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Pharmaceuticals/Drug Discovery Conferences

Showing 1 - 20 of 2412 listings for Pharmaceuticals/Drug Discovery

  1. Sep 18 2014

    8th Neurodegenerative Conditions Research & Development Conference

    The 8th Neurodegenerative Conditions Research & Development Conference

    It is our pleasure to announce the 8th Neurodegenerative Conditions Research & Development Conference, to be held on September 18-19, 2014 in San Francisco, CA to discuss the latest scientific discovery in the neuroscience field. The drug discovery…

  2. Sep 17 2014

    4th Annual Pharmacovigilance, Risk Management & AER Conference

    Developing Proactive Pharmacovigilance and Risk Management Strategies to Comply with Regulatory Standards and Minimize Risk

    The 4th Pharmacovigilance, Risk Management & AER Conference will address many pressing concerns regarding drug safety, including effectively identifying and managing potential risks and ensuring a balanced benefit-risk ratio. Top pharmaceutical…

  3. Sep 15 2014

    Leaders in Biobanking Congress 2014

    Maximizing Your Investment in Biospecimens

    Today, biospecimen collections are used by multiple research groups for varying research aims, from basic research through clinical trials. A well-managed biobank is a critical prerequisite for high-quality biological research. The proper collection,…

  4. Sep 15 2014

    Cancer Vaccines

    The 3rd annual Cancer Vaccines Conference returns to London on 15th and 16th September 2014 to mark the path forward in terms of cancer vaccine research.

    SMi Group have worked closely with an expert speaker panel which includes KOLs from Amal Therapeutics, Amgen, DanDrit Biotech, CureVac and Vaccinogen, to put together an exciting conference agenda for the 3rd annual Cancer Vaccines conference…

  5. Sep 15 2014

    Webinar On Risk Management Principles

    This course provides an understanding of the basic principles and background to risk management

    ICH Q9 Quality Risk Management issued in 2009 laid out the basic principles for risk management to be utilized in all areas of the pharmaceutical industry including clinical trials but also manufacturing, computer system validation etc.. Taking…

  6. Sep 11 2014

    CHFA East 2014 is Canada’s largest conference and trade show for the natural health and organics industry. It’s the place to meet the industry’s top manufacturers, distributors and brokers, face-to-face. With more than 650 exhibits on our 80,000…

  7. Sep 12 2014

    Webinar on Quality by Design (QbD) Across the Product Lifecycle

    This webinar will demonstrate how to integrate those QbD principles into a pharmaceutical quality system.

    As stated in Q8, the ICH guidance document on pharmaceutical development, drug product should meet its intended product performance as well as meet the needs of patients. Although the strategy for pharmaceutical development may vary from company-to-company…

  8. Sep 12 2014

    Webinar On FDA’s Expedited Programs for Serious Conditions – Drugs and Biologics

    A must attend webinar for those personnel that require an understanding of the FDA’s expedited programs for serious conditions.

    This webinar will discuss four FDA programs intended to facilitate and expedite development, review and approval of new drugs to address unmet medical needs in the treatment of serious and life-threatening conditions. This includes FDA’s newest…

  9. Sep 07 2014

    EFMC-ISMC 2014 - XXIII International Symposium on Medicinal Chemistry

    EFMC-ISMC is one of the leading Medicinal Chemistry meetings, covering drug discovery advances in the major therapeutic areas

    The XXIII International Symposium on Medicinal Chemistry (EFMC-ISMC 2014) will be organised by the Group of Medicinal Chemistry of the Portuguese Chemical Society (SPQ) on behalf of the European Federation for Medicinal Chemistry (EFMC). The…

  10. Sep 10 2014

    5th Generic Medicine, Dubai

    5th Generic Medicine, Dubai

    The Objectives of this conference are: 1. Discuss new developments in Generics and Biosimilars regionally over the last 12 months. 2. Bring together Key Opinion Leaders in the Gulf and Middle East from pharmaceutical companies, CEO’s of hospitals…

  11. Sep 09 2014

    Analytical Method Development, Validation and Transfer

    A dedicated forum focusing solely on new method development, validation and transfer for pharmaceutical and generics man

    Informa life Sciences Analytical Method Development, Validation and Transfer is a dedicated forum focusing solely on new method development, validation and transfer for pharmaceutical and generics manufacturers. The event is the only of its…

  12. Sep 08 2014

    7th Annual Biorepositories and Sample Management Conference

    Learn how to maximize the value of your biospecimens through quality-driven biobanking.

    Attend the 7th Annual Biorepositories and Sample Management Conference to examine the industry's most pressing topics, benchmark best practices with your peers and ultimately learn how to maximize the value of your biospecimens through quality-driven…

  13. Sep 09 2014

    Processing Individual Case Safety Report (ICSR): workflow in Pharmacovigilance Industry

    How to process Individual case safety reports (ICSR) from different sources in pharmacovigilance operations?

    This webinar will describe how to process Individual case safety reports (ICSR) from different sources in pharmacovigilance operations from compliance, and safety perspectives. A structured methodology for case processing and reporting in drug…

  14. Sep 08 2014

    Webinar On Risk Management and Risk Analysis Techniques in Clinical Trials

    This seminar will provide the basics of clinical trial risk management and analysis techniques and practical tips to clinical trial professionals

    If you are currently involved in clinical trials either as a CRA, project manager, investigator or sponsor, this seminar will provide you with an overview of risk factors in clinical trials and possible ways to mitigate, control, assess impact,…

  15. Sep 04 2014

    Webinar On Current GMP Requirements for Combination Products - Final Rule

    you will be able To understand where the combination products GMP rule applies

    As you know, medical diagnosis, technology, and treatment is very dynamic and is rapidly advancing. New discoveries are made that do not fit the "regulatory mold “and thus require new approaches to regulation. Combination products is one such…

  16. Aug 26 2014

    Live webinar on FDA’s 21 CFR Part 11 Add-on Inspections

    This presentation will cover the scope, status and results of the surveillance inspections and what they may mean for the future of 21 CFR Part 11.

    In December 2010 the FDA began a project to better understand the industry’s adherence (or lack thereof) to 21 CFR Part 11. This involves the add on’ surveillance inspections of the sponsors’ computer systems during the course of the FDA’s…

  17. Aug 25 2014

    Webinar On User Acceptance Testing

    an understanding of the role of users in system validation and covers good documentation practice and the writing of UAT scripts.

    Current regulations expect that all users are appropriately trained and that must include being trained how to effectively perform UAT. This course provides an understanding of the role of users in system validation and covers good documentation…

  18. Aug 18 2014

    5th International Conference and Exhibition on Analytical & Bioanalytical Techniques

    Critical Review on Recent Developments in Analytical & Bioanalytical Techniques

    5th International Conference and Exhibition on Analytical & Bioanalytical Techniques during August 18-20, 2014 at DoubleTree by Hilton Beijing, China. We welcome all the participants from across the world to take part in this premier event.…

  19. Aug 19 2014

    This two-day event will allow all participants the ability to learn about the current market access approaches which are required for each market in order for them to have greater certainty that their products will be able to deliver real value…

  20. Aug 20 2014

    Webinar on Conformance of Design History Files for Mature Medical Devices

    In this webinar, we will discuss practical steps you can follow to bring your product design history files up to current standards.

    This webinar on Design History Files (DHF) will provide a step-by-step procedure for all medical device companies that are in need of bring their product design history files up to date with the current standards. Many medical industry companies…

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