Magellan's Synthesis division is a reliable and knowledgeable resource for both non-GMP and GMP synthesis of your pharmaceutical target compounds. Our experienced team uses either sponsor-defined or innovative chemistries to prepare your requested compounds in milligram to kilogram quantities to meet your specifications.

By working with us, you can shorten timelines to key milestones, support your ever-growing pipeline while holding fixed costs steady. We can assist you in evaluating new technologies and product venues without you committing staff and resources prematurely, as well as help you maintain tight schedules by completing activities in parallel with your internal R & D.

Please give us a call with any questions or submit a project to us for price quotation online.

Synthesis Capabilities

Non-GMP and cGMP synthesis including:

• New Chemical Entities
• Analogs/SAR Families
• Magellan's "Peak Purity" Analytical Standards
• Pharmaceutical Intermediates
• By-Products
• Degradants
• Metabolites
• Isotopically Labeled or "Tagged" Compounds
• PEG Derivatives
• Prep. HPLC and Freeze Drying Capabilities
• Process Development and Scale-up
• cGMP Synthesis of Early Clinical Trial Actives
• Technical Reports/Regulatory Documents
• Technology Assessment
• API Release Testing

Services Offered By Magellan

• Analytical Testing
• Bioanalysis
• Biotechnology
• Clinical Packaging
• Compendial Analysis
• Drug Discovery & Bioassays
• Drug Substance Testing
• Inhalation Product Development
• Method Development and Validation
• Microbiology
• Pharmaceutical Synthesis
• Pharmaceutical Validation
• Pharmaceutics
• Quality Assurance Consulting
• Regulatory Affairs
• Stability Storage
• Stability Testing
• Structural Chemistry