The Future of excipient audits and COVID-19. Iain Moore President EXCiPACT A brief explanation of the EXCiPACT Certification Scheme for pharmaceutical excipients will be followed by an explanation of how the Scheme has been adapted without compromising quality as a result of the COVID-19 pandemic. The use of remote audits within the Scheme will be... Read more » The Future of Excipient Audits & COVID-19.
The Future of excipient audits and COVID-19. Iain Moore President EXCiPACT A brief explanation of the EXCiPACT Certification Scheme for pharmaceutical excipients will be followed by an explanation of how the Scheme has been adapted without compromising quality as a result of the COVID-19 pandemic. The use of remote audits within the Scheme will be... Read more » 
Managing the natural variability and contaminants of plant-based pharmaceutical ingredients Stéphanie Bureau Director R&D and Regulatory ADM - SIO Why managing variability? Pharmaceutical ingredients play a key role in drug formulation. Variations in their composition and physicochemical properties can have significant impact on the final drug product performances like safety, physical and chemical stability and... 
Process Engineering and Formulation Focus Group – Academy of Pharmaceutical Sciences Dr Kendal Pitt GSK Manufacturing Classification System: Putting Numbers to Tablet Development Prof Zeeshan Ahmad The Leicester School of Pharmacy De Montfort University Electrically Driven Emerging Technologies for the Manufacture of Pharmaceutical Dosages View On-Demand 
COVID-19: Six Months Later Daniel Chancellor Director, Thought Leadership Informa Pharma Intelligence This fall marks half a year since COVID-19 was officially declared a pandemic, changing our lives forever. While this may seem a lifetime ago, the biopharma response is realistically only reaching the end of the beginning. In this webinar, Pharma Intelligence reviews the... 
Innovation in Medicines Manufacturing via the MMIC Dr David Berry CPI View On-Demand 
Nitrosamine Testing – Removing The Roadblocks Dr Daniel Nicolau Technical Specialist in Impurities RSSL Are you hitting roadblocks with your Nitrosamines Impurity Analysis? To help you maximise your expertise and capability we will be discussing the appropriate sample preparation that ensures suitably extraction of relevant nitrosamine impurities to complement your analytical methods, helping you to... 
View On-Demand Filling the gap in continuous pharmaceutical technologies: A novel continuous filtration drying system Simon Coleman Product Manager – Isolation and Drying AWL The Importance of Process Simulation in the Pharma Industry Sam Fass Communications Coordinator at IChemE Process Engineer at BPE Design and Support Plug and Play for Biopharmaceutical Operations Keith Morris Automation... 
Bridging The Gap Between Discovery and Development – DMPK Influence Richard Weaver XenoGesis Ltd Bridging The Gap Between Discovery and Development – DMPK Influence Working with your CRO: Creating perfect research partnerships in an imperfect research world Nicola Wall Afortiori Development Working with your CRO: Creating perfect research partnerships in an imperfect research world View... 
E-PI's; Using Smart Packaging Systems to Improve Patient Outcomes and Increase Sales Through Enhanced Communication Chris Waterhouse Packaging Collective View On-Demand 
The Role of Excipients in Paediatric Formulations Kevin Hughes IPEC Europe View On-Demand 