World Conference Calendar

31707 Conferences

Physical and Life Sciencesrss


INTRINSICALLY DISORDERED PROTEINS IN BIOMEDICINE

INTRINSICALLY DISORDERED PROTEINS IN BIOMEDICINE

Location: , Spain
Category: Physical and Life Sciences
Start Date: 10-04-2010 Last Day: 10-06-2010 Deadline for abstracts: 07-15-2010
Intrinsically disordered proteins are Nature’s response to the increased complexity of higher organisms and are associated with diseases such as Cancer and Neurodegeneration. Genome sequencing projects and bioinformatics analyses have shown that disordered proteins are highly abundant in eukaryotes and are tightly regulated. Enabling technologies that offer structural information in solution, such as Nuclear Magnetic Resonance, Small Angle X-ray scattering, and single molecule fluorescence, are providing novel insights into the structural propensities and interactions of disordered proteins. A new paradigm, in which dynamic averaging of conformational ensembles is central, is emerging for the structural and functional analysis of disordered proteins.…
How to conduct a software risk assessment that is meaningful

How to conduct a software risk assessment that is meaningful

Location: , United States
Category: Physical and Life Sciences
Start Date: 10-04-2010 Last Day: 10-04-2010
Get detailed understanding of how to perform risk assessment as part of 10 step risk based approach to CSV. Areas Covered in the Seminar: . How to use the risk-based approach to reduce validation time and lower costs. . Step-by-step instructions for performing and documenting a risk assessment, and how to use the results to reduce validation documentation. . Reduce testing by writing test cases that trace to elements of risk management. . Avoid 483s and Warning Letters. . Interactive real life examples. . How to identify risk and establish mitigations. . Determine risk in a process to reduce the…
Best Practices for Writing an Effective SOP to Lead to Successful FDA Inspections

Best Practices for Writing an Effective SOP to Lead to Successful FDA Inspections

Location: , United States
Category: Physical and Life Sciences
Start Date: 10-07-2010 Last Day: 10-07-2010
This SOP best practices webinar will show how to create “state of the art” SOP or review your current SOP so as to successfully manage FDA Investigators and other Regulatory Authorities Audits which can help improve and influence Audit Outcomes. Areas Covered in the Seminar: Prepare a proactive SOP for Managing a FDA Inspection. Identify clearly roles and responsibilities. Define inspectional policies. Identify key ground rules. Define the Conduct of the Inspection. Handling Introduction -FDA 482. Handling Sampling Request -FDA 484. Handling the End of Inspection -FDA 483. For More Details: http://bit.ly/dBTSfu
What exactly is required for 21 CFR Part 11 compliance?

What exactly is required for 21 CFR Part 11 compliance?

Location: , United States
Category: Physical and Life Sciences
Start Date: 10-08-2010 Last Day: 10-08-2010
This 21 CFR Part 11 compliance training will guide you through the concept of part 11 and explanation of its 3 primary areas SOPs, Product features and Validation (10 step risk based approach). Areas Covered in the Seminar: Which data and systems are subject to Part 11. What Part 11 means to you, not just what it says in the regulation. Avoid 483 and Warning Letters. Explore the three primary areas of Part 11 compliance: SOPs, software product features, and validation documentation. Ensure data integrity, security, and protect intellectual property. Understand the current computer system industry standards for security, data…
Hydrology Conference 2010

Hydrology Conference 2010

Location: , United States
Category: Physical and Life Sciences
Start Date: 10-11-2010 Last Day: 10-13-2010
This major international conference, taking place in San Diego, USA, October 11 – 13, 2010, will target the developing interdisciplinary science themes in the interface between hydrology and other scientific disciplines, including climate change, biology, chemistry and social sciences. These subjects are of particular relevance as population increases and a changing climate bring new pressures on hydrological systems around the world.
How to Investigate Water System Contamination with Example Case Studies

