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Healthy Eating for a Healthy a Healthy Weight Protignes Conferences is hosting the Obesity & Diet Management Conference at Bali on the 15th & 16th of March 2021. Carrying the theme of ‘Healthy Eating for a Healthy Weight’ we aim to create awareness and understanding regarding obesity and the importance of eating healthy. The Obesity Conference will cover the important topics associated with nutrition, diet and weight management. We have slots available for Speakers, Delegates, Poster authors, Exhibitors. Book your slot at the earliest and avail discounted accommodation in Bali. To promote your organization and collaborate with our obesity event contact us at: Email: hello@protignes.com Ph: +91-8971433223 http://obesity.protignes.com/index.php
Protignes Obesity and Diet Management Summit
07-Dec-2020 - 08-Dec-2020
PPMC 2020 presents a platform for the sharing & interaction of latest advancements between experts in the fields of pharmaceutics, drug delivery, biotechnology, nanotechnology from all over the globe. It aims to share some unique research by providing holistic exposure to cutting-edge technologies and challenges in the field of pharma & public health. The conference opens the doors for many researchers in academia, clinicians, and industry representatives working in these exciting areas. The esteemed event typically incorporates Keynote talks, Plenary sessions, Workshops and Poster sessions with eminent international experts and scholars. Target Audience: CEO’s, Directors of Pharmaceutical Companies R&D Researchers from Pharma Indus…
Plenareno Pharma Middle East Congress

Cedar Court, White Waltham, Maidenhead, Berkshire, SL6 3LW,

The Course Clinical Trial Administrators are at the heart of any project team and play an essential role in the clinical trial process. This course gives an in-depth look into some of the aspects of clinical trials. It aims to give an understanding of the history and evolution of clinical research.Delegates will be guided through the essential documents required at each stage of the clinical trial process and their respective functions, an outline of the key roles and functions, and explores how the role of the CTA fits into the clinical trial process.The course also gives further insight into the EU legislation governing trials, ethics committees, audits and inspections, using and creating SOPs, auditing and archiving. The course will utilise trainer input, exercises, and delegate interac…
24-Nov-2020 - 24-Nov-2020

Cedar Court, White Waltham, Maidenhead, Berkshire, SL6 3LW, England

The Course Do you want to work SMARTER not HARDER?  This course is focused on the needs of a clinical researcher and is a very practical course with exercises and methods to build and develop the core soft skills to allow you to work more efficiently and increase your productivity. Oftentimes issues arise due to communication breakdown.  We look at how information should flow within project teams and examine when different types of communication are most effective. We all work to tight deadlines, but do you find yourself wondering where your day has gone?  Our trainer will help you examine your working practices to enable you to set goals, prioritise activities and develop an effective working plan, while keeping your eyes open for those time thieves.   Learning Objec…
23-Nov-2020 - 24-Nov-2020
Asian Public Mental Health Congress 2020 pertains to Psychiatry and Mental Health Disorders such as anxiety, depression, bipolar, behavioral disorders, post-traumatic, seasonal depression, persistent depressive disorder, stress and understanding the effective diagnosis & treatment to identify and help to facilitate the recovery of someone suffering from psychiatric disorders. Target Audience: Clinical Psychologists Psychopharmacologists Mental Health Professionals Neuropsychiatrists Neurophysiologists Neuropathologists Counselors and Social Workers Healthcare Professionals in the Behavioral Sciences
Asian Public Mental Health Congress

