Our History
BioPharm Match was founded in 2002 on the simple premise that service providers around the world could use an insider's help in cultivating business opportunities with US sponsors. Our strategy was to identify top notch resources and to broker the best possible relationships for our portfolio of client companies.
We quickly discovered that our simple notion was on the cutting edge of a major trend in the life science industry - international outsourcing. Mindful of this, we broadened our scope to offer services to sponsors with specialized needs in various therapeutic areas, in study designs, in geographic placements, and in accessing unique patient populations and demographics. What we found was a vibrant and receptive market for these services, and we have continued to grow and expand scope ever since.
The Right CRO...Right Now!
We now provide sponsors with fast, easy access to leading specialty CRO's and CSO's in virtually every country of the pharmaceutical world. All of our service providers are pre-qualified based on stringent criteria including GCP/GLP, FDA audits, financial stability, past performance, and strong, sound management. With every project we undertake, we stake our professional reputation on the results produced by the service providers we recommend.
We are proud to offer service providers in the following areas:
· Analytical Facilities: We can help sponsors select the analytical lab ideally suited for the needs for method development, biomarkers, genomics, bio-analytical work, pharmacopeia testing, and more.
· BA-BE CRO's: We do lots of work in the BA-BE area, assisting generic drug manufacturers from around the work save millions of dollars and months of time in their clinical programs. Most of our BE work is done in India, although we have relationships with BE CROs in China, South Africa, Canada, USA, Phillipines, Australia, and across East and West Europe.
· Consultants: Finding the right consultant who has "been there, done that" is not always easy. Although we do not claim to know all the consultants in the world, we know a lot of them, and can make fast and complete introductions.
· Central Labs and Clinical Supply Services: Provide the details of your project and we will provide a list of service providers to meet them.
· Data Management:We routinely work with leading data management companies in North America, India, Europe, South America and South Africa.
· Non-Clinical: Animal models, toxicity, BA studies
· Phase 1 - 2a: First-in-Man, ADME, C14, QTc, Dose Finding, Drug-Drug Interaction, Food Effect, Hepatic Impaired, Renal Impaired, Oncology, Healthy Obese, and a wide range of patients/subjects.
· Phase 2 - 4: We know the therapeutic experience and expertise for most of the CROs around the world. We understand their access to investigators and patient populations, thereby saving sponsors significant time and energy to discover this information on their own.
· Regulatory Consultants: Whatever your regulatory needs, in any country in the world, we can assist you. From simple clinical trial applications to complex multi-country license submissions, we can identify the Regulatory Consultant for you.
