Biopharmaceutical Courses

CfPA offers numerous courses in the field of Biopharmaceutical/Biotechnology:

• Advanced Validation and Commissioning for Pharmaceutical, Biopharmaceutical and Device Manufacturing
• Assay Development and Validation for Biopharmaceuticals
• Auditing and Inspecting Clinical Research in the Global Environment
• Auditing and Inspecting Preclinical Research for GLP Compliance
• Biosafety of Biological Drug Products
• Biostatistics for Non-Statisticians
• Case Report Forms and Other Instruments for Clinical Data Collection
• cGMP and Quality Issues for Biopharmaceuticals
• Characterization of Proteins: Isolation and Analysis
• Clinical Data Management in Pharmaceutical Research and Development
• Design, Engineering and Validation of Biopharmaceutical Process Systems
• Developability Assessment
• Developmental and Reproductive Toxicology
• Downstream Processing in Biotechnology
• Drug Delivery Technology
• FDA Requirements for Registration of Biopharmaceuticals
• Fundamentals of Biochemistry: Background for Biotechnology
• Fundamentals of Gel Electrophoresis
• Fundamentals of Molecular Biology and Genetic Engineering
• Good Clinical Practices (GCP)
• Good Laboratory Practices (GLP)
• Good Tissue Practices (GTP)
• ICH-Q7A
• LAL Testing: Drugs, Medical Devices and Biopharmaceuticals
• Lyophilization Technology
• Microbiological Control and Validation
• Monitoring of Clinical Drug Studies
• Non-Clinical Safety Evaluation and Drug Development
• Outsourcing Clinical Development
• Peptide and Protein Drug Delivery
• Pharmaceutical Technology Transfer
• Principles of Contemporary Immunology
• Process Analytical Technology (PAT)
• Root Cause Investigation for CAPA
• Stabilization of Protein Drugs, Biologics and Devices
• Writing and Implementing Clinical Protocols in the Global Process of New Drug Development

For More Information on these Courses Click here