Cedar Court, White Waltham, Maidenhead, Berkshire, SL6 3LW, England

The Course This practical course defines the role of the clinical research monitor and explains the interaction with others in key roles as part of the clinical trial process as well as exploring the more complex aspects of clinical trial monitoring. Guidance will be given on best practices for selecting investigators, conducting monitoring visits and safety reporting. Delegates will explore strategies for dealing with common clinical trial management issues and how to adopt a preventative approach to handling monitoring issues. The course uses a blend of trainer input, exercises and delegate interaction. Learning Objectives • Define the roles and responsibilities of Monitors, Sponsors, Investigators and Ethics Committees • Describe the key criteria for selecting investigators • Summarise…
18-Nov-2020 - 20-Nov-2020
This meeting aims to develop our understanding of the potential of liquid biopsies. This includes to support early detection of cancer; as prognostic, pharmacodynamic and predictive biomarkers of treatment efficacy and resistance; and for patient monitoring, including of minimal residual disease for early identification of disease relapse. It will also explore how liquid biopsies can be incorporated in cancer patient management and how implementation of liquid biopsies can change clinical practice.
“36th World Vaccines and Immunization Congress” mainly focuses on the gathering and concentrate on the trending advances and development in every aspect of Vaccines and Immunization research which takes an opportunity in meeting, organizing and see the new logical advancements of the specialists and researchers. We foresee a great scientific faculty from Australia and in addition from different nations with some highly interesting scientific researchers to delegate the occasion. We unconditionally invite all the prominent Researchers, Professors, Students and delegates to participate in this upcoming Vaccines and Immunization event to witness a valuable scientific occasion and to participate in Vaccines Workshop, Vaccines Symposium & contribute to the future innovations in the field of…
36th World Vaccines & Immunization Congress
18-Nov-2020 - 18-Nov-2020

41, Münchensteinerstrasse, Basel, 4052, Switzerland

This one-day course provides a general overview of the clinical research process, regulations, terminology, acronyms as well as roles and responsibilities within the clinical research setting. The following topics will be covered: • Developing a drug in the pharmaceutical industry – from the idea to the product you buy in the pharmacy – and the contributions of clinical research• What is a clinical study – the four phases of clinical development• Who are the key players and what are their roles in the process• The language and abbreviations the clinical research team are using every day• What are the rules, guidelines and laws that need to be followed and why are they so important• How is a clinical study performed – from preparation over conduct to termination of a study• A key to a succe…
Introduction to Clinical Research
17-Nov-2020 - 17-Nov-2020

Cedar Court, White Waltham, Maidenhead, Berkshire, SL6 3LW, England

The Course Statistics is the art and science of summarising data.  Statistics play an essential role in all stages of clinical research from design through to analysis and interpretation.  Clinical Trials generate large volumes of data but most of us are looking for the “punch-line”;  Did the new treatment work?  Were the two groups being compared the same of different?  We rely on statistics to help us design the most appropriate trial to answer our questions, to determine the required sample size and to interpret the results.  A poorly designed study wastes time, resources and puts patients at unnecessary risk.  A solid understanding of statistical principals is important for all team members, not just the team statistician; however for many of us stati…

Cedar Court, White Waltham, Maidenhead, Berkshire, SL6 3LW, England

The Course This practical course provides delegates with basic project management techniques that can be applied to clinical trial project management. Learning is through a combination of trainer input, discussion groups and exercises. There will be a workshop where delegates will develop a plan for tracking and managing a clinical trial case study. Delegates will receive a comprehensive course workbook. Learning Objectives • Define basic project management terms • Create a work breakdown structure and task network • Develop a skills matrix • Define a project schedule and conduct critical path analysis • Analyse resource requirements • Describe and apply a process for managing risks • List the common parameters that need managing and tracking • Outline a general process for dealing with v…
09-Nov-2020 - 11-Nov-2020
Leaders in Healthcare | 9-11 November 2020 | LondonBrought to you by FMLM and BMJ, the Leaders in Healthcare conference returns to the Barbican, London on 9-11 November 2020 and the affiliated Masterclass day on 11 November, which will be held at a central London venue.  Over three days, this conference will bring together over 800 attendees with an interest in leadership, from aspiring leaders to senior level managers and directors, to hear from 100+ inspiring speakers from around the world to discuss the future challenges and opportunities in healthcare. Who attends?Delegates consist of healthcare colleagues from all professions, career stages and specialties, who want to improve patient care and outcomes through effective leadership. How to bookTake advantage of our early bird rate…
Leaders in Healthcare 2020
04-Nov-2020 - 04-Nov-2020

TBC, TBC, University of York, York, York, YO10 5DD, United Kingdom

The demand for public health interventions is growing as the NHS and social care system tries to ensure future sustainability. NHS, social care and public health organisations are expected to be able to economically justify any changes in care pathways they propose and there are concerns not only around cost-effectiveness but also the affordability of new initiatives. Many public sector bodies are under pressure to achieve efficiency and productivity savings in order to balance budgets. They are seeking innovations that will reduce cost pressures and they need to understand the impact of changes in different sectors, including primary, community and social care as well as acute care. There is a focus on primary and secondary prevention approaches in public health to try to reduce demand ac…

