Get Full access to Know-How and Technology of manufacturing of +1000 molecules like Administrative Information, Technical Document Summaries, Quality, Clinical and Non Clinical Reports for your next drug development project
Each Know How
$5,000
Technical Consultation
$250 Annually
BP+ is a yearly paid subscription program from Burrard Pharma that gives users access to additional services otherwise unavailable or available at extra charge to regular clients. Services include consolation one by one with our formulation expert up to one hour with no charge.
What's inside a document?
Organized, Science prepared formulation with our detailed instructions so you never miss a step.
Administrative Information and Prescribing Information
Non Clinical Study Reports
Study Reports
Pharmacology
Primary Pharmacodynamics
Secondary Pharmcodynamics
Safety Pharmacology
Pharmacodynamic Drug Interactions
Pharmacokinetics
Method of Analysis
Absorption
Distribution
Metabolism
Excretion
Pharmacokinetic Drug Interactions
(nonclinical)
Other Pharmacokinetic Studies
Toxicology
Single-Dose Toxicity
Repeat-Dose Toxicity
Genotoxicity
Carcinogenicity
Reproductive and Development Toxicity
Local Tolerance
Other Toxicity Studies
Clinical Study Reports
Clinical Study Reports
Biopharmaceutics Reports
Bioavailability Study Reports
Bioequivalence Study Reports
In-vivo/In-vitro Correlation Studies
Analytical Method Used in Bioavailability
Study
Studies Pertinent to Pharmacokinetics using Human
Biomaterials
Human Pharmacokinetics
Human Pharmacodynamics
Clinical Efficacy and Safety Studies
Know how
Batch Formula
Description of manufacturing process and process control
Flow Diagram representing the steps of process
Manufacturing Flow Chart
Equipment Used in manufacturing process
Manufacturing Process
In Process Quality Control
Manufacturing process controls of critical steps and intermediates
In-Process Control Parameters during processing,
In-Process Control Parameters during Filling:
In-Process Control during Inspection:
In-Process Control during Packing:
Process validation and Evaluation
Quality Control
Process Validation and/or Evaluation
Validation of Analytical Procedures
Pharmaceutical Development
Post-approval Stability Protocol and Stability Commitment
Technology Transfer
Drug Substance
General Information
Nomenclature
Structure
General Properties
Characterisation
Elucidation of Structure and other Characteristics
Impurities
Control of Drug Substance
Specification
Analytical Procedures
Batch Analyses
Justification of Specification
Reference Standards or Materials
Container Closure System
Stability
Stability Summary and Conclusions
Stability Data
Drug Product
Description and Composition of the Drug Product
Control of Excipients
Analytical Procedures
Excipients of Human or Animal Origin
Novel Excipients
