Physical and Life Sciences

In this webinar attendees will learn the key issues and sample requirements (collection methods, sample inhibition and sample volume) for molecular diagnostics and the tools (PCR, DNA fluorescent assays & NGS assays) you need to deal with your laboratories challenges in clinical laboratory.

This Workshop is one of a series of workshops planned at selected international sites to familiarise and discuss implementation issues with key users with the 2018 SPE/WPC/AAPG/SPEE/SEG/SPWLA/EAGE Petroleum Resource Management System (PRMS). Consisting of two days of informal sessions, including a number of presentations and discussions per session, participants are encouraged to contact the Organizing Committee with potential subjects they would like to present. By attending an SPE workshop, you can network with knowledgeable industry experts who are enthusiastic about discussing and advancing technology and best practices. Staged in an intimate setting, an SPE workshop brings together EandP professionals with…

Many Quality Engineers join the workforce with technical understanding of the products without the statistical understanding of product variability. The FDA's findings of deficiencies concerning sample size, gage studies, statistical process control and other statistical issue indicate the agencies expect definitive evidence that statistics are properly applied. Case studies and example from FDA 483 findings will be presented. The cost of non-compliance is therefore more than that of compliance. Are you in compliance with the FDA regulations? In this two day workshop conference you will learn the different statistical tools necessary to comply with global agencies expectations. Through case study…

Big point: Prof. Hartmut Hinz, University of Applied Sciences, Frankfurt, Germany will be our conference chair. All the accepted papers will be published into International Conference Proceedings, which is indexed by EI Compendex, Scopus, Thomson Reuters (WoS), Inspec,et al. One day tour == Submission Methods: Email: [email protected] http://confsys.iconf.org/submission/iccge2019 (.pdf only)

ICESD 2019 Shining Points: 1. Accepted and published papers can be published into international conference proceeding which is indexed by EI Compendex, Scopus, Thomson Reuters (WoS), Inspec,et al. 2. Two Outstanding Professors have joined as Speakers. They are Prof. Miklas Scholz from Faculty of Engineering, Lund University, Sweden;Prof. Khalil Hanna, Graduate Engineering School of Chemistry of Rennes, France 3. The ICESD 2018 was very successfully held in Paris, France and we had one day tour to Paris. ++ Paper Publishing ICESD 2019 papers will be published in international conference proceeding which is indexed by EI Compendex, Scopus, Thomson Reuters (WoS),…

This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintaining computer systems in regulated environments. It details the requirements for Part 11 and Annex 11: SOPs, software product features, infrastructure qualification, and validation. The instructor addresses the latest computer system industry standards for data security, data transfer, audit trails, electronic records and signatures, software validation, and computer system validation. Understand the specific requirements associated with local and SaaS/cloud hosting solutions. It details the requirements for HIPAA Protect Health Information (PHI) Nearly every computerized system used in…

The aim of the Conference: When man discovered Fire his life got brighter when he discovered Wheel his life started to move forward when he found Electricity his life started to faster when he introduced Computer almost entire world is closer our hand, This is the Platform for the Scientist for Innovation for Next Generation in this series is going to Dominate in the world, who knows what might your research as well,

This Computer System Validation Training course will explore proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. Today, the FDA performs both GxP and Part 11 inspections, the Europeans have released an updated Annex 11 regulation that expands Part 11 requirements and companies must update their systems and processes to maintain compliance. Many companies outsource IT resources and are involved in Software as a Service (SaaS) and cloud computing. These vendors are not regulated, and therefore, regulated companies must ensure compliance for both infrastructure qualification and computer system validation to avoid FDA form…

This 2 day seminar will go into the specifics of the REACH and RoHS regulations, provide case studies and share lessons learned so your organization can benefit from the mistakes of others. We will review the latest on both directives and will draw out key developments and key dates (if applicable) with particular emphasis on requirements for US firms. REACH and RoHS have been referred to as "…one of the most complex regulations in the history of the EU." Do not miss this 2 day seminar to find out why. Learning Objectives: After completing this seminar, you will gain a…

Reliable analytical results are necessary to make informed decision about the quality and safety of the products in the pharmaceutical industry. In addition, such analytical data are required for regulatory submissions in support of the drug product registrations. Therefore, meaningful experimental designs including system suitability parameters must be planned for the intended use of the procedure. In this course, general guideline for the determination of the analytical characteristics for different types of validation procedures is highlighted for the analysis of both the drug substance and drug product. The factors to consider for verification of the compendial procedures will also be…

Global Medical Device Regulations continue to evolve, as devices become more diverse and sophisticated. Understanding the regulations and requirements in your targeted markets will expedite speed-to-market of innovative products and assist patients needing access to life-saving products and technologies. Government Regulatory Authorities, needing to become more efficient with their time, are looking for ways to better use their internal resources without compromising safety in products, which become marketable. One such example is the Medical Device Single Audit Program [MDSAP], where Authorized Organizations would be allowed to carry out a single GMP audit on medical device manufacturing facilities and have it…

