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EVENTS

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SPOTLIGHT

ICH Q12, Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management, is a transformative document that will shape global regulatory submissions and practices. Adopted in November 2019, it has a wide scope of applicability across pharmaceutical drug substances and product

JAN 26, 2021
DRIVING PATIENT SAFETY, PRODUCTION EFFICIENCY AND QUALITY IN PARENTERAL MANUFACTURING THROUGH THE USE OF CONTAINER TRACEABILITY
Health authorities and regulators are increasingly looking for much higher levels traceability during the manufacture of parenteral medicines. The most common processes and technologies applied to achieve compliance are now reaching their technical limitations and as such new approaches are needed t...
FEB 17, 2021
CHALLENGES & SUCCESSES OF ICH Q12 RELATED SUBMISSIONS
ICH Q12, Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management, is a transformative document that will shape global regulatory submissions and practices. Adopted in November 2019, it has a wide scope of applicability across pharmaceutical drug substances and product...
FEB 23, 2021
GMP & OCCUPATIONAL EXPOSURE REQUIREMENTS TO MANUFACTURE HIGH POTENT STERILE PRODUCTS IN SHARED FACILITIES
Contamination and Cross Contamination Control in shared Facilities to protect the product, the operators, and the environment, especially working with highly potent/toxic sterile pharmaceutical substances. The session will cover the GMP and Occupational Safety Requirements for highly potent sterile ...
WEBINAR: PARTICLE ENGINEERING IN PHARMACEUTICAL SOLIDS PROCESSING
Webinar title: Particle Engineering in Pharmaceutical Solids Processing: Surface Energy Considerations Topic: This webinar presented by Dr Daryl Williams from Imperial College London reviews the surface energy and surface energy heterogeneity of crystalline solids, methods for the measurement of sur...
WEBINAR - THE 7 DEADLY SINS OF PHARMA JOB APPLICATIONS
For the last 10 years, here at GetReskilled, we have been helping people from a wide range of backgrounds make mid-career changes into well-paid jobs and careers into the pharmaceutical and medical device manufacturing industries. With a decade of experience in the industry we’ve come to learn what ...
DIGITAL BEST PRACTICES FOR ACCELERATING DRUG DEVELOPMENT
Watch this on-demand webinar to hear from Robert Albert, Collaboration Lead at AstraZeneca, and Ellen Reilly, VP of Life Sciences at DocuSign, on the digital future of pharmaceuticals and the best practices for investing and adopting eSignature solutions to reduce development cycle time and generate...
PRINCIPLES OF DIFFERENTIAL SCANNING CALORIMETRY (DSC) – THE MOST USED THERMAL ANALYSIS TECHNIQUE IN PHARMACEUTICALS
Differential scanning calorimetry (DSC) is the most frequently used thermal analysis technique alongside TGA, TMA and DMA. DSC is used to measure enthalpy changes due to changes in the physical and chemical properties of a material as a function of temperature or time. The method allows you to ident...
BIOPHARMA DEAL MAKING: LESSONS LEARNT FROM CASS BUSINESS SCHOOL’S STUDY OF STRATEGIC DEALS AND CORPORATE PORTFOLIO MANAGEMENT
Extensive prior studies have shown strong positive effects for targets and negative effects for acquirers but, they have focused on measuring value creation from individual deals, not a firm’s overall programs of activity and performance over longer time periods. This far reaching study analyzed ove...
PRACTICAL APPLICATION OF RMM IN PHARMACEUTICAL MANUFACTURING
The application of Rapid Microbiological Methods (RMM) is a topic that has gained interest over the past few years as pharmaceutical manufacturers investigate and look to gain improved efficiencies across all areas of their businesses – including the microbiology laboratory. This pharma webinar dem...
HOW TO IMPLEMENT NIR SPECTROSCOPY INTO THE PHARMACEUTICAL PROCESSES
This pharma webinar examines the technique of Near Infrared spectroscopy, and how it can be used in pharmaceutical research and development. Potential uses of this excellent PAT tool include identifying raw materials, process control testing and the examination of a final product. We also explore th...
NAVIGATING THE COMPLEXITIES OF PHARMACEUTICAL MANUFACTURING REGULATIONS
While regulatory enforcement agencies around the world have increased scrutiny on quality assurance/quality control programs, pharmaceutical manufacturers are increasingly looking for ways to lean out the manufacturing process without compromise to product quality. This push and pull conundrum has m...
THE TRUTH ABOUT PHARMACEUTICAL DRUGS AND THE MEDICAL INDUSTRY - PART 1
investigates how the influence of pharmaceutical money and guild interests has corrupted the behavior of the American Psychiatric Association and academic psychiatry during the past 35 years. He documents how the psychiatric establishment regularly misled the American public about what was known abo...
PRE-FILLED SYRINGES IN CLINICAL TRIALS
After decades of domination by small-molecule drugs, one could say that the pharmaceutical industry is increasingly thinking large. More than 60% of drugs currently in clinical development are biologics for parenteral administration.
PATIENT-CENTRIC PHARMACOVIGILANCE: BUILDING BETTER OUTCOMES THROUGH INTEGRATED TECHNOLOGY
Pharmacovigilance (PV) is the science and process of monitoring the safety of medicines, taking action to reduce the risks and increase the benefits of medicines to patients and maintaining regulatory compliance. As biopharmaceutical companies increasingly seek to achieve global patient access, ther...
SIGNAL DETECTION & TRENDING IN VETERINARY PHARMACOVIGILANCE
This webinar focuses on the process of signal detection and trending. Signal detection and trending is a powerful tool used in the management of veterinary medicines. The process of signal detection (Signal Generation, Signal Strengthening, Signal Assessment and Signal Follow-Up) can generate more s...