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Events

Amsterdam, Government of Amsterdam, Netherlands

World Biochem 2019  is very glad to invite proficient delegates, scientists, professors, students, young researchers, business executives, scholars, chemists and professionals across the globe to be a part of World Congress on Biochemistry and Enzymology at Amsterdam ,Netherlands in month of March 25,26 2019. Keynote speech, exhibitions, oral and poster presentations outline the key attractions of the conference on the theme "Delve into the chemical concepts of biology”. http://biochemistrycongress.alliedacademies.com/ biochemistry@alliedscholars.com World Congress on Biochemistry and Enzymology +448000868979
25-Mar-2019 - 27-Mar-2019

Venue to be confirmed

Course overview This course is designed for those with at least two years worth of knowledge in drug safety and will provide a comprehensive, yet practical assessment of the main regulations required to produce a compliant reporting company pharmacovigilance Inspection. KEY TOPICS TO BE COVERED Training for Drug Safety Reporting Duties, Audits and Expectations Risk Based Inspections The DDPS retirement and the New PV Master file in the EU Compliance and Drug Safety Product Safety Reviews Purpose and Function (incorporating the new EU Signal Analysis Requirements) Developing Company Core System Information CIOMS III Safety Reporting in Licensing Agreements PSURs Timing, Content and the DSUR and the New ICH E2C (2…

Rome, Metropolitan City of Rome, Italy

8th Edition of International Conference on Internal Medicine & Patient Care, March 25 -26, 2019, Rome, Italy                                                                             Internal Medicine conferences 2019 | Patient Care Congress 2019 | CME Medical Conferences 2019 | Primary Care Meetings 2019     The EuroSciCon is holding its 8th European Congress on Internal Medicine & Pat…

Melbourne, Australia

Dear colleagues and friends, On behalf of the AAC, it’s our great pleasure to welcome you to the Infectious Diseases & Primary Healthcare, which will be held from March 25-26,2019 in Melbourne, Australia. As past meeting was an awesome achievement, the current year's 2019 gathering will draw in participation from all around the globe; the recognized speakers are from the first-class scholarly organizations and additionally driving medicinal services businesses from all around the world. We welcome you all for Healthcare 2019. We would love to meet you and learn more about your professional development pursuits in the world of experiential education. We hope that you will find the conference and your stay in Melbourne both valuable and enjoyable. Since…

11, Thurloe Place, London, Greater London, SW7 2RS, United Kingdom

Course overview Working in the pharmaceutical and device industries has become increasingly challenging and fast moving. Previously, excellence in technical areas would have guaranteed a successful career. Now, to develop and even sustain your career you will almost certainly need to build your leadership skills to perform in your existing role or gain promotion. As companies turn more towards team working – both in departmental and multifunctional teams – to maximise an organisation’s performance, employers are looking for people who can genuinely lead their staff, departments, projects and organisations to success. Leadership skills are an extremely valuable commodity and need to be learned (rarely are they naturally acquired). As a leader you are expected to inspire vision, d…

81, Jermyn Street, London, Greater London, SW1Y 6JF, United Kingdom

Course overview This course will show you how to plan for and undertake the conformity assessment process for your medical device to demonstrate that your product meets the enhanced requirements of the new Medical Devices Regulation (MDR). As with the current Directive, the choice of conformity assessment route depends on the classification of the device. Once you have undergone a valid conformity assessment process and shown that your device has met the new requirements, you will be in a position to place a CE mark on your product which is your access to the European market. This course will provide essential guidance on how to undertake a successful conformity assessment process and subsequently apply (or continue to apply) the CE mark. The importance of quality management syst…

Venue to be confirmed

Course Overview Countries to be covered include: Algeria, Botswana, Ethiopia, Ghana, Kenya, Malawi, Morocco, Mozambique, Nigeria, Namibia, South Africa, Tanzania, Tunisia, Uganda, Zambia, Zimbabwe The aim of this seminar is to provide you with an understanding of the key areas of regulatory affairs in the region, a focus on the practical aspects to assist with regulatory activities. Also the opportunity for you to participate in interactive discussions and exchange experiences with other delegates. Why you should attend Topics to be covered at this meeting Overview of the Regulatory Requirements within African countries Company and product registration Practical information on Compiling Dossiers How to comply with Regulatory Submission Strateg…
27-Mar-2019 - 27-Mar-2019

