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On behalf of the Organizing and Advisory Committee we take great pleasure in welcoming applied science scientists, chemists, physicists and experts of application fields to Dubai, UAE for the "3rd Global Conference and Expo on Applied Science, Engineering and Technology” conference to foster the progress in the field by contributing with your expertise to what promises to be a very comprehensive and exciting meeting, and to enjoy the immense unique artistic heritage and wonderful landscape of UAE. "3rd Global Conference and Expo on Applied Science, Engineering and Technology” (Applied Science-2019), which will be held during October 07-09, 2019 Dubai, UAE is now an established event, attracting global participant’s intent on sharing, exchanging and…
3rd Global Conference and Expo on Applied Science, Engineering and Technology
07-Oct-2019 - 08-Oct-2019
World Pediatrics 2019 conference aims in gathering renowned Scientists, Professors and Research professionals across the globe under a single roof, where they discuss the research, achievements and advancements in the field. It also catalyzes for information exchange and networking between researchers and business entrepreneurs of diverse backgrounds for the advancement of Technology and Research in the field of Pediatrics.   “32nd World Pediatrics Conference” is an excellent platform to discuss critically important research and to intensify collaborations and scientific research. To know more about the conference, Please follow the link http://worldpediatrics.pediatricsconferences.org/ For any further info / assistance / queries  please do feel free to contact me at any time,…
07-Oct-2019 - 08-Oct-2019
Food Technology Events | Food Technology Meetings | Food Technology ConferencesConference Series LLC LTD has been influential in leading international food events for so many years, and very excited to expand Europe, America and Asia Pacific continents. With the grand success of many food conferences again it’s back with the 23rd International Food Technology and Processing Conference which is going to be held during October 07-08, 2019 in Dublin, Ireland. Food technology and processing reconnoitre the approaches of preparing, packaging and delivering food products to customers. The turf of food technology and processing relates scientific principles to the production and distribution of food. Food technologists often advance new ways to better preserve, process, package, store and de…
Food Technology Conferences
For Sponsorship/Exhibitor enquires, please contact the Conference Manager Join us for the 31st Annual Ironman® Sports Medicine Conference - a must-attend event for medical professionals with an interest in Sports Medicine and treating endurance athletes at all levels. The 2019 Conference takes place October 6-12, 2019 at the Royal Kona Resort, Kailua-Kona, Hawaii.  The Ironman World Championship takes place on Saturday October 12, 2019. Each year, over 200 medical professionals attend this prestigious event, which sells out each year.  In addition to the conference, attendees also have the option to earn additional CME credit by volunteering in the Ironman® Medical Tent on race day. Course Highlights  Twenty Five (25) Hours AAFP CME World-renowned Faculty discussing lead…
2019 Ironman Sports Medicine Conference October 6-12, 2019  Kailua-Kona, HI
05-Oct-2019 - 08-Oct-2019
In Vancouver we have the honor of being the first to incorporate the new focus of the society – that of Cartilage Regeneration and Joint Preservation. To that end, we aim to bring together the three traditional pillars of ICRS – clinicians, scientists and industry partners – to illustrate what we can do collectively, to address the growing need towards addressing joint dysfunction and disability. Musculoskeletal disease is a growing problem and represents a significant burden on society worldwide. The concept of joint preservation not only suggests joint tissue repair, but also improvements in patient function and wellbeing, a subject that we hope to showcase throughout the program. A consistent theme through the meeting will be that of the ‘Next Generation’. This will include the next gen…
Raw material requirements in a cGMP environment are often overlooked as a Company develops new products. Depending upon the product being developed, e.g., tablets and capsules vs. biotechnology products to include recombinant microorganisms and gene therapy products, as few as fifteen to twenty or as many as sixty raw materials need to be sourced before the process can be moved from initiation through completion. This highly interactive two day seminar on raw material requirements in a cGMP environment will: Consider FDA, Health Canada, ICH, USP and EP requirements. Examine a variety of the issues surrounding raw materials to include what materials should be tested and to what extent during Phase 1, 2, 3 and commercial production. Cover testing requirements during each Phase (Phase approp…
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions
