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Contract Service Directory
Dalton Pharma Services
Company Headquarters
349 Wildcat Rd.
Toronto, ON M3J 2S3
Canada
Contract Service Directory
- 505(b)(2)
- Accelerated Stability Studies
- Analytical Laboratory Services
- Analytical Methods Development
- Analytical Validation Studies
- Aseptic Processing
- Assay Development
- Biologics Manufacturing
- cGMP Synthesis
- Chemical Analysis
- Chemicals and Raw Materials
- Chemistry, Combinatorial
- Chemistry, Medicinal
- Chiral Separations, R&D
- Clinical Trials, Phase I
- Clinical Trials, Phase II
- Clinical Trials, Phase III
- Clinical Trials, Phase IV
- CMC (Chemistry, Manfacturing & Controls)
- Contract Development and Manufacturing Organization (CDMO)
- Contract Manufacturing
- Contract Research
- Custom Manufacturing
- Custom Protocols
- Custom Synthesis
- Dosage Form Development
- Drug Development Services
- Drug Discovery Support Services
- Excipients
- Expert Testimony
- Filling, Capsule
- Filling, Vial
- Forced Degradation Studies
- Formulation Development
- Formulation Services
- Formulation, Controlled Release
- Lipids/Phospholipids
- Lyophilization
- Manufacturing, Antibody-Drug Conjugates
- Manufacturing, API
- Manufacturing, Aseptic Fill/Finish
- Manufacturing, Biologics
- Manufacturing, Capsules
- Manufacturing, Clinical Trials Supply
- Manufacturing, Controlled Substances
- Manufacturing, Custom
- Manufacturing, Dose Form, Non-Sterile
- Manufacturing, Dose Form, Sterile
- Manufacturing, Ethical
- Manufacturing, Generics
- Manufacturing, Injectables
- Manufacturing, Liquids
- Manufacturing, Lyophilized Products
- Manufacturing, OTC
- Manufacturing, Other
- Manufacturing, Parenterals, Large Volume
- Manufacturing, Parenterals, Small Volume
- Manufacturing, Powders, Non-Sterile
- Manufacturing, Powders, Sterile
- Manufacturing, Solid Dosage
- Manufacturing, Solutions & Suspensions
- Manufacturing, Sustained Release
- Manufacturing, Syringes, Pre-filled
- Manufacturing, Tablets
- Manufacturing, Vaccines
- Manufacturing, Veterinary
- Mass Spectrometry
- Medicinal Chemistry
- Methods Development
- Methods Validation
- Microbiological Testing
- Nonclinical Research
- Packaging, Clinical Trial Materials
- Parenterals Development
- Parenterals, Syringe Filling
- Parenterals, Vial Filling
- Photostability
- Physical Testing
- Pilot-Scale Filling
- Preclinical Testing Formulations
- Preformulation
- Process Characterization
- Process Development/Scale-Up Services
- Process R&D
- Process Validation Studies
- Purification
- QA/QC
- Quality Control Testing
- R&D Services
- Raw Materials Analysis
- Scale-Up
- Stability Studies
- Stability, ICH
- Sterile Filling
- Syringe Filling
- Validation, Filtration
- Validation, Manufacturing
- Validation, Services
- Wet Chemical Analysis
Content From Dalton Pharma Services
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Towards Equitable Risk Relationships
Views on Risk Sharing in Sponsor-CMO ContractsWhite Papers / Tech Papers Released on 11.26.2013
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Breaking News | Industry News | Laboratory Testing
Dalton Pharma Services Expands Capabilities
Offers extractables and leachables testing services.Contract Pharma Staff 11.10.20
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THE CENTRE FOR CELL AND VECTOR PRODUCTION (CCVP)
A Transparent and Flexible Approach to Manufacturing
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Breaking News | CRO News | Promotions & Moves
Parexel Adds Experts to Regulatory Consulting Group
Four new hires from U.S. FDA and MHRA will serve as technical vice presidents12.10.19
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Breaking News | Drug Development | Trials & Filings
SK Bio Gains FDA Approval for XCOPRI
Marks the first time a Korean company has independently brought a compound from discovery to U.S. FDA approval11.25.19
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When Life Gives You Lemons…Raise Your Drug Prices
The hidden effect of economic models on global drug supply and shortages.Ben Locwin 11.20.19
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Biologics, Proteins, Vaccines | Biosimilars
Biopharma Over 20 Years
A look at the key trends that have impacted the biopharma industry over the years.K. John Morrow, Jr. and Eric S. Langer, BioPlan Associates 11.20.19
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cGMP Manufacture | Drug Development
Contract Pharma’s 20th Anniversary Series: CDMO Insight
JoyL Silva of Pfizer CentreOne discusses global market and regulatory changes driving drug development strategies and the evolution of CDMO services and ops.Kristin Brooks, Contract Pharma 11.01.19
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How Can a Contract Development and Manufacturing Organization Advance a Cell & Gene Therapy Product?
