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Dalton Pharma Services

Headquarters

Canada

Products & Services

Accelerated Stability Testing

Antibody Drug Conjugate (ADC)

API Purification and Process Development

Artesunate

Bioburden Analysis

cGMP Sterile API Manufacturing

Clinical Sterile Vial Manufacturing

Commercial Product Stability Testing

Comparator Stability Testing

Complex Active Pharmaceutical Ingredients

Continuous Process

Controlled Drug Products Stability Testing

Custom Peptide Synthesis

Custom Synthesis of Pharmaceutical Impurities

Development of ADC formulations

Dev. & Evaluation of Stability Indicating Methods

Fine Chemical

Forced Degradation Studies

Formulation Evaluation Stability Testing

GMP Friendly Alternative Synthetic Routes Development

ICP-MS Elemental Analysis

Impurity Reference Standards

Impurity Screening

Intermediate Stability Testing

IP Protected Synthetic Routes Development

Isolation of Active Pharmaceutical Ingredients

Long-Term Stability Testing

Lyophilization

MG to Multi-kilogram Scale Batch (up to 300L Reactors)

Microbiology

Microscopic Procedures

Optimization of Existing Synthetic Routes

Particulate Matter Testing

Pharmaceutical Intermediates

Photostability

Polymorphic Screening

Polymorphism Study

Process Parameterization & Optimization

Reference Standard Materials

SEC-MALS

Sterile Liquid Injectables

Sterile Lyophilized Vials

Sterile Powder Filling in Vials

Sterility Testing

Structure Elucidation of Impurities

Water Testing