Drug Development Training: Keeping Your R&D Operations Compliant
At CfPIE, we understand the necessity for compliance training programs that fit with your team’s schedule and individual needs. Our Drug Development Process from Concept to Market course allows your company to ensure that those directly involved in drug development, like R&D scientists, are communicating effectively with teams in statistical analysis, sales, marketing and the like, to share information and develop a common understanding of the product lifecycle.
The course deals directly with the full scope of the drug and biologics development process, touching on topics ranging from creating a regulatory framework, working within FDA parameters, and project management of cross functional teams.
In particular, your research and development procedures are dependent upon having a trained and knowledgeable staff that can anticipate problems in the process and work together to develop solutions and clear roadblocks. Adhering to regulatory guidelines is not something that can be checked off at the beginning of a drug development timeline. It must be practiced every day by every team member in order to keep your lab FDA-compliant, and in order to produce reliable, replicable results and bring your drugs/biologics to market.
Our instructors have real-world training, and can help your teams tackle the issues you are facing now. Our course is even adaptable and customizable for your specific company needs. We are also happy to offer a short-form course for new professionals and administrative/support staff.
To learn more about the course and book your training session, visit the Drug Development Process from Concept to Market course page. Further information and a detailed schedule is available in our course brochure.
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