Capabilities
Ancillare provides end-to-end clinical trials process management services to pharmaceutical, biotechnology, CRO and research medical organizations. Our mission is to maintain the integrity of the global biopharmaceutical supply chain to preserve human life and promote effective scientific discovery. Our proven approach provides a dynamic partnership to assist our clients in their efforts to achieve protocol success. Through our partnership, Ancillare can build efficiency and global accountability while reducing time to market and cost of managing clinical trials of any size or specialty.
Methodology
Flexibility and accuracy are essential to meet the demands of modern protocols. At Ancillare, our model is designed to provide both to our partners. First, our unique flexible staffing model allows our clients to maintain lean operations and expertise networks to develop an effective clinical trial process. Our Ancillare Professional Teams can be configured as fixed groups for our customers or can be provided on an as needed basis to balance project developments. We are able to leverage our proven supplier network to achieve cost-effective clinical trials with partners that can provide services on a JIT basis. Our comparator and clinical services ensure authenticity and proven effectiveness at a global level. Lastly, our regulatory and logistics expertise allows us to create clinical trial supply chains proven to perform and meet local and regional requirements. Our model works with clients from pre-protocol development to post-last patient out in order to create the centralized partner needed to manage modern protocol complexity. Whatever the size or scope of your protocol requirements, Ancillare can build a program to exceed your clinical requirements.
Services
Highlights
 |
Dynamic Partnership with Merck: Ancillare was the first supplier featured on www.merck.com. Read the article about Ancillare on merck.com.
|
|
Major Pharmaceutical Contracts: We have been selected as preferred suppliers to several major pharmaceutical companies to help manage their clinical trial process.
|
|
Large Trial Management: Ancillare holds expertise in helping to conduct large clinical trials across developing regions. Our teams have helped manage clinical supply chains and build infrastructure necessary to conduct some of today’s largest protocols.
|
|
Small Project Expertise: Ancillare has succeeded in fulfilling the most specialized protocol requirements. From providing clinical materials labeling activities to helping manage stage I and II clinical trials, Ancillare has the expertise needed to meet challenging demands.
|
|
Emerging Market Expertise: We were awarded the 2010 US Department of Commerce’s Export Achievement Certificate for our logistical expertise in emerging markets and global distribution management. Our expertise can help with multinational protocols of all sizes.
|
|
Drug Distribution Expertise: Ancillare has been awarded a DEA Class II-V license to distribute drugs to clinical sites and service providers around the world. Our experience can fulfill comparator services for global protocols and individual projects alike.
|
|
Large Storage Facilities: Ancillare has an ISO Class 8 Clean Room facility, drug storage vaults, cold storage areas and a large ambient warehouse facility at our North Wales Pa location to meet any protocol requirement. Our facilities have passed numerous Quality Assurance Audits including DEA and top-five pharmaceutical inspections.
|
|
Software Platforms: Ancillare has unique software solutions to track the clinical process from start to finish including proprietary ERP and ARDMS dashboard systems for our partners. Our systems are compatible with all current corporate software packages |