Learning Objectives: Identify the required regulations and guidance documents for drug and device submissions Use regulations and guidance documents to outline and construct drug and device submissions Formulate a working knowledge of regulatory submissions, publishing, and style guides Create checklists that encompass timelines and sections needed from contributors Areas Covered: Contents of IND and IDE Regulatory requirements for IND and IDE application process Submissions to IND or IDE to the FDA Establishing communications with FDA Type of FDA meetings Amendments to IND and IDE applications Progress reports for IND and IDE Who will Benefit: Project Managers Clinical Research Associates Data Managers Project Team Leaders with limited direct regulatory experience Grant Administrator…
Investigational New Drug (IND) & Investigational Device Exemptions (IDE) Applications Preparation and Submission, and Conducting FDA Meetings
The course will cover the latest variation regulations and offer guidance from an industry expert on how to optimise your regulatory procedures to help achieve faster approval. Benefits of attending: Gain an overview of the EU system for variations Assess how pharma companies are working in this evolving regulatory environment Profit from practical advice on the preparation and submission of variation applications Understand the impact of Module 3 on your variations dossier Discuss filing tips and strategies to help achieve faster approval
Variations to Marketing Authorisations
Attend this seminar to learn the concepts for developing compliance programs to maintain the validated state. These programs are included in the Six-system Inspection Model of the Facility portion of the FDA Guidance For Industry – Quality Systems Approach to Pharmaceutical Current Good Manufacturing Practice Regulations. Topics include GMP Maintenance, Calibration, Pest Control, Replacement Parts, and Project Engineering/Engineering Document Control. Learning Objectives: To understand the ongoing requirements of facilities, maintenance, and calibration systems to maintain the validated state of equipment and facilities. Understand requirements for a complaint Project Engineering Program Instituting a Compliant Maintenance Program Developing Preventive Maintenance Regimen Hand…
Facility, Maintenance and Calibration Considerations of the Quality Systems Inspection Technique (QSIT)
02-Oct-2019 - 03-Oct-2019
Harness data and tech to engage customers and dominate markets. As consumer attitudes shift to “one-click” pharma needs to shift with it. Improving customer engagement strategies and processes are the key to improving reputations and delivering value. But how do we get there? The answer, we can’t do it alone. The responsibility to deliver an excellent customer engagement strategy sits across several functions, at eyeforpharma Marketing Disruption Summit USA we’ll be going beyond the theoretical and bringing together all stakeholders to deliver a blueprint to revitalize customer relationships. 2019 Expert speakers include: • Anish Shindore, Head of Digital Acceleration, Sanofi• Martina Flammer, SVP, Customer Value, Boehringer Ingelheim• Judith Lyster, Digital/IT Leader Canada, Eli Lilly and…
The Marketing Disruption Summit USA
01-Oct-2019 - 03-Oct-2019
The 8th European Trial Master File Summit is designed to put a focus on technology, processes, strategies, multiple points of view, and more which will allow attendees to gain a robust overview of how to manage, process, and enhance their TMF. Technology is now one of the essential means to establish tools that can assist with processes and resources that are necessary to support the use of the system. With the advent of eTMFs, sponsors are now able to achieve so much more beyond completeness for compliance with their TMF. Automation, machine learning and AI allow for the sorting, accessing, processing and analysing of more data, in less time — improving management oversight and efficacy of your Quality Management System. This year’s event will feature quantity needed over three days, expl…
8th European Trial Master File Summit
30-Sep-2019 - 02-Oct-2019
Meet Regulatory Professionals at the TOPRA Symposium in Dublin Regulatory Professionals, part of the Clinical Professionals Group will be exhibiting at the TOPRA Symposium conference in Dublin, on the 30th September – 2nd October. Regulatory Professionals was founded by The Clinical Professionals Group in 2013 to provide specialist staffing solutions for clients recruiting within the regulatory affairs sector. As part of The Clinical Professionals Group and our parent company CPL Resources Plc, we have a vast network of offices across the UK, Europe and the US so can offer the expertise of a specialist regulatory recruitment agency with localised market knowledge, combined with the international coverage and knowledge of a leading Life Sciences total talent solutions business. Regulatory…
30-Sep-2019 - 01-Oct-2019
With some of the world’s best-known biologics continuing to face patent expiration in the coming years, the biosimilar market is set for continued growth. This seminar will cover the regulatory pathways for both the EU and US and how to develop effective strategies for developing biosmilar products. You will be introduced to key biological requirements and the concept of totality for biological review. Benefits of attending: Discuss global considerations and definitions of biotech/biosimilar products Gain an invaluable overview of the regulatory pathways for biosimilars in the EU and US Understand the key Module 3 dossier requirements for biotech products versus pharmaceutical products Learn how to develop effective strategies for development of biosimilar products