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Regulatory Affairs
Quality Metrics Feedback
A look at FDA’s Quality Metrics Initiative, a complicated issue for all of pharma stakeholdersGil Roth, President, Pharma & Biopharma Outsourcing Association 09.16.19
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Breaking News | Clinical Trials | Industry News | Inspections | QA/QC
FDA Extends CRADA with CluePoints
Aims to further explore a data-driven approach to quality oversight in clinical trials09.11.19
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Drug Development | Trials & Filings
Roche Wins Two Approvals for Cancer Drug Rozlytrek
Becomes third tumor-agnostic drug to win FDA Approval08.16.19
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Industry News | Inspections
Dalton Pharma Services Completes PAI Inspection
Paves way for Dalton to manufacture commercial API products for U.S. distribution05.02.19
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Breaking News | cGMP Manufacture | Collaborations & Alliances | Fill/Finish
Dalton, ExCellThera in Devt. and Mfg. Pact
Dalton will be responsible for the formulation and fill/finish of ExCellThera's lead candidate UM17111.26.18
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Aseptic Processing | Fill/Finish | Industry News
Dalton Invests in Automated Sterile Liquid Filling System
Allows larger batch sizes, a broader range of filling volumes and container closure systems09.11.18
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Bio News | Breaking News | cGMP Manufacture | Industry News
Dalton Pharma, Arch Biopartners in Mfg. Tie-up
Dalton to perform the GMP campaign for Metablok08.17.18
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Dalton Receives Compliant Rating from Health Canada
Inspection covered sterile and non-sterile drug products, APIs and more06.06.18
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cGMP Manufacture | Clinical Trial Materials | Fill/Finish | Industry News
Dalton, Oryn Therapeutics in Development, Mfg. Pact
To provide cGMP aseptic liquid filling of Oryn’s RA drug in glass vials for Phase I trials03.15.18
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cGMP Manufacture | Clinical Trial Materials | Industry News
Dalton, Arch Biopartners Ink Drug Development and Mfg. Pact
To provide GMP prep and filling of AB569 into glass vials to support the Phase I trials05.08.17
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Breaking News | cGMP Manufacture | Clinical Trial Materials | Fill/Finish | Industry News
Dalton to Start GMP Mfg. for Inhalation Drug Candidate
Arch Biopartners expects AB569 to enter phase I later this year05.05.17
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Analytical Services | cGMP Manufacture | Drug Development | Formulation Development | Industry News | Methods Development
Dalton, Cerium Ink Development & Mfg. Agreement
Will provide formulation development, liquid filling, analytical method validation, QC testing and ICH stability services01.17.17
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cGMP Manufacture | Drug Development | Fill/Finish | Industry News | Methods Development
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APIs | Breaking News | Facilities | Fill/Finish | Industry News | Injectables | Lyophilization | Parenterals
Dalton Expands Sterile Filling and API Manufacturing Capabilities
Invests $5 million at Toronto facility08.30.16
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APIs | Breaking News | Chemistry | Drug Development | Facilities | Industry News | Process Development
Dalton Expands Services Portfolio
Adds flow chemistry reactor technology to service offerings07.13.16
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Chemistry | Drug Development | Industry News | Methods Development | Process Development
Dalton Adds Flow Chemistry Reactor Technology
Expands capabilities in the area of custom synthesis and process development07.06.16
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Analytical Services | APIs | Breaking News | Chemistry | Collaborations & Alliances | CRO News | Drug Development | Industry News | Validation