81, Jermyn Street, London, Greater London, SW1Y 6JF, United Kingdom

Course overview Quality, Quality, Quality: from manufacture, through fill/finish to final inspection This seminar has been designed to provide a comprehensive, practical and usable overview of the production of Pre-Filled Syringes and will provide the latest information on manufacture, packaging for fill/finish through to final (post-fill) inspection. Quality will be a key focus for the day and topics such as quality of syringe manufacture, quality of syringe components and why, quality of filling (volume check, reject reduction), quality of inspection and product release will be discussed in detail. Why should you attend? Gain a comprehensive update of the manufacture of pre-filled syringes from experts in the field Discuss key areas of quality in syringe manufa…

CTC Offices

Highly interactive course with a balance of information, workshops, exercises and quizzes offering a general overview of the drug development process including relevant tasks and responsibilities within the clinical research setting. It provides details on how drugs are developed and who the key players in the process are, about the terminology used in the clinical research environment and what rules, guidelines and laws are essential. How a clinical study is set up and performed and how to handle the documentation required in clinical research.
28-Mar-2019 - 29-Mar-2019

81, Jermyn Street, London, Greater London, SW1Y 6JF, United Kingdom

Conference Overview The pharmaceutical industry and its main markets continue to change. Geopolitical changes influence healthcare industry funding models, demographic changes (in developed countries) increase the demand for healthcare and technology advancement opens up new opportunities. In drug delivery we have witnessed a very significant transition. For many years oral tablets held the leading market positions. For example, at one time oral H2 receptor blockers were the blockbusters. These were replaced by proton pump inhibitors and then cholesterol lowering drugs as the world’s biggest sellers. Today, depending upon which list you look at, around 9 of the world’s 12 best-selling drugs require a drug delivery device, as they are biologics for parental delivery or drugs for treatmen…
28-Mar-2019 - 28-Mar-2019

11, Thurloe Place, London, Greater London, SW7 2RS, United Kingdom

Why you should attend? Risk management is becoming increasingly important to running clinical trials. There are now numerous pharmaceutical guidelines covering risk management including ICH Q9, the revised ICH GCP R2 guideline, the revised EU Clinical Trial Regulation guideline on risk management and several other risk management clinical research standards and initiatives. This essential one day course will explain the importance of using risk management techniques in clinical research to comply with the latest focus on GCP inspection in this area. It will show you how risk management can improve the quality of your clinical trials and demonstrate the importance of using risk analysis and risk management techniques in clinical trials. You will learn how to identify, evaluate and als…

11, Thurloe Place, London, Greater London, SW7 2RS, United Kingdom

Course overview Clinical research is a constantly evolving eld and the regulatory requirements are regularly being updated. In order to stay up to date and maintain your GCP knowledge it is important to receive regular training This course provides an update on recent changes to relevant legislation and guidance and will discuss how these changes have been implemented Topics covered will include ICH GCP R2, the EU Clinical Trial Regulation, Data Integrity and the impact of GDPR on clinical trials. The programme will discuss inspection ndings and common failings in these new areas and how these should be addressed This is a highly interactive course suitable for those who need to update their knowledge and to demonstrate recent and up-to-date trai…

Frankfurt, Darmstadt, Germany

The Organizing Committee takes an immense pleasure in inviting you to the 16th International Congress on “Oncology Nursing and Cancer Care” on April 01-02, 2019 at Frankfurt, Germany  for productive collaborations and an opportunity to present their work in the field of cancer. Cancer Nursing 2019 welcomes all the renowned and aspiring researchers, scientists and business delegates, who are significantly putting their effort to improve the life of population with Cancer. Scientific sessions of Cancer Nursing 2019 will be systematized on the theme “Pioneering Approaches and challenges in the era of Cancer research and Oncology Nursing” To know more details, Visit: http://cancernursing.alliedacademies.com/ To Book your slots, Visit: http://cancernursing.alliedacad…
01-Apr-2019 - 02-Apr-2019

