- Essentials of EU and US Regulatory Affairs for Human Medicinal Products
- Acute Coronary Syndromes: Non ST Elevation MI
- How to Obtain Approval to Conduct Clinical Trials in the EU
- Orphan Drug Applications in the EU and USA
- An Introduction to Good Manufacturing Practice (GMP) for Drug Products
- Atrial Fibrillation 1: Pharmocologic Approach
- Goals & Objectives
- Team Communication
- Conflict Resolution
- Meeting Management
- Interviewing/Selection
- Complaint Handling
- Problem Solving
- Delegation Skills
- Negotiating Skills
- Diversity & Cultural Awareness
- Managing Poor Performance
- Corporate Ethics
- Sales Effectiveness
- Presentation Skills
- Creativity & Innovation
- Customer Service
- Risk Management
- Change Management
- Coaching
- Team Building
- Leadership
- Acute Coronary Syndromes: ST Elevation MI
- Atrial Fibrillation 2:Non-pharmocologic Approach
- The European Centralised Procedure (CP)
- The Mutual Recognition Procedure (MRP)
- Preparing Submissions in the Common Technical Document (CTD) Format
- Electronic Common Technical Document (eCTD)
- Variations to Marketing Authorisations in Europe
- Registration of Monoclonal Antibodies
- The ANDA: Requirements for Obtaining FDA Approval for a Generic Product in the USA
- The NDA Process: Requirements for Obtaining Approval for a New Drug in the USA
- The Decentralised Procedure (DCP)
- An Introduction to Drug Safety and Pharmacovigilance
- Pharmacokinetics and Pharmacodynamics in Drug Registration
- An Introduction to ICH Good Clinical Practice (ICH-GCP)
- An Introduction to Clinical Trial Preparation and Design
- An Introduction to Clinical Trials in India
- Clinical Trial Monitoring: Site Evaluation and Set-up
- Introduction to Clinical Trials and Drug Development
- Clinical Trial Monitoring: Study Monitoring, Documentation and Closure
- Preparing for a GCP Audit or Inspection.
- The IND: How to Gain Approval for Clinical Trials in the USA
- Introduction to Retail
- J0 e-workbooks
Products
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| Items 1 to 50 of 74 total |
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