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Pharmarama delivers operational excellence in the global supply of comparator drugs for your comparator study. We are a leading global clinical trial supplies company that specializes in providing validated comparator sourcing services with speed, accuracy and the highest degree of ethical standards. With offices in the UK and US, and partnerships in Germany and China, we are ideally located to serve local and global requests, with the knowledge and expertise to source the comparators you require when you need them. Procurement of a specific comparator drug for a global clinical trial is a complex process. As a fully integrated organization, we offer a single point of contact for sourcing and distribution of comparator supplies on a worldwide basis. Sourcing and ProcessComparator drug procurement directly from the manufacturer when appropriate, supplying large single batches with maximum shelf life Audited world-wide suppliers ensuring integrity of the supply chain and the ability to comply with the most challenging of drug sourcing requests Licensed by the Massachusetts Board of Registration of Pharmacy for our Wholesale Distributor’s Permit and a Wholesale Distributor’s Controlled Substance Permit. Certified by the United States Department of Justice Drug Enforcement Agency for the distribution of Controlled Substances. Licensed by the MHRA (Medicines and Healthcare products Regulatory Agency) and UK Home Office to store and supply controlled drugs Members of the Royal Pharmaceutical Society of Great Britain and Institute of Clinical Research
Team of on-site pharmacists Operate with complete confidentiality
Supply Chain ManagementOur supply chain systems are audited and approved by customers, including major pharmaceutical companies, clinical research organizations and clinical trial packaging companies Extensive cold chain expertise (2°-8°C) with world-wide delivery capability Robust set of SOPs to ensure complete compliance to GDP (Good Distribution Practice) Dedicated Quality Assurance Department Provide Certificates of Analysis and Certificates of Conformance where available Regulatory expertise and understanding of EU Clinical Trial Directives Track documentation from source to trial site
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