Our team of biopharmaceutical professionals work diligently to gain the thorough understanding of different compounds, to help you effectively develop quality drug formulation and development.
Our core services include process development, formulation development, preclinical (toxicology) and batch production.
1. Master formulation you need to produce a a drug either in clinical size or commercial in one place.
2.You will have full access to our knowledge, manufacturing secrets, formulation, master formula, products specifications, studies and more from a single dashboard.
So successful in fact, that our customers have made over $500 million dollars on the platform to date! Master formulation you need to produce a a drug either in clinical size or commercial in one place. You will have full access to our knowledge, manufacturing secrets, formulation, master formula, products specifications, studies and more from a single dashboard.
Basic information on the chemical
Mechanism of action
Pharmacology class
Pharmacology
Pharmacokinetics
Toxicology
Overview of biopharmaceutics
Clinical pharmacology
Efficacy and safety
Benefits and risks
Nomenclature
Structure
Physicochemical properties
Batch formula
Description of manufacture process and controls
Controls of critical steps and intermediates
Product testing, validation and evaluation
Manufacture process development
Determine impurities
Components of drug product
Microbiological attributes
Compatibility
Specification of drug substance
Analytical procedures
Batch analyses
Burrard Pharma comprehensive drug development services are designed to reduce your costs and time required, helping you achieve your drug discovery goals. Our creative scientists have accumulated decades of industry-specific experience. This enables our firm to create molecules to the specifications you need efficiently. As well, our drug development experts will optimize your processes and scale up the operations by your requirements for drug manufacturing.
Our team of biopharmaceutical professionals work diligently to gain the thorough understanding of different compounds, to help you effectively develop quality drug formulation and development.
Our core services include process development, formulation development, preclinical (toxicology) and batch productions.
Stability studies
Lyophilization – Cytotoxic formulation
Terminal sterilisation
Potent Formulation
Highly potent product formulation
Peptides/Proteins/Enzyme
Monoclonal antibodies (MAB)
Nanoparticles
Inactivated & attenuated live vaccines
Dry Powder
Filling of both liquid and dry powder
Sterile crystallization
Formulation of disperse systems
Filling and lyophilisation of colloidal drug carriers, such as liposomes, nanoparticles, microemulsions and micelles
Technology portfolios such as homogenization, diafiltration, organic solvent distillation, liposome loading and sterile filtration
With over a decade of international experience, Burrard Pharmaceuticals is well positioned to navigate through any complex drug manufacturing projects.
We are experts in producing traditionally complex products such as cytotoxic’s, highly potent compounds, biologics, lyophilized products and Antibody-Drug Conjugates. Often, parenteral manufacturing is a very complicated process, and we are here to help you simplify it and ensure the excellence in development.
Vial filling- Aseptic
Solid-Semi Solid- Liquid
Packaging – Emulsion – Sterile
Stability storage
Lyophilization – Cytotoxic
Terminal sterilisation
Potent Formulation
cGMP production of complex compounds
Highly potent products
Cytotoxics
Peptides/Proteins/Enzyme
Monoclonal antibodies (MAB)
Nano particles
Inactivated & attenuated live vaccines
Dry Powder
Filling of both liquid and dry powder
Clinical and commercial lyophilized products
Sterile crystallization
Formulation of disperse systems as well as filling and lyophilisation of colloidal drug carriers, such as liposomes, nanoparticles, microemulsions and micelles
Technology portfolio such as homogenization, diafiltration, organic solvent distillation, liposome loading and sterile filtration
Technology transfer
Stability storage
Lyophilization cycle development
Analytics
Engineering
Microbiological services
Packaging and kitting
Regulatory submission and support
Small molecules
Biologics
Liposomal systems
Antibody-drug conjugates
Non-destructive testing and weight checking
Dual filling
Cold chain filling
Process design with high yield optimization
Biomolecule formulation
Process design and development
Solutions, suspensions as well as development of lyophilized forms
Sizes: 2mL to 10mL
All primary packaging options such as stoppers, vials, and seals
Multiple filling
Leading technology in lyophilization with automated loading/unloading system
Meet FDA, EU and JP regulatory standards
Cytotoxic’s
Highly potent molecules
Small molecules
Biologics
Antibody-drug conjugates
Pandemic vaccines
Conjugates
Adjuvants
Preventive vaccines
Seasonal vaccines
Transfer scientific findings from one organization to another often take the research further to develop something new or better. Successful product innovations have often begun through the usage of technology transfer.
Large Volume Parenterals (LVP)
Small Volume Parenterals (SVP)
Pre-filled Syringes
IV products
Blood bags
Dialysis concentrate solutions and powders
Plasma Fractionation
Biotechnological Plants
Multipurpose Pharmaceutical Plants
PVC and PP bags
Plastic and glass bottles
Bottles with Blow Fill Seal technology (BFS)
Bottle with Stretch Blow Molding Technology (SBM)
Water
Sodium Chloride
Glucose
Dextrose
Mannitol
Amino acids
Plasma expanders
Heparin
Ciprofloxacin
Metronidazole
Paracetamol
Canisters
Bags
Cartridges
Diacetate bags
Priming bags
Multi-chamber bags
Continuous Ambulatory Peritoneal Dialysis bags
Bicarbonate cartridges
Single Bags
Double Bags
Triple Bags
Tetra Bags
Interferon
Erythropoietin
Epidermal Growth Factor
Insulin
Human Growth Hormone
Monoclonal Antibodies
Antibiotics
Solution & Suspension Small Volume Parenteral
Lyophilized Small Volume Parenteral
Non-Sterile Liquids or Suspensions
Terminal Sterilization