Pharmaceutical Manufacturing Primer covers essential aspects of small molecule drug production. It begins with the unique ingredients incorporated into these medications, emphasizing the roles of active pharmaceutical ingredients (API) and excipients. Various chemical synthesis methods are demonstrated, including organic, linear, convergent, and stereoselective approaches. The intricate purification process and stringent regulatory aspects of API production are explained, along with supplier validation requirements. This foundational class continues with formulation goals and dosage form characteristics, such as tablets and capsules. It ends with a deep dive into packaging considerations, highlighting fill and finish methodology, regulations, tamper resistance measures, anti-counterfeit technologies, and supply chain management, including cold chain logistics. Grab your spot today for this comprehensive class that provides insight into the intricate manufacturing processes of small molecule drugs!

OSHA Bloodborne Pathogen Standard Primer focuses on preventing the spread of infectious diseases by managing the chain of infection and handling biohazardous materials safely. This class sets guidelines for employers and employees on safe practices when dealing with potentially infectious materials. The standard covers biosafety levels, personal protective equipment, waste management, and disinfection procedures. Additionally, this primer explains the OSHA Emergency Response Procedures, including spill protocols, emergency response plans, and incident follow-up, which are crucial for worker safety. Compliance documents such as a biosafety manual and exposure control plan are also reviewed. Register today and become compliant with the OSHA Bloodborne Pathogen Standard!

Small Molecule Drug Discovery Primer 201 builds upon the foundational knowledge from Small Molecule Drug Discovery Primer 101. This class takes a deep dive into early screening techniques, including discovery platforms, high-throughput screening, and novel target identification. It breaks down the strategies used for lead optimization, along with drug design methodology and approaches. Uncover the crucial criteria for transitioning from discovery to development, including how to rigorously evaluate data from in silico, in vitro, and in vivo assets. Join Small Molecule Drug Discovery Primer 201 and continue to increase your pharmaceutical research knowledge!

Medical Device Development Primer broadly explores the five pivotal stages of medical device development. This class focuses on the workflow at each step, from evaluating market opportunities and rigorously assessing concepts to crafting engineering designs and scaling manufacturing. This primer unlocks the secrets of FDA guidance's pertaining to process design, qualification, and monitoring. It ends with a look at product risk assessment and reimbursement, summarizing their role in management's momentous go/no-go decisions. Enroll today to embark on this exciting quest toward groundbreaking medical device development!

Medical Device Commercialization Primer navigates the intricacies of the approval pathways, the excitement of a launch, and the rigors of post-market surveillance. This class reveals best practices for business preparations, sales, marketing, and reimbursement—ensuring corporate-wide readiness and effective healthcare promotion. It wraps up by highlighting the sponsor’s responsibility for monitoring device performance to ensure ongoing patient safety and FDA compliance. Join us for the fast-paced Medical Device Commercialization Primer and equip yourself with the tools and knowledge to create a successful commercialization plan for your medical device. Register now