Biotechnology And Pharmaceutical Development Courses

Single-Use Technology in Biopharma Manufacturing Training Course offers professionals in the pharmaceutical and biotechnology industries an in-depth understanding of the practical application, benefits, and challenges associated with SUT

WHO Prequalification of Medicines and Vaccines Training Course provides pharmaceutical and public health professionals with the critical, trending regulatory knowledge required to successfully navigate the complex submission and inspection landscape for the 2024-2025 cycle and beyond

Stability Testing and Shelf-Life Determination Training Course is designed to provide participants with a deep understanding of the techniques, methodologies, and regulations involved.

Regulatory Strategy for Companion Diagnostics Training Course is designed to equip professionals with the knowledge and strategic acumen needed to navigate this complex landscape, from initial biomarker discovery and co-development to market access and post-market surveillance.

Regulatory Submissions- IND, NDA, BLA, MAA Documentation Training Course is designed to equip professionals with the critical knowledge and practical skills needed to navigate the complex landscape of regulatory documentation for Investigational New Drug (IND), New Drug Application (NDA), Biologics License Application (BLA), and Marketing Authorization Application (MAA) submissions.

Regulatory Strategy for Combination Products Training Course is designed to provide professionals with a comprehensive understanding of the complex regulatory framework surrounding combination products

Risk-Based Monitoring (RBM) in Clinical Trials Training Course is designed to equip clinical research professionals with the essential knowledge and skills required to implement RBM strategies effectively.

Root Cause Analysis (RCA) and CAPA for GMP Deviations Training Course equips professionals with the knowledge and tools needed to investigate GMP deviations effectively, identify root causes, and implement corrective and preventive measures.

Strategic Portfolio Management in Drug Development Training Course is designed to empower leaders and professionals in the biopharmaceutical sector with the advanced skills needed to navigate the complex and high-stakes world of drug development

Sterile Product Manufacturing and Aseptic Processing Training Course is designed to equip professionals with the essential skills to manage aseptic processes and comply with strict industry standards to avoid contamination and ensure the integrity of sterile drugs.

Regulatory Affairs Strategy for the EMA (EU) Training Course is a designed for professionals in the pharmaceutical, biotechnology, and medical device sectors.

Single-Cell Genomics Data Processing Training Course is designed to empower researchers, clinicians, and data scientists with the foundational and advanced skills necessary to navigate the single-cell genomics data landscape.