Queen's Lane, Oxford, Oxfordshire, OX1 4AR, United Kingdom

  Twitter: @LPMHealthcare; #OligoOx19 We are delighted to announce our 5th annual Oxford Symposium on antisense and therapeutic oligonucleotides. The symposium is aimed at bringing together chemists and biologists from academia and industry to discuss the latest advances and breakthroughs in the development of synthetic oligonucleotides as therapeutics. The symposium agenda is currently in progress and we welcome proposals for oral and poster presentation on THERAPEUTIC APPLICATIONS AND DELIVERY STRATEGIES of synthetic oligonucleotides, including: >Antisense & catalytic oligonucloetides, aptamers, siRNAs, miRNAs, antagomirs >Chemical modifications >In vitro/in vivo applications >Delivery strategies >New technologies …

Venue to be confirmed

Course overview Whilst licensing agreements involving medicines are primarily driven by commercial considerations, the successful handling of pharmacovigilance obligations is a critical, but frequently overlooked, consideration. Negotiating the safety arrangements to ensure regulatory compliance by both partners can be a complex process. This is further compounded by lack of harmonisation and clarity of the regulations around the world. This seminar will review the existing global requirements relating to pharmacovigilance in contractual agreements. The emphasis will be on practical advice as to how to remain compliant with the legal obligations, how to satisfy good pharmacovigilance practice and quality management requirements, as well as how to promote harmonious business partner…

81, Jermyn Street, London, Greater London, SW1Y 6JF, United Kingdom

Course Overview  This seminar provides an essential overview of medical device clinical evaluations, clinical investigations, post-market clinical follow up requirements and adverse event and vigilance reporting for medical device clinical studies complying with the European Medical Device Directive 93/42/EEC. It will provide a good introduction to medical device clinical studies and serve as an update for those with experience who need to keep abreast of the regulatory changes and the methods of handling adverse events during the study period. By attending this meeting you will: HEAR all you need to know about the regulatory requirements for monitoring and reporting adverse events in one information packed day FIND OUT when a clinical investigation is nee…
03-Apr-2019 - 03-Apr-2019

19, Via Masaccio, Milano, Città Metropolitana di Milano, 20149, Italy

Negli ultimi anni, il numero e la tipologia delle attività relative agli studi clinici che vengono esternalizzate dall’industria farmaceutica sono aumentate notevolmente. Non è pertanto sorprendente che nella ICH E6 (R2) si siano affrontate in modo più dettagliato le aspettative di supervisione di terze parti. L’addendum comporta una serie di modifiche negli accordi contrattuali e nei processi che vedono coinvolti investigatore, sponsor e CRO che consentiranno un’efficace gestione dei rischi di qualità, fondamentale per la protezione dei soggetti umani e l’affidabilità dei risultati degli studi. ICH-GCP sezione 5.2.2 „the sponsor should ensure oversight of any trial-related duties and functions carried out on its behalf.” L’XI° edizione di Italian ePharma Day esplorerà quindi…
03-Apr-2019 - 04-Apr-2019

Cowley Place, Oxford, Oxfordshire, OX4 1DY, United Kingdom

Twitter: @AptamerSociety | @JAptamers | #AptaOx19 Email: AptamersOxford@gmail.com Our 6th Oxford meeting – Aptamers 2019 – will address therapeutic, diagnostic, analytical and basic research applications of aptamers and invites oral and poster abstracts from academic and industrial researchers. We particularly encourage final year doctoral students and early/mid career postdoctoral researchers/junior group leaders to submit oral abstracts, as we believe this event will provide their research excellent exposure, critical analysis by attending senior researchers and new career opportunities. The symposium will feature: >High-impact talks, discussions & several hours of networking >Oral presentations by an i…
03-Apr-2019 - 03-Apr-2019

CTC Offices

The course offers a general overview of the drug development process and most relevant tasks and responsibilities within the clinical research setting It provides details on how drugs are developed and who the key players in the process are, about the terminology used in the clinical research environment and what rules, guidelines and laws are essential. How a clinical study is set up and performed and how to handle the documentation required in clinical research.
04-Apr-2019 - 05-Apr-2019

Venue to be confirmed

The programme will cover the regulatory landscape, the definition and classification of ATMPs and provide practical guidance on how to overcome quality and specific GMP challenges. Comparison of the differences between GMP for Advance Medicinal Therapeutic Product (ATMPs) and conventional therapeutics will be discussed. Consideration of what is required for clinical trials and the preparation of the IMPD will also be addressed. Furthermore advice on the specific transportation requirements of these products will be included. This seminar will be of benefit to all those involved with or considering developing an Advance Medicinal Therapeutic Product.