Most regulated organizations conduct internal audits regularly, yet many are still surprised by inspection findings.

Charles H. Paul

• March 27, 2026
• 60 Minutes
• US$149.00
• Enroll

Human error is often blamed after equipment failures, but rarely is it systematically eliminated. Organizations tend to respond with more training, reminders, or disciplinary actions-yet the same failures repeat. Why? Because most inspection systems depend on memory, experience, and individual judgment rather than engineered reliability.

Charles H. Paul

• April 3, 2026
• 60 Minutes
• US$149.00
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Managing performance in life science working environments requires a unique blend of leadership skill, regulatory understanding, and organizational awareness. Unlike traditional industries, pharmaceutical, biotech, and medical device companies operate under intense scrutiny, complex documentation requirements, and strict quality system expectations.

Charles H. Paul

• April 6, 2026
• 60 Minutes
• US$149.00
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Managing cross-functional project teams in the life sciences requires a sophisticated blend of leadership, regulatory knowledge, interpersonal skill, and project structure. Drug development, clinical trials, manufacturing scale-up, and medical device commercialization all rely on contributions from various specialized functions-such as Quality, Regulatory, Clinical, Manufacturing, Supply Chain, R&D, and Technical Operations. Because each discipline brings its own priorities, vocabulary, timelines, and compliance obligations, effective cross-functional leadership becomes essential for ensuring aligned progress, consistent documentation, and timely regulatory milestones.

Charles H. Paul

• April 8, 2026
• 60 Minutes
• US$149.00
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Drug development is inherently uncertain, spanning complex scientific processes, multi-phase clinical studies, regulatory review cycles, and interdependent CMC activities. Risk-based project planning provides a proactive, structured approach for anticipating challenges, evaluating their potential impact, and making informed decisions that protect timelines, budgets, and compliance obligations. This webinar introduces participants to the principles, tools, and practical applications of risk-based planning as required by modern regulatory expectations and global standards such as ICH Q9 and ICH Q10.

Charles H. Paul

• April 10, 2026
• 60 Minutes
• US$149.00
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Streamlined SOPs and Work Instructions are essential for enabling efficient development, reliable execution, and consistent compliance in life science organizations. Yet many companies struggle with bloated, unclear, or overly complex documents that slow productivity, increase training requirements, and contribute to human error. This webinar provides a practical, structured approach to designing, writing, and maintaining SOPs and WIs that support maximum operational efficiency and utilization effectiveness.

Charles H. Paul

• April 17, 2026
• 60 Minutes
• US$149.00
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Agile project management is widely recognized for its ability to accelerate delivery, improve cross-functional visibility, and promote rapid problem solving-capabilities that have become increasingly valuable in the highly regulated GMP and GCP environments of the life-sciences industry. This webinar provides a practical, compliance-centered exploration of how Agile principles can be successfully applied to pharmaceutical, biotech, medical device, and clinical research projects without compromising regulatory expectations or documentation rigor. Participants learn how Agile can be adapted to meet the stringent requirements of FDA, EMA, and global regulatory frameworks while still offering the flexibility and speed that teams need to navigate modern development and quality challenges.

Charles H. Paul

• April 22, 2026
• 60 Minutes
• US$149.00
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Global product launches for medical devices and pharmaceutical products are among the most complex undertakings within the life sciences industry. Launch success depends on precise coordination of regulatory strategies, technical documentation readiness, manufacturing scale-up, supply chain reliability, marketing alignment, and post-market surveillance capabilities. This webinar provides a comprehensive, highly structured overview of how to plan, implement, and sustain global product launches that meet regulatory requirements while achieving commercial objectives in multiple international markets.

Charles H. Paul

• April 27, 2026
• 60 Minutes
• US$149.00
• Enroll