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Dalton Pharma Services

Dalton Pharma Services is listed as a small business research supplier in the Scientist.com network, with 1 site in 1 country and 2 service areas.

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Sites 1
Countries 1

Services

What this research supplier says it provides, as listed in the Scientist.com network.

Type of company: Small business

Chemical and Compound Analysis

  • Impurities in API Risk assessment Create a risk-based control strategy to determine any impurities in Active Pharmaceutical Ingredients (API).
  • Structural Chemistry Examine the relationship between protein structure and function.

Chemistry, Manufacturing and Controls (CMC)

  • API and Drug Product Stability Testing API and Drug Product Stability Testing.
  • API and drug product storage and release API and drug product storage and release
  • API manufacturing process development, tech transfer and validation API manufacturing process development, tech transfer and validation
  • API Stress Testing Studies Develop analytical methods to predict stability problems and identify degradation products/pathways under forced degradation conditions.
  • API/ Excipients Compatibility Studies Delineate real and possible interactions between potential formulation excipients and the API as an important risk reduction exercise early in formulation development.
  • Chemistry, Manufacturing and Controls (CMC) Request Chemistry, Manufacturing and Controls services
Show all 15 in Chemistry, Manufacturing and Controls (CMC) 9 more
  • Drug Formulation Combine substances including the active drug into a final product with the desired metabolic and therapeutic properties.
  • Drug product packaging and labeling Drug product packaging and labelling
  • Drug Substance and Drug Product Characterization and Manufacturing Drug Substance and Drug Product Characterization and Manufacturing.
  • Fill and Finish Processing Confirm final product sterility, formulation and packaging in the biopharmaceutical process.
  • Forced Degradation Run light, heat, humidity, acid hydrolysis and oxidation tests to evaluate substance degradation.
  • Formulation Services Assistance when determining the look, texture, fragrance of a product with compatibility with product packaging, knowledge of competitive performance traits and product shelf life.
  • GMP Synthesis Synthesize APIs including small molecules, formulations and protein-based drugs under GMP compliance.
  • ICH-compliant stability testing Perform ICH-compliant stability testing
  • Powder Filling Use manual, automatic or semi-automatic machinery to package a variety of powder and granules.

Discovery Chemistry

  • Building Blocks Find chemicals used for creating new compound chemotypes and HTS libraries.
  • Compound Synthesis Synthesize small molecule candidates for use in hit followup, lead optimization and medicinal chemistry.
  • Custom Building Blocks Find or synthesize mg to kg amounts of chemical building blocks, scaffolds and reactive intermediates.
  • LCMS Analysis Physically separate substances using liquid chromatography and mass spectrometry.
  • Leachable and extractable testing Leachable and extractable testing
  • Lead Optimization Perform chemical structural changes to improve preclinical drug candidate.
Show all 7 in Discovery Chemistry 1 more
  • Structure Activity Relationship (SAR) Analyze the relationship between the structure of a compound and its biological activity.
Show all 35 services 21 more

DNA & RNA

  • Oligo Synthesis Produce oligonucleotides for microarrays, RT-PCR and PCR cloning.

Drug Development

  • Chemistry, Manufacturing and Controls (CMC) Consulting Consultant services related to the development of pharmaceutical and biopharmaceutical drug products that are consistently effective, safe and high quality for consumers.
  • Medicinal Chemistry Consulting Apply chemistry training to the process of synthesizing new pharmaceuticals.

In Vitro ADME

  • Isotopic Labeling Track labeled isotopes through a metabolic pathway or cell by measuring mass, vibrational mode or radioactive decay.
  • Metabolite Synthesis Synthesize drug metabolites that are formed after administration of drug to an animal model or patient.
  • Reference Standards Find reference standards for assays, tests and services.

In Vivo Pharmacokinetics

  • Mass Balance Elucidate excretory pathways and organ distribution of a parent drug and metabolites

Nanotechnology

  • Drug Delivery Technology Create microstructures that enhance drug metabolism properties.
  • Liposomes Create artificial spherical vesicles that can be used as a vehicle for administration of drugs.
  • Nanoparticle Conjugation and Functionalization Modify biomolecules to enhance structure and function.
  • Nanoparticle Synthesis Create nano-level structures with unique features.

Service areas:

Chemistry Manufacturing

Source: Scientist.com supplier network

Where it operates

Sites by country, with the cities in each.

  • Canada North York 1 site

Source: Scientist.com supplier network (site locations)

About this supplier

In the supplier's own words, as listed in the Scientist.com network.

Dalton Pharma Services is a leading provider of integrated cGMP chemistry, drug development and finished dose manufacturing services to the pharmaceutical and biotechnology industries. Our integrated approach allows Dalton to optimize development and manufacturing in parallel tracks where possible, saving our customer’s valuable time and resources. The result is fully optimized and scalable processes, producing high quality products meeting customer timelines. Dalton operates modern 42,000 square foot (3,900 square meter) cGMP facilities, centrally located in Toronto. Our cGMP facilities...

Show the full description

Dalton Pharma Services is a leading provider of integrated cGMP chemistry, drug development and finished dose manufacturing services to the pharmaceutical and biotechnology industries. Our integrated approach allows Dalton to optimize development and manufacturing in parallel tracks where possible, saving our customer’s valuable time and resources. The result is fully optimized and scalable processes, producing high quality products meeting customer timelines. Dalton operates modern 42,000 square foot (3,900 square meter) cGMP facilities, centrally located in Toronto. Our cGMP facilities have recently undergone upgrades including new vial washing, depyrogenation, fill line RABS, HVAC systems, as well as a new WFI system.
We’ve also just added Steriles made Simple℠ programs which can bring your sterile liquid injectables to the clinic even faster.
Our customers range from the smallest start-up biotechs to global pharmaceutical companies. Dalton offers integrated services supporting R&D through to small scale commercial manufacturing, all in one company,We bring more than 25 years of experience to every customer project.
Dalton offers chemistry, API and finish dose services for research and cGMP requirements. Our chemistry services cover a wide range of molecule and reaction types. These services are fully supported by Dalton’s in house analytical services, which can characterize your molecule and provide analytical development, validation, release and stability services. Our services include:
• Medicinal Chemistry
• Custom Synthesis and Process Development
• cGMP API (bench top to multi-kg scales)
• Formulation Development
• Analytical Services
• cGMP Sterile liquid, lyophilized and powder dosage forms (vials)
• cGMP Powder filled capsules – solid oral
The Dalton Research Molecules business carries over 2,000 standards, building blocks, metabolites and impurities in its growing catalog available for direct purchase.
Discover, Develop, and Manufacture with Dalton.

Website
www.dalton.com

Source: Scientist.com supplier network, written by the supplier

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Sources: Scientist.com supplier network.

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