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Analytical Services | Breaking News | Drug Development | Industry News | Laboratory Testing | R&D | Toxicology
Dalton Forms Pact With Ramsey Lake Pharma
Will support toxicology studies for VR23 cancer treatment07.09.15
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Analytical Services | Bioanalytical Services | Bioassay Development | Breaking News | Capsules | cGMP Manufacture | Clinical Trial Materials | Clinical Trials | Collaborations & Alliances | Drug Development | Extractables and Leachables | Facilities | Fill/Finish | Formulation Development | GMPs/GCPs | Laboratory Testing | Lyophilization | Methods Development | Process Development | Solid Dosage/Semi-solids | Toxicology
Dalton Pharma Forms Manufacturing Agreement with Andes Biotechnologies
Will supply large molecule sterile dose manufacturing services for their Phase I/II clinical trials06.10.15
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Breaking News | Capsules | Extractables and Leachables | Facilities | Fill/Finish | GMPs/GCPs | Industry News | Lyophilization | Process Development | Vials
Dalton Expands Sterile Powder Mfg. Capabilities
Adds automated filling lines for small to large commercial batches01.28.15
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Bioassay Development | Breaking News | Chemistry | Collaborations & Alliances | Drug Development | Drug Discovery | Methods Development | Process Development | Toxicology
Cyclica, Dalton In Drug Development Pact
Dalton to synthesize and manufacture selected drug candidates04.11.13
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Breaking News | Capsules | Drug Development | Extractables and Leachables | Facilities | Fill/Finish | GMPs/GCPs | Industry News | Lyophilization | Process Development
Dalton Initiates Sterile Filling Expansion
To provide fully integrated sterile manufacturing services01.30.13
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Bio News | Bioassay Development | Biologics, Proteins, Vaccines | Breaking News | Drug Development | Methods Development | Process Development | Toxicology
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Biologics, Proteins, Vaccines | Breaking News | Collaborations & Alliances
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Breaking News | Drug Development | Industry News | Process Development
Dalton Helps Duke-NUS Achieve Clinical Milestone
Completes API development and manufacture for Phase I trial07.26.12
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Breaking News | Capsules | Chemistry | Extractables and Leachables | Facilities | Fill/Finish | Formulation Development | GMPs/GCPs | Lyophilization | Process Development | Promotions & Moves
Dalton Pharma Names Sales & Marketing Director
McCarthy responsible for global business development and marketing07.05.12
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Breaking News | Capsules | Chemistry | Drug Development | Extractables and Leachables | Facilities | Fill/Finish | GMPs/GCPs | Industry News | Lyophilization | Process Development
Dalton in Manufacturing Pact with Clarity
Will provide cGMP manufacturing, scale up, aseptic fill/finish services06.15.12
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Breaking News | Chemistry | Industry News
Dalton Pharma Gains GLP Certification
SCC certificate issued following inspection and audits05.30.12
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Analytical Services | Breaking News | Fill/Finish | Industry News
Dalton, Zafgen Enter Manufacturing Pact
Dalton Pharma Services has entered into a manufacturing services agreement with Zafgen, Inc. to provide cGMP aseptic fill/finish services and analytical support for Zafgen’s lead obesity treatment.05.17.11
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Breaking News | Drug Development | Industry News | Inspections
Dalton Pharma Successfully Completes Inspection
Dalton Pharma Services has successfully completed its Health Canada audit and has received a 'compliant' rating for its GMP manufacturing facility.02.02.10
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Breaking News | Clinical Trials | Collaborations & Alliances