How to Investigate Water System Contamination with Example Case Studies

Location: , United States
Category: Physical and Life Sciences
Start Date: 10-15-2010 Last Day: 10-15-2010
In this Water System Webinar the author will explain the process he uses as a consultant for investigating and solving water system or product contamination problems with water organisms. Case studies of real life problems he has resolved will be presented to illustrate the process. Though there is no rule book or SOP for such contamination problem solving, learn the best practices of solving these problems from an expert. Areas Covered in the Seminar: - Early information; gathering and assessing user opinions. - Investigation approach elements-- the various rocks to be turned over. - Five water system/product contamination case studies.…
The Tougher U.S. FDA - One Year Later

The Tougher U.S. FDA - One Year Later

Location: , United States
Category: Physical and Life Sciences
Start Date: 10-19-2010 Last Day: 10-19-2010
This FDA compliance webinar will evaluate the FDA expectations in the near term and further out in the future and how it will boil down to new regulatory climate. Areas Covered in the Seminar: * Stated expectations and the one-year result. Targets. * Avoid complacency from past "good" FDA actions. * Avoid complacency from just completed "good" ISO feedback. * FDA's desired responses from industry. * How to respond now -- where to shift focus first. * Where to direct scarce resources. * Anticipated future directions. * Maintain 'the edge'. Who Will Benefit: This webinar will provide valuable assistance to…
5th Annual Generics Asia Summit

5th Annual Generics Asia Summit

Location: , Singapore
Category: Physical and Life Sciences
Start Date: 10-25-2010 Last Day: 10-26-2010
The 5th Annual Generics Asia Summit will bring together C-level decision makers from Generics companies, innovator pharma companies, payers, investors, regulators and health authorities to discuss business strategy and to form partnerships in an evolving industry landscape. This is the only event in Asia to have truly substantial and relevant discussions on the hottest issues such as leveraging on brands, biosimilars, regulatory updates and collaboration opportunities between innovator pharma and traditional generics companies. Whether you have or plan to invest in the regulated, semi-regulated or unregulated markets , this event will provide you with actual case studies on how to…
Full Day Virtual Seminar - Design and Validation of Excel Spreadsheets: Step-by-Step

Full Day Virtual Seminar - Design and Validation of Excel Spreadsheets: Step-by-Step

Location: , United States
Category: Physical and Life Sciences
Start Date: 10-26-2010 Last Day: 10-26-2010
In this excel Spreadsheet validation full day webinar training, learn the best way to design and validate the excel spreadsheets. Learn what the requirements are of excel validation and how to implement it to comply with regulations. Why Should You Attend: Excel spreadsheets used in regulated environments should be validated and comply with other FDA requirements. In this interactive one-day on-line seminar Dr. Ludwig Huber will give an introduction to FDA, GAMP® 5 and other requirements for validation of excel sheet and present approaches for implementation. This is a comprehensive course covering validation, design, testing of functions along with how…
Drug Safety Assessment and Risk Minimization in the Development Period - Webinar By ComplianceOnline

Drug Safety Assessment and Risk Minimization in the Development Period - Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 10-26-2010
This drug safety training will discuss the various factors to be considered and the principles of risk assessment to be followed during drug development to minimize risk. Areas Covered in the Seminar: Risk conceptualization. Goals of project risk management. Risk management planning & safety review teams. Intellectual property. Pharmacovigilance planning in product risk management. Unexpected study results: efficacy, dosage, adverse events & toxicology. Data analysis, interpretation and presentation. Essentials of Data Monitoring Committees. Drug disposal and environmental impact. Labeling as a hallmark of risk management efforts. Post-marketing risk. Who Will Benefit: The Webinar will present valuable risk management information and…
Excel Spreadsheets - Develop and Validate to Eliminate 483s

Excel Spreadsheets - Develop and Validate to Eliminate 483s

Location: , United States
Category: Physical and Life Sciences
Start Date: 11-05-2010 Last Day: 11-05-2010
Learn how to Use excel spreadsheet for GXP data and reduce validation cost and time. Configure Excel for audit trails, security features, and data entry verification. Areas Covered in the Seminar: . Become compliance when using Excel spreadsheets for GxP data. . Reduce validation time and costs. . Increase compliance while lowering resource needs. . Avoid 483s and Warning Letters. . Understand what validation documentation is required. . How to use Excel’s audit trail. . Hands on workshop to address your specific needs. . How to use cell and file protections. For More Details: http://bit.ly/dqBloH
Performing Investigations for Environmental Excursions - Webinar By ComplianceOnline

