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Webinars on Demand

Discovery & Development Formulation

The side-effects of bad data in API development and manufacture

| Sponsored by Malvern Panalytical

Innovation is key to delivering new drugs faster and cheaper, while tailoring them to patient needs.

Manufacture Vaccines

Unleashing the Power of Cyclodextrins in Vaccines

| Sponsored by Roquette

During this webinar, Roquette will explore innovations within vaccine formulations.

Manufacture Advanced Medicine

Fiber-based chromatography to improve productivity in downstream AAV processing

| Sponsored by Cytiva

As more AAV-based gene therapies move towards the clinic, there is a growing need for scalable and cost-effective production processes that maintain virus quality.

Manufacture Advanced Medicine

Efficient production process for adeno-associated viral vectors

| Sponsored by Cytiva

The use of adenovirus-associated virus (AAV) vectors in gene therapy is growing.

Manufacture Quality & Compliance

The challenges and key components of conducting investigations in Microbiology

| Sponsored by Cambrex

Out of trend (OOT) and out of specification (OOS) results for Microbiology testing are inevitable challenges that every sterile manufacturing environment must face.

Manufacture Quality & Compliance

AMLM: the perks of method performance verification in pharmaceutical quality framework

| Sponsored by Hovione

Analytical Method Lifecycle Management (AMLM) principles require a holistic perspective where method robustness is considered together with process and product variability.

Manufacture Advanced Medicine

Advanced logistics for advanced therapies: Evidence using VIA Capsule™ cryogenic system

| Sponsored by Cytiva

Cell therapy logistics is challenged by complex processes, inefficiency, and lack of flexibility to accommodate manufacturing, clinic, and patient needs

Manufacture Bioprocessing - Upstream & Downstream

Simplicity and robust control with the Erbi Breez ™ True Perfusion™ microfluidic bioreactor system

| Sponsored by Erbi Biosystems

Upstream process intensification efforts are becoming mainstream in every biopharma R&D lab and clinical program.

Manufacture Standards & Regulation

Practical Management of Pharmaceutical Impurities

| Sponsored by Hovione

With this webinar we pretend to look at the different sorts of impurities that may occur in pharmaceutical products and discuss current regulations, requirements and control strategies to be followed in order to comply with the current demands.

Discovery & Development COVID-19

Post-Pandemic Planning: What Will Change in the Clinical Supply Chain?

| Sponsored by Thermo Fisher Scientific

Join Thermo Fisher Scientific’s drug development and clinical services experts for another Q&A session to hear about the company’s innovation.

Discovery & Development COVID-19

Post-Pandemic Planning: What Will Change in Early-Phase Drug Development?

| Sponsored by Thermo Fisher Scientific

Join Thermo Fisher Scientific’s drug development and manufacturing experts for a unique, extended Q&A session and learn how to start navigating the new normal.

Business & Regulation Advanced Medicine

FDA Accelerated Approval Pathways for Cell and Gene Therapy products

| Sponsored by Thermo Fisher Scientific

The cell and gene therapy regulatory landscape is rapidly evolving. Join this webinar to discover the approaches available to this industry to accelerate the approval of cell and gene therapy products.

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