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Pharmaceuticals/Drug Discovery Conferences

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  1. Jun 23 2014

    Essensials of European Regulatory Affairs

    Gain an overview of the European Network, Marketing Authorisation for Medicinal products in the EU and Lifecycle Management.

    The course will give an overview of the European regulatory system, including the legislative processes and European Networks, the different routes for obtaining a licence for the European market, the centralised, the decentralised and the…

  2. Jun 18 2014

    Clinical Governance

    With 1320 public hospitals, private hospitals and day procedure centres being audited over the next four years.
    In Sydney (Australia)

    It is vital all healthcare organisations effectively embed the national standards. Hear case studies from leading organisations on how to manage ongoing audits and stengthen clinical quality at all levels. Participate in interactive panel discussions…

  3. Jun 17 2014

    The Patients Summit

    The Patients Summit is the definitive meeting point for pharma to discuss how it's serving patients and will provide you with the tools to build trust and add v

    Pharma has recognised that to keep up with the competition and truly deliver a superior service to patients, it needs to offer more than just a pill. Pharma needs to understand how it can better serve its patients, but also that by partnering…

  4. Jun 10 2014

    Pharmaceutical Packaging and Labelling Summit

    Capitalise on patient safety, maximise artwork capabilities, protect your supply chain while preparing for the Falsified Medicines Directive.
    In Basel (Switzerland)
    Venue: Hilton Basel

    Implementing track and trace and serialisation across multiple geographic jurisdictions where strict regulatory requirements differ is just one of the major challenges facing the packaging and labelling industry today. The constant fight to…

  5. Jun 11 2014

    10th Pediatric Clinical Trials

    Utilizing Modeling and Simulation to Design a Pediatric Clinical Trial that will be Compliant with FDA and EMA Regulations

    The 10th Pediatric Clinical Trials Conference will provide executives with successful tools and best practices to effectively submit a PIP that meets FDA and EMA regulations, leverage clinical pharmacology data into data used in a pediatric…

  6. Jun 11 2014

    Big Data & Analytics For Pharma

    Harness the Power of Information

    The Big Data & Analytics for Pharma summit brings together leading industry executives, sharing unique insight into the innovations that are driving success in their organisations. Hear from leading experts and gain insight into the analytics…

  7. Jun 10 2014

    5th Annual Clinical Trials Summit 2014 "A critical guide for successfully conducting clinical trials” 10th & 11th June 2014, Kohinoor Continental Hotel, Mumbai, India For more info on the event and for event brochure kindly visit – http://www.virtueinsight.com/pharma/5th-Annual-Clinical-Trials-Summit-2014/…

  8. Jun 04 2014

    EU and US Requirements for Pharmaceutical Labelling & Package Leaflets

    This interactive three-day course will clarify the European regulatory requirements for developing labelling and package leaflets.

    In the face of increasing regulatory and consumer demand, the need for accurate and complete product information has never been stronger. This course will provide you with key practical information on devising successful labelling strategies…

  9. Jun 03 2014

    Advanced CMC Analytical, Comparability and Stability Studies for Biotechnology and Biosimilar Products

    This course will teach delegates to improve strategies for complying with complex regulatory guidelines, and to ensure compliance and increase efficiency.

    This class is designed to follow PTI's introductory level course, but may also be taken as a stand-alone class for attendees with experience in aspects of biotechnology. Details will be presented on technical issues in designing and executing…

  10. Jun 02 2014

    How to Develop Stability Indicating HPLC Methods

    How to Develop Stability Indicating HPLC Methods
    In London (United Kingdom)

    Pharmaceuticals need to be assessed for stability to support the assigned shelf life. Therefore, when analysing stability samples obtained from these studies analytical methods are required which are stability indicating, i.e. there is a measureable…

  11. May 30 2014

    Transfer of Analytical Methods for Pharmaceutical Analysis

    Transfer of Analytical Methods for Pharmaceutical Analysis

    Transferring an analytical method from one laboratory to another should be straightforward but unfortunately it is a process which is often problematic. Recognition of this has resulted in a new USP chapter and an update to chapter 6 of the…

  12. May 29 2014

    7th Annual Pharmaceutical Law Conference 2014

    Don't miss your opportunity to receive top-quality guidance on the latest legal and regulatory hurdles facing the pharmaceutical industry.

    2014 HIGHLIGHTS . UNIQUE FOCUS SESSIONS: Pharma Law Reform, IP, Competitive Strategies, Industry Transparency . INTERACTIVE DEBATES focused on Sustainable Drug Pricing and Patenting Life Sciences . NEW INTERNATIONAL updates and perspectives…

  13. May 28 2014

    Validation of Analytical Methods for Pharmaceutical Analysis

    Validation of Analytical Methods for Pharmaceutical Analysis

    The data generated using analytical methods is essential for many of the critical decisions made in the pharmaceutical industry. To be confident in the reliability of this data it is crucial that the methods are fit for purpose. Analytical…

  14. May 29 2014

    Background The Pharmaceutical Supply Chain Initiative (PSCI) is an initiative of the major brands in the pharmaceutical sector. PSCI is a group of pharmaceutical companies that share a vision of improved social, economic and environmental outcome…

  15. May 27 2014

    Mastering Regulatory and Development Strategies for Generics

    Gain a strategic insight into requirements for developing generics from a global perspective and an overview of the generics market.

    The majority of all pharmaceutical company revenues now face generic competition. This represents an unprecedented growth in the generics market. With more and more patents expiring since 2006, this global expansion looks set to continue. Bringing…

  16. May 26 2014

    Advanced Regulatory Affairs for Agrochemicals

    This intensive course will challenge participants to build on existing regulatory strategies in order to improve efficiency and shorten timelines.

    Over 3 days this course will educate attendees with the practical knowledge they need to: -Improve the management behind a dossier -Understand what the Regulators want in terms of data -Plan for changing data requirements and consider financial…

  17. May 20 2014

    Biosimilars Asia 2014

    Collaborative Development and Successful Commercialisation

    China remains an attractive destination for MNCs and regional pharma players for biosimilars development. Risks are reduced through strategic alliances and partnerships with local Chinese manufacturers. While partnering with local China companies…

  18. May 21 2014

    World Pharma Congress

    Tackling Translational Challenges

    After spending 12 years in Philadelphia the World Pharma Congress is moving to Boston, which is buzzing with new findings and technologies that can potentially revolutionize the way in which traditional preclinical drug discovery is done. World…

  19. May 22 2014

    Property-Based Drug Design

    Designing the Right Physicochemical and Bio-physical Properties for Improved Developability

    One of the most challenging aspects of drug discovery remaining is the identification of new molecular entities (NMEs) with the desirable physicochemical properties and absorption, distribution, metabolism, and excretion (ADME) profiles that…

  20. May 22 2014

    Chemical Biology for Target Validation

    Minimizing Molecular & Biological Attrition by Interrogating Target-Phenotype Relationships

    Small molecule drug discovery has approached a critical junction where the rigorous pre-clinical validation and prioritizing of novel targets is of utmost importance. Challenged with thinning development pipelines and significant losses in…

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