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www.corerxpharma.com
CoreRx, Inc OverviewOur Core Business
CoreRx, Inc. is a Dosage Form Development company specializing in formulation development, analytical development and clinical manufacturing of various dosage forms
• Drug Characterization
• Preformulation
• Formulation Development • Analytical Development
• Clinical Trial Materials Manufacturing
Our Core Focus
• Complete client satisfaction
• Highest quality science
• Consistent and effective communications
• Strong timeline management
• Full attention to client goals at all levels
Why CoreRx?
• People and ExpertiseIt all boils down to people and trust..
• CommunicationEffective, Scientist-to-Scientist communication is the cornerstone to every CoreRx™ project’s success.
• FlexibilityCoreRx™ scientists, management, and systems ensure flexibility and agility, allowing for direction changes without inflexible systems and bureaucratic hassles.
Why CoreRx?• Speed
CoreRx™ understands that developing innovative solutions for improved patient care, combined with the bottom line, revenues and profitability, are tied to getting your product on the market as quickly as possible.
• EducationAffiliation with Univ. of South Florida as Center for Advanced Pharmaceutical Learning. Students will learn hands-on techniques in industrial pharmaceutics from member of CoreRx team who are Associate Faculty at USF.
• Quality systemsDocumentation, quality, and operational systems are a necessity in a GLP/cGMP environment. Quality & timeliness must go hand in hand.
Why CoreRx…?
• Oh yes… and Location
Executive/Scientific Team
• Todd R. Daviau, Ph.D. - Chief Executive Officer– 25+ years of pharmaceutical experience – Director of the Analytical Group for MDS Pharma Services– Guilford Pharmaceuticals (GliadelTM)– Nova (later Scios) Pharmaceuticals
• Brian McMillan, Vice President, Formulation Development– 20+ years of experience in pharmaceutical formulation development– MDS Pharma Services– Bausch and Lomb Pharmaceuticals– Roxane Laboratories
Executive/Scientific Team
• Mark J. Licarde, Vice President, Technical Operations– 28+ years in pharmaceutical manufacturing – MDS Pharma Services – Mylan Pharmaceuticals– Bristol Myers Squibb
• Jim Davis, M.S., Vice President, Business Operations– 16+ years of pharmaceutical experience– MDS Pharma Services– Bausch and Lomb– Proceutics / Oread
History
• Founded in 2006
• Started with 5 employees
• Now at 41 employees
• Grown from 3300 sq. ft. to over 35,000 sq ft.
CoreRx’s Convenient Location
Clearwater, Florida~15 minutes to Tampa Airport (TPA)
cGMP Compliant
FDA/FL DOH Registered
DEA LicensedSchedule II - V
Insert new map
CoreRx Facility Overview
• Approximately 35,000 square feet• 19 Manufacturing suites13 cGMP – including 1 for special projects (low RH, low light, etc.)6 Non-GMP – formulation development • Manufacturing capacity – up to ~500kg• Expanded laboratory space:•Formulation Development•cGMP Manufacturing•Stability storage testing•Analytical
•R&D•cGMP
New LocationFormulation Suites
Analytical Labs
Warehouse
cGMP ManufacturingArea
Admin areas
Core Competenciesby Business Unit
• Preformulation Services– Drug substance characterization
• Analytical Services– Method Development and Validation
• Formulation Development– Liquids, Semi-solids and Solids
• Manufacturing, Packaging & Labeling– API in Capsule or in Bottle– Liquids, Semi-solids and Solids– Matching Placebo manufacture– Blinding of reference product (over-encapsulation)
• Stability Program Management– ICH or customized stability parameters
Additional Capabilities
• CoreRx is committed to adding innovation where we see a client need– API in capsule/bottle services
• Xcelodose ®• Quantos®
– Multi-layer tablet (up to 3 layers)• FlexiTab ®
– Liquid in capsule services– Multi-particulate capsules
• CoreRx licensed with DEA– Controlled substances (II – V)
• Overencapsulation services – comparator or “blinding” studies
Project Management/Logistics
• Project Manager is assigned to manage:– Project planning and Execution– Team leadership with integration of technical– Manage all CoreRx-Client communications
• Project Teams are made up of subject matter experts which represent their respective disciplines:– Project Management/Logistics– Analytical Chemistry– Formulation Development– Manufacturing– Quality Assurance
SERVICES
Preformulation
Preformulation CharacterizationSolid and/or Solution Characterization can be Conducted Utilizing the Following
Instrumentation/Procedures:• Thermal evaluation
• DSC, TGA, Hot-stage microscope• FTIR• X-ray Diffraction• Particle size/morphology• Polarized microscopy• Moisture content
• KF, moisture analyzer• Moisture sorption profile• pH solubility • Partition coefficient• Photostability• Intrinsic dissolution
Analytical Services
Experienced Professionals in Analytical Chemistry• Method Development, Qualification and Validation
• HPLC, uPLC, Dissolution, etc.