Cedar Court, White Waltham, Maidenhead, Berkshire, SL6 3LW, England

The Course Approximately 1.5 million different medical devices are available globally; with thousands of new and innovative medical devices being introduced to the market every year. While there is legislation at the national and regional level ISO 14155 provides a global standard for clinical investigations on human subjects.   In this course we explore ISO-14155 in detail.  ISO 14155:2011 addresses good clinical practice for the design, conduct, recording and reporting of clinical investigations carried out in human subjects to assess the safety or performance of medical devices for regulatory purposes.  This International Standard specifies general requirements intended to: • Protect the rights, safety and well-being of human subjects • Ensure the scientific conduct of t…
29-Oct-2020 - 29-Oct-2020

Cedar Court, White Waltham, Maidenhead, Berkshire, SL6 3LW, England

The Course This course provides an in-depth look at the regulatory systems currently in operation in the EU and their impact, together with UK legislation, on the conduct of clinical research. Starting with a refresher on the history of medicinal product regulations and the need for ethics, the course explains in more detail the practical applications of GCP and outlines recent major developments in GCP. It also explores the impact of EU data protection laws on clinical research and summarises other current issues that affect clinical trials. Delegates will receive a complimentary copy of the ICH GCP guidelines and a workbook. Learning Objectives • Outline recent major developments in Good Clinical Practice • Discuss the purpose and impact of EU regulations on the conduct of clinical re…
J35 GCP for Experts
20-Oct-2020 - 20-Oct-2020

41, Münchensteinerstrasse, Basel, 4052, Switzerland

In an increasingly cost-conscious health care environment, pharma companies must make a thorough case for not only the clinical, but also the economic value of their products. This  one-day course provides an introduction to the Pharma Market Access dynamics and challenges.
Understanding Pharma Market Access
20-Oct-2020 - 21-Oct-2020

Cedar Court, White Waltham, Maidenhead, Berkshire, SL6 3LW, England

The Course In this highly practical course we look at the root cause of typical inspection findings and work with delegates to develop personal corrective and preventative action plans. Through case studies, we will address challenging monitoring situations and develop strategies for investigator selection, fraud detection, improving patient recruitment and for motivating investigator sites. Delegates will explore how both technology and legislation will impact the role of the monitor. We also discuss key principles in project planning and execution to allow experienced CRAs to begin to develop the skills required for a Lead CRA or Clinical Trial Manager role. Delegates will learn how to apply project planning principles to monitoring to improve efficiency. It is recommended that delegate…
J33 Advanced Monitoring

Cedar Court, White Waltham, Maidenhead, Berkshire, SL6 3LW, England

The Course The MHRA GCP Inspectorate has updated their definition of critical to include, ‘where provision of the Trial Master File (TMF) does not comply with Regulation 31A 1-3, as the TMF is not readily available or accessible, or the TMF is incomplete to such an extent that it cannot form the basis of inspection and therefore impedes or obstructs inspectors carrying out their duties in verifying compliance with the regulations.’ This follows numerous issues with inspector access to TMFs and incomplete TMFs. The TMF provides the basis for inspection by the competent authority (2005/28/EC). The UK Clinical Trial Regulations (2004/1031, Regulation 31A) require that the sponsor must keep a TMF and it must be readily available and shall at all times contain the essential documents relating…
J32 Essentials of Essential Document Management; Managing the TMF

Cedar Court, White Waltham, Maidenhead, Berkshire, SL6 3LW, England

The Course An Introduction to Clinical Trials and Clinical Trial Practice, the ICR’s flagship training course, is accredited by Cranfield University. This highly practical course explores the relevance of clinical research in drug development and summarises the ethical and regulatory requirements for clinical trials. It covers clinical trial methodology and summarises the principles of Good Clinical Practice. The course gives an overview of the various aspects of clinical research and will be of interest to all members of the clinical study team. It uses a combination of lectures, tutorials and group workshops. Delegates receive a comprehensive workbook and a copy of ICH GCP guidelines. The content of the course will equip delegates to sit the ICR Certificate examination. Learning Objectiv…
J31 Introduction to Clinical Trials and Clinical Trials Practice
The 2nd EACR Conference on Mechanisms to Therapies: Innovations in Cancer Metabolism will gather top experts in the field to discuss the metabolic alterations in tumours and how we can exploit it to treat cancer. The target audience for this conference is basic and translational scientists and clinicians, both senior and young investigators that want to have a broad and detailed overview of the most recent advances in the field of cancer metabolism.