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Our Solutions
GQT Med Global offers integrated services across the pharmaceutical value chain. Whether you require hard-to-find raw materials, formulation development support, regulatory documentation, or temperature-controlled distribution, our team provides the expertise and infrastructure to meet your needs.
Specialised Sourcing & Distribution
APIs, Excipients & Intermediates
Comprehensive sourcing from market scanning to vendor qualification and performance monitoring. We provide complete documentation packages including CoA, SDS/TDS, specifications, and nitrosamines risk assessments. Our team tracks DMF/CEP status and manages REACH/CLP, TSE/BSE.
R&D & Applications Laboratory
Formulation Development
Formulation prototypes across oral solid dosage, liquids, semi-solids, and topical systems. We conduct QbD/DoE screening for excipient selection, develop and validate analytical methods per ICH Q2(R2), design stability studies following ICH Q1A, and provide scale-up and PPQ support.
Quality & Cold Chain Logistics
GDP-Compliant Distribution
Validated temperature-controlled lanes at 2–8 °C and 15–25 °C with continuous data logging and route-risk assessment. Warehousing with WMS, FEFO/FIFO control, quarantine management, and full recall capabilities. Trade compliance support for all major Incoterms with cargo insurance.
Specialised Sourcing & Procurement
We employ comprehensive market intelligence and rigorous supplier qualification to source APIs, excipients, intermediates, solvents, and specialty materials from vetted manufacturers worldwide. Our dual-source strategies, price discovery processes, and allocation management ensure you have reliable access to the right materials at competitive pricing with full supply security and regulatory compliance.
Materials Covered
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Active Pharmaceutical Ingredients (APIs)
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Excipients (binders, fillers, disintegrants, lubricants, coatings)
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Intermediates and key starting materials
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Solvents and reagents
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Packaging materials (bottles, closures, blisters)
Key Services
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Market scanning and supplier long-listing
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Vendor qualification and performance monitoring
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Dual-source strategy development
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Price discovery and competitive bidding
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Allocation management for constrained materials
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Complete documentation packages (CoA, SDS/TDS, specifications)
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DMF/CEP status tracking and coordination
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REACH/CLP, TSE/BSE, and allergen compliance management
R&D & Applications Laboratory
Our applications laboratory provides formulation prototyping, excipient selection, compatibility studies, and scale-up support across oral solid dosage, liquids, semi-solids, and topical systems. We conduct Quality by Design (QbD) and Design of Experiments (DoE) screening, develop and validate analytical methods per ICH Q2(R2), design stability studies following ICH Q1A, and deliver comprehensive process performance qualification (PPQ) support.
Key Services
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Formulation prototyping (tablets, capsules, liquids, creams, gels)
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Excipient compatibility and selection studies
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QbD/DoE screening and optimization
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Analytical method development and validation (ICH Q2(R2))
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Stability study design and execution (ICH Q1A)
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Scale-up and process transfer support
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Process performance qualification (PPQ)
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Dissolution testing and bioequivalence support
Application Areas
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Oral solid dosage (immediate and controlled release)
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Liquid formulations (solutions, suspensions, emulsions)
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Semi-solid formulations (creams, ointments, gels)
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Topical and transdermal systems
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Nutraceutical and dietary supplement formulations
Quality & Regulatory Support
We maintain an ISO-aligned Quality Management System with ICH Q7 awareness for APIs and EXCiPACT-oriented processes for excipients. Our quality team manages change control, CAPA (Corrective and Preventive Action), and CMC (Chemistry, Manufacturing, and Controls) support for residual solvents (ICH Q3C), elemental impurities (ICH Q3D), and coordinates testing via ISO/IEC 17025-accredited partner laboratories.
Regulatory Documentation
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Drug Master Files (DMF) coordination
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Certificates of Suitability (CEP) management
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REACH/CLP compliance documentation
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TSE/BSE, GMO, allergen declarations
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Halal/Kosher certifications where applicable
Key Services
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ISO-aligned QMS with pharmaceutical focus
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Change control and deviation management
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CAPA (Corrective and Preventive Action) programmes
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Supplier audit coordination (desktop and on-site)
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CMC documentation support for regulatory submissions
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Residual solvents testing and compliance (ICH Q3C)
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Elemental impurities assessment (ICH Q3D)
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Nitrosamine risk assessment and mitigation
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Coordination with ISO/IEC 17025 accredited laboratories
Cold Chain & Logistics
We operate validated temperature-controlled distribution lanes at 2–8 °C and 15–25 °C with continuous data logging, route-risk assessment, and contingency planning. Our warehousing operations employ Warehouse Management Systems (WMS) with FEFO/FIFO inventory control, quarantine and returns management, full recall capabilities, and comprehensive trade compliance support for all major Incoterms with cargo insurance coverage.
