Over the past 23 years IIR's Partnerships brand has been the cornerstone for thousands of clinical executives to partner, learn, and innovate across the clinical trial ecosystem. This year we are thrilled to introduce you to the all-new Partnerships in Medical Device Trials Conference, an extension of the Partnerships brand, taking place June 2-4, 2014 in Chicago, IL. The Partnership in Medical Device Clinical Trials conference is specifically...

SMi's 3rd annual Antibody Drug Conjugates Summit comes at the perfect time to focus on innovative manufacturing techniques, preclinical and clinical data and next generation ADCs, bringing together key industry experts from academia, pharma and biotech companies.Join us and hear case studies, presentations and round tables demonstrating how to maximise the therapeutic index of your ADC and how this form of empowered antibody is transforming ne...

It is now nearly two years since the implementation of the new EU Pharmacovigilance (PV) legislation, and so it is time to reflect on the impact these changes have had on the role of the Qualified Persons for Pharmacovigilance (QPPVs) and their position and relationship with Marketing Authorisation Holders and regulatory agencies. QPPVs face multiple challenges, and the 2014 meeting will provide insights from regulators as well as MAH manageme...

The 11th High Content Analysis conference, featuring an array of leading international speakers, this event aims to provide you with an insight into the latest developments. SELECTBIO is pleased to present the 11th High Content Analysis conference, which will take place at the Fira Barcelona, on May 14th and 15th 2014. Featuring an array of leading international speakers, this event aims to provide you with an insight into the latest developme...

The European Conference on Rare Diseases and Orphan Products (ECRD) is the unique platform/forum across all rare diseases, across all European countries, bringing together all stakeholders: patients’ representatives, academics, health care professionals, industry, payers, regulators and policy makers. ECRD covers research, development of new treatments, healthcare, social care, information, public health and support at European, national...

The conference will allow you to Understand cross border regulatory requirements, the impact of the pending EU regulations, consent, efficient storage and tracking strategies to ensure quality will allow you to move forward with your research and improve your drug discovery process.We bring together leaders from industry, academia and institutions from across the globe facilitating learning and development to maximise your research opportuniti...

This course will help you understand the budgeting process, share best practice, facilitate cross-company collaboration, define fair market value and standardise your business' clinical grant process.This essential 2-day course provides you with the necessary skills to formulate and implement a successful clinical trial budget.*Build a successful, cost-effective budget plan for your clinical trial programme*Gain a thorough understanding of bud...

Join us at this year's Medical Device & Manufacturing Texas event to enhance your knowledge and understanding of the latest MedTech industry innovations and emerging technologies.The Nation's Most Trusted Resource for Medical Device Design & Manufacturing Returns to Texas! -Enhance your knowledge and understanding of the latest industry innovations and emerging technologies -Benefit from live presentations from leading industry experts...

The World Heart Federation looks forward to welcoming you to Melbourne, Australia for the World Congress of Cardiology 2014 (WCC 2014) taking place from 4-7 May 2014: A global platform for cardiovascular disease specialists and public health professionals to share knowledge and network with their peers World leading experts presenting 150 sessions on cardiology, policy and public healthLatest scientific findings featured in over 1,000 new abs...

Cphi's Design of Experiments workshop is a 2 Day programme and will provide practical Doe knowledge suitable for those involved in carrying out experiments while undertaking Api r&d, improving processIt is 2 day hands on workshop for Api r&d and quality professionals from pharmaceutical and Api manufacturing companies on implementation of Doe. The speakers would be international Doe experts who will be leading a practical workshop for...