Optimise HCP-Focused, Patient-Centric Digital Strategies Compliantly With New Tech Trends, Innovative Social & Savvy Integrated Campaigns For Engaging, Customer-Centric, Multi-Channel Digital Pharma Marketing Strategies Monetise Data & Customer Insights, Transform Cultures, Embed Digital Innovation, Prove ROI, Empower The Sales-Force & Deliver Results – Get Inspired By Today’s Digital Disruptors & Innovators at our One-Day Brand-Led Conference & Networking Event, taking place at One Great George Street, Central London. 37 brands speaking including: Pfizer, GSK, Sanofi, Bristol-Myers Squibb, LEO Pharma, BNP Paribas and many more!

2nd International Conference on Inventive Research in Material Science and Technology (ICIRMCT 2019) is being organized on 30-31 January, 2019 by the RVS Technical Campus, Coimbatore, India.

The aim objective of 11th CEBU – Philippines International Conference on Environmental, Chemical, Biological and Medical Sciences (ECBMS-19) is to provide a platform for researchers, engineers, academicians as well as industrial Professionals from all over the world to present their research results and development activities in Environmental, Chemical, Biological and Medical Sciences. The conference will be held in Cebu (Philippines) During Jan. 29-30, 2019.

Come to learn: How subsidy free projects are currently being funded and developed across Spain, UK, Portugal and Italy What Oil and Gas companies and utilities are planning in the clean energy finance space What are the prices manufacturers will be able to achieve without MIP How developers are making subsidy free projects work through numerous case studies The state of the secondary market and the refinancing deal flow Come to meet: All the top European asset owners looking to expand their portfolios, maximise ROI and invest abroad All the top European developers active in the subsidy-free space All the…

Publication & Indexing IOP Conference Series: Earth and Environmental Science (EES) indexed by Ei Compendex and Scopus History: ICEES 2017 | Thammasat University, Thailand | January 22-24, 2017 ICEES 2018 | University of Malaya, Malaysia | January 16-18, 2018 Keynote Speakers: 1-Prof.Chul H. Jo,Inha University, South Korea; 2-Prof. Saad Mekhilef (IET Fellow),University of Malaya, Malaysia.

 Keynote Speakers: * Prof.Chul H. Jo Inha University, South Korea * Prof. Dr. Saad Mekhilef University of Malaya, Malaysia  Publication: * All the accepted papers of ICRET 2019 (After proper registration and presentation) will be collected in the conference proceedings, which will be as a volume of IOP Conference Series: Earth and Environmental Science (EES). * Conference Proceedings Citation Index – Science (CPCI-S), (Thomson Reuters, Web of Science), Scopus, Ei Compendex, etc.  Submission: 1. Log in the Electronic Submission System (http://www.easychair.org/conferences/?conf=icret2019) and submit your paper; 2. Any questions about submission, please contact [email protected].

The objective of this Conference is to bring together researchers from both academia and industry under one roof, to discuss and to share the latest developments in the field of nanotechnology and other advanced research areas. MAJOR TOPICS OF THE CONFERENCE INCLUDES Nanomaterials including Nanoparticles, Nanocrystals, Nano-porous materials, Nanotribology, Nanocomposites, Nanoelectronics, Nano-Magnetics, Nanobiotechnology, Nanomedicine, Nanotubes/Nanowires/Quantum Dots, NEMs, MEMs, Nano-Fluidics, Nano-Sensors, Nano-robotics, Nano-Fabrication, Nano-Lithography, Nanotechnology for Energy (Fuel cell, Solar cell, Hydrogen storage), Other research areas, Crystal Growth , Thin films, Ultrasonics, solid State Ionics The organizing committee invites original research papers for Oral/Poster presentation. Authors are requested to submit an…

It’s our great pleasure to welcome you all for the International Conference on Optics, Photonics and Lasers scheduled during January 24-25, 2019 at Bangkok, Thailand. Laser Technology not just make a phase to exchange estimations to the enormous social occasion of individuals, yet also endeavour to spread concentrated and research advances in the clinical, definite and physiological parts of medicinal and designing. We hope that you will grasp this academic occasion to revitalize the enduring connections and flash with new peers around the globe. The theme of Optics, Photonics and Lasers Conference 2019 is “Explore the Possibilities with an Exceeding…

This China & Pacific Rim life science compliance-based seminar will discuss the regulatory structure and requirements for compliance with in-country regulations for Pharmaceuticals, Medical Devices, Biologics and Combination Products. China has been improving its regulatory regime governing the food and pharmaceutical industry in recent years. In 2010, by promulgating the amended GMP and amending GLP, GCP, GSP and other regulations, China will further align the country with international standards of practice. For manufacturers and distributors of drugs and medical devices in China, it is important to pay close attention to the pace at which SFDA implements these changes and to…