The growing interest in alternative routes of drug and vaccine administration has experts predicting that the market for microneedle drug delivery systems could exceed $30 billion by 2025. The industry is on the threshold of bringing into commercial production a new generation of transformative skin-mediated delivery systems. That is why you cannot afford to miss this two-day intensive conference. Pharma Ed's Microneedle & Transdermal Drug Delivery Forum 2022 brings together leading researchers in the field to share the most recent advances in the design, formulation, and delivery of skin-mediated therapies and vaccine

This two-day conference will examine the safety, quality, and regulatory issues involved in a wide array of contexts central to the pharmaceutical and biotech industries, including drug packaging and delivery components, single-use systems, medical devices, and parenteral drug products. We will focus closely on the keys to satisfying recent revisions to several applicable USP chapters, FDA guidances & other international regulatory requirements for best practices in materials and chemistry characterization for drugs, biologics, delivery systems, and primary & secondary packaging.

Regulators in North America and Europe are requiring stricter standards for the manufacture and safety testing for combination products in both the Pharma and med device industries. This two-day summit features expert insight into CP product development, and the complex quality, safety, and regulatory compliance issues facing the CP market. Pharma Ed’s Combination Products Summit 2022 provides comprehensive coverage of current and future trends in combination product development for drugs, biologics and medical devices.

As the Cannabis market continues to evolve, the state of scientific knowledge on medicinal Cannabis remains immature, and the regulatory environment in North America fragmented and contested. That is why you cannot afford to miss Pharma Ed’s Canna Pharma. This two-day scientific conference explicitly links current knowledge and practice in the pharmaceutical and Cannabis industries, providing a forum for scientific dialogue and collaboration aimed at advancing best practices and enlarging the scope of therapeutic applications in this growing market. Pre-clinical and clinical research scientists, product developers, cannabis cultivators, processors, & testing labs, and public policy makers will come together to advance Cannabis science.

Regulators in North America and Europe are requiring stricter standards for environmental monitoring systems, facility cleaning and disinfectant qualification, aseptic cleanroom operations, filtration, sterilization, and aseptic process simulation (or media fill). This two-day summit features expert insight into the robust aseptic processing requirements facing the industry. Pharma Ed’s Aseptic Processing Summit features comprehensive coverage on the implementation and management of the latest knowledge in aseptic, barrier, containment, and aseptic best practice technologies.

Can you implement the best science-, risk-, and statistics-based approaches to cleaning validation? Today’s regulators are now expecting ADE monographs and comprehensive risk assessments of your organization’s cleaning validation protocols. Pharma Ed’s Cleaning Validation Summit brings together leading industry experts to illuminate best practices and help you meet regulatory requirements.