• Raw Material Testing (select)• Stability Sample Analysis• Dissolution Testing• Chiral Analysis• Cleaning Analysis/Verification• CMC Technical Packages
Analytical Services
• Analytical Support for Formulation Development• Stability and QC Release Testing• API/Reference Standard Characterization• Isolation and Identification of Impurities• Physical Chemistry
Formulation Services
• Solids• Tablets, Capsules, Modified Release, Coatings
• Semi-Solids• Creams, Gels, Ointments, lotions, etc.
• Dispersed Systems• Emulsions & Suspensions
• Liquids• Oral, Ophthalmic, Parenteral
Formulation Services
Solid Oral Capabilities• API in Bottle/Capsule• Excipient Compatibility• Oral Drug Delivery
• Tablets, Capsules, Powders, Pellets, Mini-Tablets• Solutions, Suspensions, Emulsions, Powders for Reconstitution
• Solid Dispersions• Lipid Formulation Delivery for Poorly Soluble/Bioavailable APIs• Multi-Phasic, Extended and/or Delayed Release Drug Delivery• Highly Potent Compounds
Contract Manufacturing Services
• Manufacturing– API in Capsule/Bottles– Tablets, Capsules, Pellets, Mini-Tablets– Liquid in Capsule
• Solutions, Suspensions, Emulsions
• Over-Encapsulation, Reference Product Blinding • Packaging & Labeling
• Other Services– Matching Placebo Manufacturing– Technology Transfer
Stability• ICH Conditions
– 25oC/60%RH, 30oC/65%RH, 40oC/75%RH– Custom conditions also available
• Protocol design• Report generation• Stability software management system
– SLIM/SLIMStat
• Sample analysis• Secure storage
Why CoreRx…?
• Quality First Focus– Numerous audits reinforcing compliance
• Responsiveness– Flexible manufacturing model– Unique project management team structure with client-centric focus– Cross training program for employees
• Technology– Investment in new equipment and expertise as they become available
• Expertise– Ability to attract top-level talent with high-level benefits package
• Reliability– Leveraging our company’s size to your advantage
Faster to Clinic with Xcelodose ® or Quantos®
• Manufacturing– Advanced neat drug dosing directly into capsule or bottle– Decreases lab to clinic development– Decreases API requirements– Decrease risk of stability– Minimizes API waste
…and now even Faster to Clinic with ClinicFirstSM 60Day Guarantee
• The CoreRx ClinicFirst program is designed for clients requiring rapid supply of clinical trial materials for First-in-Man (Phase I) clinical studies.
• API in Capsule• Blend in Capsule• API in Bottle• Blend in Bottle
Introducing SuiteViewTM…
• Formulation & Manufacturing– Real-time video feed (Pan, Tilt & Zoom)– Remote/IP access
• Password controlled
– Two way communication• Reduce travel time/costs
Choose CoreRx
The projects we work on may change....
our values won't...
quality, reliability, value, integrity
www.corerxpharma.com