Meet with Element's world-renowned Engaged Experts at the CPhI North America Conference April 30-May 2 in Chicago, IL. Find out about our latest CMS product development & testing, clinical manufacturing, explore our discoveries in drug products delivery and secure your future partnership with us.
About the event
CPhl is an established pharmaceutical event offering fantastic opportunities to network with over 7,400 attendees, connect with Pharmaceutical players from over 40 countries and learn the latest industry trends at more than 110 hours of educational content.
有关该活动的更多信息here.
Why attend?
Element Wilmington (previously known as Exova SL Pharma), is fully GMP compliant manufacturing and testing facility and has been providing high value and high-quality pharmaceutical CMC product development and quality control testing services focused primarily on parenteral, ophthalmic, intranasal and topical drug products, since 1997.
Element’s pharmaceutical and biotechnology industry leaders, Dr. Pramod Nednoor, Kalyan Potluri and Dr. Jim Scull, VP of our Health Sciences Division will be on hand to discuss end-to-end testing solutions specific to your project needs.
Pramod and Kalyan, based in our Wilmington DE laboratory will be available to provide expert advice on formulation development and full CMC services including Preformulation, CMC and clinical manufacturing services for Parenteral, Ophthalmic, Topical and Oral solutions.
Dr. Jim Scull is a well-known expert and author on extractables and leachables programs and will be meeting with interested firms to discuss their particular project requirements.
Take this opportunity to drop by ourBooth #1614and meet our experts for consultation.
Book a Meeting Today!
Schedule a meeting with one of our Engaged Experts to discuss Element’s comprehensive range of services offered to the Pharmaceutical industry, including:
- Full CMC Product Development of both Innovative and Generic Drug Products
- Manufacture of Tox, Phase 1 & Phase 2 Clinical Batches
- Characterization of molecule and Pre-formulation studies
- pH/Solubility and Excipients Compatibility studies
- Formulation Development studies
- Full analytical and microbiological support for the above
- 对容器/封闭系统的评估和选择（小瓶和注射器）
- Development and selection of Process and key parameters
- Development of Master Batch Records
- QC release and stability testing of marketed products
- Tech Transfer & Regulatory Documentation (IND, NDA, ANDA)
Medical Device
作为全面的测试合作伙伴，您将享受单个供应商来源的益处，从机械测试和环境模拟到EMC和无线设备测试。
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Microbiological Analysis
Element provides a wide range of microbiological analysis projects for medical devices, from pathogen and bioburden testing to endotoxin and cytotoxicity analyses.
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乐动LOL
发现博客文章,文章,白皮书,webinars, and advice from our world-leading testing, inspection, and certification experts.
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Local laboratories, global platform
Doing business with one of our laboratories enables our clients' access to our global platform of expertise, capacity and capabilities.
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