Biosimilars
30-Sep-2019 - 30-Sep-2019
Course Overview We all encounter difficult people in our working life. This one day course is designed to help you deal with those that can, at best, be a minor irritant or in some cases make your working day a misery. By the end of the course you will have: Considered why people are difficult Acquired hints and tips on how to deal with the dominators, the manipulators, the negatives and the obstacles Analysed the attributes needed for dealing with difficult people and acquired some damage limitation strategies Practised good questioning and listening techniques Developed a plan to cope with your own difficult people Book both This meeting runs back-to-back with Conflict Management and there is a further £100/€140 discount when booked together. Who should a…
Data integrity is now a focus for regulatory inspections, with both EU and FDA inspectors increasingly observing violations during GxP inspections. It has become a critical issue in document governance and regulators expect staff working in GxP roles to have been trained in this important area. This concise course covers the background to data integrity, why it is important and how its requirements affect both paper-based and computer-based systems. The course will include discussion of the recently finalised MHRA data integrity guide which provides guidance on the data integrity expectations that should be considered by organisations involved in any aspect of the GxP pharmaceutical lifecycle (GCP, GMP, GLP and GvP). You will gain an understanding of the requirements for ensuring data int…
Data Integrity and Document Management
Course Overview Data integrity is now a focus for regulatory inspections, with both EU and FDA inspectors increasingly observing violations during GxP inspections. It has become a critical issue in document governance and regulators expect staff working in GxP roles to have been trained in this important area. This concise course covers the background to data integrity, why it is important and how its requirements affect both paper-based and computer-based systems. The course will include discussion of the recently finalised MHRA data integrity guide which provides guidance on the data integrity expectations that should be considered by organisations involved in any aspect of the GxP pharmaceutical lifecycle (GCP, GMP, GLP and GvP). You will gain a…
Under the theme 'Entering a New Era for Market Access', this year's Summit will explore the future of drug pricing from a balanced perspective. The rebate system, new powers for Medicare Part D, global factors that could affect the pricing and market access landscape in the US, as well as the effects of public pressure and President Trump's Blueprint to Lower Drug Prices. will all be examined under the chairmanship of Sarah Neville, Global Pharmaceuticals Editor of the Financial Times.
FT Pharma Pricing and Value Summit 2019
The Congestive  Heart  Failure  Congress  is going to be held in Florence, Italy during September 26-27, 2019 under the theme: "Prediction and Prevention of Heart Failure'' which is going to be organized by Conference series LLC Ltd. The organizing committee is preparing for an informative, exciting conference including lectures, symposia, workshops on a wide variety of topics through oral, poster presentations by the participants across the globe. We invite you to join us at World Heart Failure 2019 where you will be sure to have a meaningful experience with scholars from around the world. All members of the Congestive Heart Failure 2019 organizing committee looking  forward to meet you in Florence, Italy. 
It’s time to take care of you. So, on behalf of Euroscicon we are glad and privileged to invite you to join the 3rd International Conference onWomen Health and Breast Cancer which is going to be held in Dubai, UAE on September 26-27, 2019. The theme of the conference is aiming to promote quality research and real-world impact in an atmosphere of true international cooperation between scientists by bringing together again the world class researchers, International Communities and Industrial heads to discuss the latest developments and innovations in the fields of Women Health and Breast Cancer. During this conference will have the opportunity to interact with more than 50 world-renowned speakers in the field of women health, sharing the…
3rd International Conference on Women Health & Breast Cancer
This seminar will provide a great resource to Pharmaceutical, Biotechnology, Diagnostics, Cell Therapy, Drugs, Biologics, OTC, Radio-pharmaceutical, Pharmacies and Medical Device Industries in understanding the effective way to establish a new or modified product stability testing program. This program is an important part of a product's regulatory filing requirements as well as the determination of the shelf life or expiration date of the product. This is an important part of every business final bottom line or indirectly relationship to their supply and warehouse chain (how long the product can be stored before it can be discarded). Understanding how to design and implement an effective stability testing program following the regulatory guidelines will allow the product to be manufacture…
Designing and Sustaining New and Existing Product Stability Testing Program