Element’s pharmaceutical method development and research services bring your products to life...for life.
Creative outsourcing of your drug development and manufacturing activities can help your organization bring new products to market in a timely and cost-effective manner. An effective partnership with a strong contract research organization can produce continued striking results.
Element delivers proficient pharmaceutical development services supporting all stages of product development, manufacturing, and post-market testing.
Our scientists thrive on problem-solving and are regularly presented with complex challenges. Our engineers and chemists are ready to collaboratively review and discuss historical data with your technical team and develop an effective approach to investigate your key issues.
Flexibility and communication
Our Engaged Experts begin working on your project with an initial consultation to ensure that we fully understand your needs. We deliver proposals with clearly stated objectives and deliverables. An experienced project manager will coordinate your activities and ensure that you receive regular progress updates.
The Element advantage
Element’s ability to assemble a comprehensive team from a variety of scientific disciplines creates a competitive advantage for our clients. Solutions are developed more quickly and efficiently, cost redundancies are eliminated, and clients reduce the time spent in locating, screening and coordinating multiple vendors. With our flexible approach, we can facilitate audits and inspections at your convenience.
For more information about our pharmaceutical method development and research services or to request a quote, contact us today.
Pharmaceutical Stability Storage and Testing
Element offers advanced pharmaceutical stability testing and ICH storage services to ensure the maintenance of product quality, safety and efficiency throughout the shelf life.
Pharmaceutical Research and Development Services
Element provides a comprehensive range of pharmaceutical research and development services to deliver accurate results while reducing cost and time to market.
Residual Solvents Testing – USP 467 and ICH Q3C
Element’s residual solvents testing services per USP 467 and ICH Q3C ensure product quality and safety.
Analytical Method Development and Validation
Element provides innovative analytical method development and validation solutions to regulatory guidelines for a wide range of analytical technologies.
Forced Degradation Studies
Element’s forced degradation, stress testing services per ICH Q1A guidelines assess the stability of drug substances or drug products with effects on purity, potency, and patient safety.
More from Element
CMC Product Development
Our CMC product development services include formulation development, parenteral and topical product development, microbiology testing services, and consultancy.
Excipient Raw Materials and Container Testing
Element has comprehensive capabilities that can be applied to the testing of excipient, raw materials, and pharmaceutical containers, enabling you to ensure the quality and safety of your product.
Discover blog posts, articles, white papers, webinars, and advice from our world-leading testing, inspection, and certification experts.
Local laboratories, global platform
Doing business with one of our laboratories enables our clients' access to our global platform of expertise, capacity and capabilities.