Subscribed Libraries
Pharmacy Pharmacy Video
| Department | Title | Author | Short Description | Video Url |
|---|---|---|---|---|
| Pharmacy | Pharmaceutical Quality Control Testing, | Lucideon | Lucideon’s pharmaceutical quality control testing and validation laboratories are fitted with state-of-the-art analytical equipment and testing facilities. | https://www.lucideon.com/healthcare/pharmaceuticals/pharmaceutical-quality-control-testing |
| Pharmacy | Order processing and manufacturing of liquid medicine | Da N | General overview of Order processing & Manufacturing of liquid medicine in a pharmaceutical manufacturing company. This video is for educational purposes and no copyright infringement is intended. Sound recordings, musical components and the majority of the video content are the property of the user. We urge viewers not to abuse medicine and/or drugs. | View |
| Pharmacy | Peptide bond formation | Khan Academy | How amino acids form peptide bonds (peptide linkages) through a condensation reaction (dehydration synthesis). | View |
| Pharmacy | Pharmaceutical Nanotechnology Applications | Microfluidics International Corporation | Solve Pharmaceutical Nanotechnology Application Challenges from Development to Production. | View |
| Pharmacy | Injectable formulations | HCPLive | In this segment of the Peer Exchange, the panelists discuss some investigational HIV agents that are available in injectable forms. | https://www.hcplive.com/view/investigational-hiv-drugs-and-injectable-formulations |
| Pharmacy | Mechanistic long-acting Injectable Model for PLGA Polymer Implants | Certara | Long-acting injectable (LAI) delivery methods have proven to be beneficial for a range of drug types and situations, including CNS drugs (patient adherence), hormone therapy for oncology, women and men health and HIV to name a few. Certara has developed a mechanistic PLGA polymer-based model for assessing drug distribution and performance of these formulations. In this webinar, the model for solid implant, in-situ gel implant, and microsphere depot implants was covered. These models have been used for regulatory submittal of novel drugs and complex generics. Case studies of tacrolimus and leuprolide were also shared | View |
| Pharmacy | The importance of the formulation (galenic) of feed additives | Feed channel | 1 A chemist in the Feed industry: Safety first!, #2 The importance of the formulation (galenic) of feed additives, #3 Chemistry and Biotechnology: the future for the Feed industry | https://www.feedchannel.online/the-importance-of-the-formulation |
| Pharmacy | Regulatory Affairs | Industry Pharmacists | International Drug regulatory Affair | View |
| Pharmacy | The FDA Drug Development Process: GLP, GMP and GCP Regulations | GlobalCompliance Panel | This Video provides an overview of the FDA’s Drug Development Process. This webinar also includes the major FDA regulations involved in the Drug Development Process – the GLP, GMP and GCP regulations. This Video is ideal for those who are new to the Drug Development process and those experienced researchers that need an update on FDA requirements. This webinar will address the basic Drug Development Process, nonclinical trials and human clinical trials. In addition the two major FDA submissions during Drug Development will be covered – the IND submission and the NDA submission. | View |
| Pharmacy | U.S. FDA eCTD Requirements for Drug Master Files (DMFs) | Registrar Corp | Beginning May 5, 2018, the U.S. Food and Drug Administration (FDA) will require DMFs and DMF submissions (amendments, annual reports, etc.) to be filed in electronic common technical document (eCTD) format. Any paper submissions filed on or after this date will be subject to rejection. There will be no waivers or exemptions for submitting DMFs in eCTD. | View |
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