- Global Pharma News & Resources


25-Mar-2019 - 26-Mar-2019

3600, Sansom Street, Philadelphia, Philadelphia County, 19104, United States

With pharmaceutical and medical device companies receiving thousands and thousands of product complaints and potential recalls each year, it's essential that they follow FDA requirements. By having an effective complaint management system, life science organizations have a better chance to ward off inspections by using the appropriate guidelines and regulations. Monitoring complaint trends over time and having a complaint program improves the customer's experience with your products. The 3rd Product Complaints Forum will expand on last year's conference by providing current trends, best practices, and strategies to reduce product complaints and avoid inspections. Come network and learn from over 65 industry experts and choose between two tracks on Day Two that explore specific industry ch…

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 & Patient Care…

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, devel…

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 systems, ri…

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.

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: To Book your slots, Visit:…
02-Apr-2019 - 05-Apr-2019

1, Messeplatz, Wien, 1021, Austria

Accelerate your biologics, mAbs, vaccines and novel products towards commercial success by attending BioProcess International Europe, held 2-5 April 2019 in Vienna, Austria. NOVEL SCIENCE - Your registration fee includes access to 120+ live case study and new data presentations across 7 streams focused in upstream, downstream, continuous manufacturing, industry 4.0, vaccines, cell line development, and viral safety /raw materials. INNOVATIVE TECHNOLOGY - Meet 120+ global CROs, CMOs and suppliers that cater exclusively to the biopharmaceutical production market.  View live product demonstrations and stay at the forefront of bioprocess innovation. UNPARALLELED NETWORKING - Connect with 900+ global bioprocessing scientists and decision makers during networking luncheons and cocktail r…

Amsterdam, Government of Amsterdam, Netherlands

2nd InternationalConference & Expo on Clinical Psychology, in short, Clinical Psychology 2019 is accredited with CME and CPD credits and organized with the theme of "Together towards the betterment of Mental Health and Well-Being" is scheduled on April 03-04, 2019 at Amsterdam, Netherlands.   Conference Highlights Following are the lists of conference major topic which will be discussed in the Clinical Psychology Conference 2019   Clinical Psychology | Cognitive Behavioral Therapy | Mental Health | Behavioral Psychology | Clinical Neuropsychology | Psychological Disorders | Factors Affecting Psychological Disorders | Humanistic Psychology | Child and Adolesc…
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 i mol…
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.

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

Course overview New for 2019 The ISO 10993 series of standards covering biological evaluation of medical devices is well established and regulatory authorities worldwide expect compliance. In Europe compliance with the standards will be the easiest way to meet the relevant essential product safety requirements of the Medical Device Regulation. Understanding a risk management approach to biological evaluation is essential. This seminar will provide key guidance on how to use the standards and successfully apply a risk management approach to the biological evaluation of medical devices. There will be plenty of time for interactive discussion with experts in this field. Who should attend? This seminar will be of importance to those in the medical device industry from the f…

41, Münchensteinerstrasse, Basel, Basel-Stadt, 4052, Switzerland

This workshop is designed to provide a solid foundation of Pharmacovigilance (PV) in Clinical Trials. It will introduce the most important terms and definitions, MedDRA (Medical Dictionary for Regulatory Activities) coding, SAE (Serious Adverse Event) management, unblinding processes, SUSAR (Suspected Unexpected Serious Adverse Reaction) submission, and a first glance at a PV database.

41, Münchensteinerstrasse, Basel, Basel-Stadt, 4052, Switzerland

The purpose of this workshop is to introduce Pharmacovigilance (PV) in Post Authorisation. It will provide essential background knowledge on the origin of PV, sources for cases, case assessments in post authorisation, special situations, quality complaints, and case submissions

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

Why you should attend The new EU Clinical Trial Regulation (536/2014) will replace the European Clinical Trials Directive (2001/20/EC). The new regulation was originally due to come into effect in 2016, however implementation has been delayed until the new portal and clinical trial database have been completed and audited. Key aims of the new regulation are to harmonise procedures for carrying out clinical trials across the EU and to simplify the clinical trial approval dossier by submission through a new clinical trial database and portal. Guidelines for enacting the new regulation are also being prepared in a number of areas including inspection, investigational medicinal product and trial documentation etc. This course will provide an essential understanding to help with compliance wi…
11-Apr-2019 - 12-Apr-2019

Holiday Inn London - Kensington Forum, 97 Cromwell Road, London, London, SW7 4DN, United Kingdom

This conference gives a comprehensive review within the field of nasal drug delivery while reviewing the very latest new data and innovative technologies.
23-Apr-2019 - 23-Apr-2019

York, York, YO10 5DD, United Kingdom

This training day focusses on the development of economic models specifically in the area of oncology. The sessions will include overviews of the most common methods for modelling treatments for cancer, and will pay particular attention to the areas that prove most challenging in HTA, including survival curve analysis, data extrapolation, quality of life modelling (including adverse events), handling treatment discontinuation, modelling disease progression and post-progression model assumptions. The day will draw on examples from previous HTA submissions and will provide a number of recommendations for modelling frameworks. This course will be particularly suited to those people that commission oncology models. Please note that other more ‘hands-on’ modelling courses are run by the Univers…

The Rembrandt Hotel, The Rembrandt Hotel, 11 Thurloe Place, London, London, SW7 2RS, United Kingdom

This seminar will provide an overview of the key areas of pharmaceutical regulatory affairs in Asia including, China, Hong Kong SAR, Brunei, the Philippines, India, Indonesia, Malaysia, Singapore, Thailand, Cambodia, Laos, Vietnam, Taiwan, Korea, Japan

3500, Cessna Drive, Richmond, Greater Vancouver, V7B 1C7, Canada

18th International Conference on Industrial Chemistry and Water Treatment aims to provide an up-to-date source of information on a variety of selected topics. The conference will be organized on the theme of Sustainable Industrial Chemistry & Advanced Measures for Waste Water Treatment: Improving Existing Technologies, this conference is going to be held from April 26-27, 2019 in Vancouver, Canada. International Conference on Chemistry and Water Treatment will offer an exciting, & wide range of scientific programme designed to engage high profile scientific international on topics of importance related to the Industrial Chemistry and Water Treatment. This Conference will be the perfect occasion for the international and Indian experts to share their leading-edge knowledge on innova…
29-Apr-2019 - 29-Apr-2019

41, Münchensteinerstrasse, Basel, Basel-Stadt, 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. These days, clinical efficacy alone is not enough; both clinical effectiveness and 'value for money' are essential to make sure the product reaches the patients for whom it is intended. Course Topics Introduction to Market Access Landscape: Who are the Stakeholders and what are ytheir perspectives Health Outcome Assessment types Pricing Country systems

11, The Rembrandt Hotel, 10-12 Rivington Street,, London, Choose One, EC2A 3DU, United Kingdom

One-day intensive briefing on best practice and employment law requirements for the effective HR assistant