Sitemap > Events > Oncology
- What is Nanotechnology? An Online Training Course
- Analytical Methods Validation for FDA Compliance
- Managing Risk in Pharmaceutical Manufacturing
- Laboratory Control Systems
- cGMP Auditing - Strategies for Compliance
- INDs, NDAs vs CTDs Global Regulations
- Microencapsulation and Particle Coating
- Non-Clinical Drug Safety Evaluation and Drug Development
- Pharmaceutical cGMPs and FDA Inspections
- Preparing for and Surviving an FDA Inspection
- Calibration in the FDA Regulated Industry
- Laboratory Analysis in Clinical Trials
- Fundamentals of Biochemistry: Background for Biotechnology
- Fundamentals of Molecular Biology and Genetic Engineering
- ISO 13485, ISO 9001 and QSR Regulations for Medical Device Companies
- Good Laboratory Practices (GLP)
- Combination Product Development: Safety/Registration/Approval
- Point of Care Testing: Innovation on the Move
- Pharma Sales Force Effectives Conference 2007
- The GLP Study Director
- Computerized Systems Used in Clinical Investigations: the New FDA Guidance
- Early Stage Clinical Development
- Near Infra-Red Spectroscopy
- Applied cGMPs for Pharmaceutical and Allied Industries
- Refractories for Industrial Applications
- Biopharmaceutical Process Systems
- Drug Discovery and Development Summit
- Drug Product Stability and Shelf-Life
- Critical Process Cleaning and Cleaning Validation
- Annual Product Reviews (APRs) For Pharmaceuticals
- Microencapsulation and Particle Coating
- Documentation Management and Control
- ISO 13485, ISO 9001 and QSR Regulations for Medical Device Companies
- Monoclonal Antibodies 2008
- Biomarkers 2008: Discovery, Validation and Application of Biomarker Technology
- Lead-Finding Screening
- Personalised Medicine
- Compound Management & Integrity 2008
- Developing Commercial Oncology Therapies
- Clinical Trials Conference 2008
- Cancer Biomarkers Development and Clinical Use
- ICH Q10: Pharmaceutical Quality System
- ISO 13485, ISO 9001 and QSR Regulations for Medical Device Companies
- ICH Q9: Managing Risk in Pharmaceutical Manufacturing
- U.S. FDA Drug Development and Compliance
- Role of PAT and QbD in Biologic Drug Production
- Tablet Production for Operators and Supervisors
- Pharmaceutical Quality Assurance and Control
- Conducting Effective Quality Audits