If you are seeking an opportunity to apply your clinical project management skills to a different research environment, CSL have a role that will spark your interest. CSL client is a world leader in outcomes research studies and is now expanding their team as a result of continued business growth. CSL [...]
Clinical Trial Associate required for initial 12 month contract role in Hampshire. CSL Global Pharma client is looking for a CTA/CPA with at least 12 months clinical research experience working as a clinical trial administrator within a pharma, biotech or CRO. Main Duties: Provide efficient clinical trials administrative support across Phase II [...]
The Resource which I’m going to mention is one of the best for the computational chemistry. It is CCL, Computational Chemistry List. It was established on January 11, 1991, as an independent
Superb role now open for a capable PhD or Medical Doctor with industry expertise in Translational Medicine or Clinical Pharmacology to drive forward this company’s exploratory programmes in Man. Outline Duties: Interact directly with the company’s discovery and clinical pharmacology departments to assist in the transition of compounds from the bench to the clinic Directs [...]
The ISPE 2010 Washington Conference brings together all levels of pharmaceutical industry professionals to network and benefit from a variety of seminars and trainings. Washington Conference features practical applications, results orientated workshops, and a special FDA-ISPE collaboration on Pharma Quality Systems.
Russell J. Greene, Norman D. Harris, “Pathology and Therapeutics for Pharmacists, 3rd Edition”
Pharmaceutical Press | 2008 | ISBN: 085369690X | 982 pages | PDF | 8,4 MB
This is the textbook for undergraduate pharmacists which takes an integrated approach to the pathophysiological and pharmacotherapeutic principles underlying the treatment of disease.
Aminoglycoside Antibiotics: From Chemical Biology to Drug Discovery
Publisher: Wiley-Interscience | ISBN: 047174302X | edition 2007 | PDF | 339 pages | 10,5 mb
During the last twenty years, there have been numerous advances in the understanding of the chemistry, biochemistry, and recognition of aminoglycosides. This has led to the development [...]
This interactive webinar discusses the role of excipients in the US, and their use in the pharmaceutical, dietary supplement and food substance industries. Dr. Malawer looks at functional use categories and general guidance provided in the USP 32–NF 27. He discusses the types of compendial specifications related to the measurement of [...]
Course Description:
Gain insight into USP’s perspective on validating methods as detailed in General Chapters <1225> and <1226>. Learn how to apply specific validation performance parameters, develop protocols, and use statistics to evaluate the data. Understand the distinction between validation and verification, and when it is appropriate to execute [...]
Course Description:
This course will cover instrumentation, method development and method validation for analyses of elemental impurities in pharmaceutical materials currently being tested using USP Chapter Heavy Metals <231>. The course will be taught in light of the elements and limits proposed in the draft chapter <232> Elemental Impurities, with [...]
