Pharmaceutical Training
Keep your organization up-to-date on what is happening in the Pharmaceutical Industry.
Your Company’s Professional Development is critical for its continued success. The professional development of your staff can be the difference between understanding and meeting cGMP regulations, successful regulatory submissions, and regulatory rejection letters and violations.
Our Pharmaceutical Training Programs are designed to give your team the interactive, hands-on learning needed to maintain a competitive advantage and ensure regulatory compliance.
Our webinars and training courses present information and contain exercises that use current situations and problems common to the pharmaceutical industry to help your staff understanding the pharmaceutical paradigm. Our subject matter experts bring their extensive knowledge and experience to the coursework.
Some recent examples of webinars and training courses are:
- Nitrosamines in Pharmaceuticals
Nitrosamines are considered genotoxic impurities. This 1-hour webinar discusses the current Health Authority Guidance and expectations in dealing with these potential impurities in your drug substance, drug product and packaging components.
- Quality Agreements – What are they? Why do I need them?
This 1-hour presentation discusses the preparation, contents and implementation of Quality Agreements as part of your interactions with contract development and manufacturing organizations (CDMOs) that your firm may be working with for the develop, prepare, and test your preclinical, clinical, and commercial drug substances and drug products.
- Artificial Intelligence in Pharmaceutical Drug Development
A current ‘hot topic’. This short course explains the basic concepts of Artificial Intelligence, and how it has been and can be used the drug development and manufacturing paradigm to potentially reduce development timelines and costs.
- Health Authority Inspections
This 1-hour webinar discusses what may happen and possible outcomes when FDA inspectors knock on your manufacturing facility’s front door and announce their intent to conduct a site inspection. Included are suggestions for how your team members should conduct themselves during the inspection and how to respond to FDA comments and inspection finding.
- Quality-by-Design in Drug Development
This short course which discusses the application of Quality-by-Design (QbD) and Design Space concepts to the development of drug substances and drug products. The program discusses what QbD and Design Space are and are not and, how Regulatory Authorities may view submissions which are made containing these concepts.
- Technology Transfer: What Does It Involve? Why Do I Need It?
This webinar provides insight into the importance of knowledge and technology management and transfer throughout the pharmaceutical development lifecycle It discusses how the current thinking around the use of artificial intelligence and machine learning may impact and possibly enhance drug product quality.
Participation can be virtual or in-person on-site.
We can develop, customize programs on a variety of pharmaceutical related topics that may be of interest your organization.
Our programs can be tailored to any schedule or location to meet your specific organizational requirements.
Contact Us for a Quote.
RhoTau Pharma Services’ goal is to assist our clients, be they consumer product, generic or innovator firms, small start-ups or large, global pharmaceutical or biotechnology companies, with strategic and tactical implementation designed to rapidly bring their small or large molecule products to peak sales in order to fully realize their life cycle potential.
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Operations Support
Regulatory, Quality Assurance & CMC