Key Services
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Validated 2–8 °C cold chain lanes
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Controlled 15–25 °C ambient lanes
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Continuous temperature data logging
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Route-risk assessment and contingency planning
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WMS-enabled warehousing with FEFO/FIFO control
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Quarantine and returns management
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Full product recall capabilities
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Trade compliance (HS codes, certificates of origin, customs)
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Support for all major Incoterms (EXW, FOB, CIF, DDP)
Logistics Capabilities
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EU/UK distribution networks
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MENA and CEE regional coverage
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Cross-border customs clearance
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Dangerous goods (DG) handling and documentation
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Packaging and labelling services
Custom Synthesis & Manufacturing
We coordinate route scouting, feasibility studies, and cost modelling for custom intermediates and key starting materials. Our network of contract synthesis partners operates under strict confidentiality agreements to deliver bespoke molecules, tolling services, technology transfer support, and impurity control strategies tailored to your development and manufacturing requirements.
Synthesis Capabilities
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Small molecule APIs and intermediates
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Chiral synthesis and resolution
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Peptide synthesis
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Heterocyclic chemistry
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Organometallic reactions
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Hazardous chemistry (high pressure, cryogenic, pyrophoric)
Key Services
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Route scouting and synthetic pathway optimization
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Feasibility studies and cost modelling
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Custom intermediate synthesis
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Key starting material (KSM) production
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Tolling and contract manufacturing coordination
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Technology transfer and process validation
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Impurity profiling and control strategies
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Scale-up from grams to multi-kilogram batches
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Confidentiality and IP protection
Documentation & Compliance Services
We provide comprehensive documentation packages that support regulatory submissions, supplier qualification, and ongoing compliance monitoring. Our team coordinates with manufacturers to ensure all technical data sheets, certificates of analysis, regulatory status updates, and change notifications are current, accurate, and aligned with global pharmaceutical standards including EMA, FDA, and ICH guidelines.
Key Services
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Complete technical documentation packages
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Certificate of Analysis (CoA) verification
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Safety Data Sheets (SDS) and Technical Data Sheets (TDS)
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Specification sheets and test methods
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DMF/CEP status tracking and updates
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Change control notifications
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Regulatory status reports (EMA, FDA, WHO)
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Pharmacopoeial compliance (Ph. Eur., USP, JP)
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REACH/CLP registration and compliance
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Nitrosamine risk assessment documentation
Compliance Areas
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ICH guidelines (Q3C, Q3D, Q7, Q1A, Q2(R2))
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GMP/GDP compliance
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Pharmacopoeial standards
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Environmental regulations (REACH, RoHS)
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Trade compliance and export controls
Raw Materials Portfolio
Sourcing and supply of active pharmaceutical ingredients across therapeutic categories including cardiovascular, CNS, anti-infectives, oncology, gastrointestinal, respiratory, and endocrine. Available in technical, pharmaceutical, and compendial grades with DMF/CEP support, CoA, and full impurity profiling per ICH Q3A/Q3B.
APIs
Comprehensive range of pharmaceutical excipients including binders (PVP, HPMC, cellulose derivatives), fillers (lactose, MCC, starch), disintegrants (croscarmellose, crospovidone), lubricants (magnesium stearate, stearic acid), coatings (Opadry, shellac, cellulose acetate phthalate).
Excipients
Custom and catalog intermediates for API synthesis, key starting materials (KSMs), building blocks, and specialty chemicals. Available with full synthetic route documentation, impurity specifications, and regulatory support for backward integration and supply chain security.
Key Starting Materials
Pharmaceutical-grade solvents (ethanol, methanol, acetone, IPA, acetonitrile, DCM, THF) and reagents meeting ICH Q3C residual solvent limits, with batch-specific CoA, GC/HPLC purity data, and compliance with Ph. Eur./USP monographs.
Solvents & Reagents
Niche and high-value materials including controlled-release polymers, taste-masking agents, solubilizers, penetration enhancers, stabilizers, antioxidants, preservatives, and novel excipients for advanced drug delivery systems.
Specialty Materials
Primary packaging components including HDPE/PET bottles, child-resistant closures, blister foils (PVC, PVDC, Alu-Alu), desiccants, and secondary packaging materials with extractables/leachables data and regulatory compliance documentation.
Packaging Materials
