and minimize potential risk to your business.
The Industries We Serve
Our Environmental Monitoring programs allow pharmaceutical manufacturers and compounders to measure and monitor cleanliness and contamination levels within their facilities.
We provide USP <797>, USP <800> and cGMP FDA compliance expertise and testing solutions for home infusion, pharmacies, hospital pharmacies and human drug outsourcing facilities
Biopharmaceuticals and Biologics Analysis
Element’s significant expertise in all stages of biologics R&D, from in-house protein biochemistry and molecular biology to cellular biology and QC experience, supports the entire product development life cycle.
Extractables and Leachables Studies
Element's extractables and leachables studies offer tailored solutions that ensure patient safety and compliance with industry standards.