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Pharmacy Pharmacy Video
| Department | Title | Author | Short Description | Video Url |
|---|---|---|---|---|
| Pharmacy | Titel ORAL THIN FILMS (OTF) | LTS Lohmann Therapie-Systeme AG (EN) | Oral thin films are a modern dosage form that enable rapid and precisely dosed delivery of active ingredients without the need of supplementary water. Our video gives insights how OTFs are designed and how they work. | View |
| Pharmacy | Oral thin films – a new evolution step for active substances | LTS Lohmann Therapie-Systeme AG (EN) | Oral thin films contain the active substance as a film, which is taken orally and is dissolved immediately in the mouth or applied to the mucosa. For transmucosal films, the active substance enters the bloodstream directly via the oral mucosa, without having to first pass through the gastrointestinal tract. | View |
| Pharmacy | Gene Delivery Systems for Gene Therapy – Creative Biolabs | Creative Biolabs | One of the key steps in gene therapy is to deliver foreign genes or gene editing systems into target tissues or cells. Thus efficient gene delivery system is very important to the effect of gene therapy. We discussed the gene delivery systems that commonly used in research and clinic, and our gene delivery system development services. | View |
| Pharmacy | Gene Therapy | Types of gene therapy | Applications of gene therapy | Dr. Neeraj Kumar | In this video, you will learn about: 1. Gene therapy and it’s types. 2. Virus mediated and Direct methods of gene delivery. 3. Applications, advantages and disadvantages of gene therapy. 4. Major achievements of gene therapy. 5. Future prospects of gene therapy. | View |
| Pharmacy | Pharmaceutical Regulatory Affairs | NPTEL – Special Lecture Series | Regulatory Affairs- RA, in a Pharmaceutical industry, is a profession which acts as the interface between the pharmaceutical industry and Drug Regulatory authorities and Ministry of Health across the world. It is mainly involved in the registration of the API, Finished Pharmaceuticals, Medical Device etc in India and Global countries prior to their marketing. The Regulatory Affairs- RA Department, Act as a liaison with Global Regulatory Agencies and Ministry of Health for Product Registration . It Involves Preparation of organized and scientifically valid Technical DOSSIERS which adheres and is compliant with all the applicable cGMP, ICH, GCP, GLP guidelines, regulations and laws. Providing expertise and regulatory intelligence in translating regulatory requirements into practical workable plans. Advising the companies on regulatory aspects and climate that would affect their proposed activities. Apart from the above main roles, there are various other roles which Regulatory Affairs professionals play. Proficiency in Regulatory Affairs has high Career Prospects for budding Pharmacy Students. | View |
| Pharmacy | Regulatory and Clinical Affairs Alumni Career Paths 2021 | UCSF Office of Career and Professional Development | Regulatory and Clinical Affairs Alumni Career Paths Panel featuring UCSF alums Patrick Heiser, PhD and Brandi Saunders, MS in conversation with Michael Matrone, PhD, associate director, the Office of Career and Professional Development at UCSF. Recorded as part of the Every Month Series. November 2021. | View |
| Pharmacy | How to work in Regulatory Affairs (Drug and Medical Devices) | Easy Medical Device | How long to be ready to work in Regulatory affairs? What are the important skills to have to be a good professional? Is the transition from one regulatory field to another difficult to do? She will really provide us all her knowledge on this and also give us some information about TOPRA. This organization can help you to perform this transition and also to improve on your Regulatory Affairs career. | View |
| Pharmacy | The US Drug Master File Process | Regis Technologies, Inc. | Jennifer Stanek describes the US drug master file process at a seminar hosted by Regis Technologies, inc | View |
| Pharmacy | GDUFA II Training – Pre ANDA Program Pre Submission Meetings, Robert Lionberger | Food and Drug Administration | The pre-ANDA program is new in GDUFA II and it’s designed to accelerate access to generic versions of complex products. Meetings between FDA and ANDA applicants are a critical step toward meeting these goals. | View |
| Pharmacy | Specialty spotlight – clinical pharmacology and therapeutics | Royal College of Physicians | Listen to Dr Reecha Sofat, Senior Lecturer, UCL and Honorary Consultant in Clinical Pharmacology and Therapeutics, UCLH discuss her specialty with Dr James Fullerton, NIHR Clinical Lecturer, UCL and Specialist Registrar in Clinical Pharmacology and Therapeutics, UCLH. | View |
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