Science Researcher Update: Spotlight on Meetings, Conferences, and Events
Tags: 2014, Drug Discovery, United Kingdom, pharmaceutical, December, research course, Life Science
Tags: 2014, November, United Kingdom, pharmaceutical, London, Conference, Biotechnology
Tags: Healthcare, pharmaceutical, Switzerland, Zurich, 2015, February, Conference, Pharma
Conference - London, United Kingdom
New EU requirements are expected to come into force during 2014, impacting clinical trial processes including informed consent as well as the provision of public access to information and results of clinical trials.
Tags: 2014, United Kingdom, Medicine, Workshop, September, pharmaceutical, clinical trials, Chemical Sciences, Chemistry, London
Course - Opfikon-Glattbrugg, Switzerland
By attending this course, you will:
1. Grasp the entire process of deal-making within the pharmaceutical and biotech industries, and learn the language, the concepts and tools from a practitioner’s point of view.
Tags: 2014, September, Development, pharmaceutical, Switzerland, biotech industry, biotech, Biotech current events, Life Science
Course - London, United Kingdom
The new EU Clinical Trials Regulation is expected to become applicable in 2016.
Tags: 2014, United Kingdom, Medicine, Workshop, September, pharmaceutical, clinical trials, Chemical Sciences, Chemistry, London
Congress - London, United Kingdom
Over the two days this well established congress will bring together over 175 senior experts to discuss the most pressing challenges in Pharmaceutical IT.
Tags: 2014, Pharmacology, United Kingdom, Congress, September, pharmaceutical, London, Life Sciences
Conference - Hong Kong
This course is designed for people who are growing in their knowledge of pharmaceutical quality control practices and regulations.
Tags: 2014, Laboratories, September, Quality Control, pharmaceutical, Hong Kong, Conference
Webinar - Online
Describe the North America Commercial Nuclear successful method used method greater than twenty years and how it is applied in any industry using SOP (controlled and regulated) documents to describe instructions to complete work tasks.
Tags: 2014, Michigan, United States, Webinar, May, Quality Control, pharmaceutical, Life Sciences, Conference, MI
Webinar - Online
The ISO 12971 standard on risk management for medical devices describes risk analysis tools such as PHA, FTA, FMEA, HAZOP, and HACCP but does not provide the depth needed to use the tools correctly.
Tags: 2014, Medical Device Technology, Michigan, United States, Webinar, May, Quality Control, pharmaceutical, Life Sciences, Conference, MI