Performing Investigations for Environmental Excursions - Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 11-18-2010
This Webinar will discuss the modalities of proper investigations for environmental excursions and how to find the root cause and take appropriate preventive actions. Areas Covered in the Seminar: Why investigate environmental excursions. Identifying an excursion - now what do I do? Compling all necessary information. Analzying information (including trend analysis). Driving to root cause. Defining appropriate corrective actions. Evaluating effectiveness of corrective actions. Who Will Benefit: This webinar will provide valuable assistance to regulated manufacturing and laboratories that support microbial testing. Microbiologists Quality Control personnel Environmental Monitoring personnel Quality Assurance
Important requirements when validating sterilizing grade filters - Biotechnology Webinar By ComplianceOnline

Important requirements when validating sterilizing grade filters - Biotechnology Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 12-02-2010 Last Day: 12-02-2010
This sterilizing grade filter validation training will provide valuable assistance in validating sterilizing grade liquid filters within the pharmaceutical and biotech processes. Areas Covered in the Seminar: What is filter qualification, what is filter validation. Regulatory requiremnents validating sterilzing grade filters. Various validation requirements and processes. Practical experiences with filter validation. Documents required. Who Will Benefit: This webinar will provide valuable assistance to all regulated companies that need to validate their sterilizing grade liquid filters within the pharmaceutical and biotech processes. The employees who will benefit include: End-users of sterilizing grade filters Validation manager or specialists Regulatory manager or support…
National Conference on Nanomaterials - NCN-2010

National Conference on Nanomaterials - NCN-2010

Location: , India
Category: Physical and Life Sciences
Start Date: 12-03-2010 Last Day: 12-04-2010 Deadline for abstracts: 10-07-2010
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 MAJOR TOPICS Nanomaterials including Nanoparticles, Nanocrystals , Nano-porous materials, 2 Nanomechanics, Nanotribology, Nanocomposites, Nanoelectronics, Nano-Magnetics, & Quantum Computing, Nanobiotechnology , Nanomedicine, Nanotubes/Nanowires/Quantum Dots, NEMs, MEMs, Nano-Fluidics, Nano-Actuators, Nano-Sensors, Nano-robotics, 7 Nano-Fabrication, Nano-Lithography, Nanotechnology for Energy (fuel cell, solar cell, hydrogen storage), Other related topics CALL FOR PAPERS The organizing committee invites original research papers for Oral/Poster presentation. Authors are requested to submit an abstract of their work in about…
Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Clinical Compliance Webinar By ComplianceOnline

Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - Clinical Compliance Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 12-03-2010 Last Day: 12-03-2010
In this Clinical Trial Audits training learn the risk management and best practices of GCP audit by reviewing and analyzing recent GCP audit finding from Clinical Investigators (Sites), Sponsors, and Institutional Review Boards (IRBs). Why Should You Attend: Quality assurance is defined as a “systematic and independent examination of trial-related activities and documents” that allows an auditor to determine whether or not the clinical trial was conducted according to the regulations and guidance that govern clinical research. This course will provide an overview of auditing skills and techniques and a review of recent GCP audit findings from Clinical Investigators (Sites),…
4th International Conference on Water Resources and Arid Environments (2010)

4th International Conference on Water Resources and Arid Environments (2010)

Location: , Saudi Arabia
Category: Physical and Life Sciences
Start Date: 12-05-2010 Last Day: 12-07-2010 Deadline for abstracts: 10-30-2009
This bi-annual conference brings together scholars and experts from around the world to share water-related research and is held concurrently with the awards ceremony for the Prince Sultan Bin Abdulaziz International Prize for Water. Conference Objectives: *To provide a scientific framework for awarding the Prince Sultan Bin Abdulaziz International Prize for Water, and for announcing the topics of research for the 5th award. *To exchange knowledge and share information in water resources and desert-related fields. *To explore the use of new technologies in the study of arid and semi-arid environments and their natural resources. *To provide an opportunity for decision…
Evolving Regulatory expectation for Particulates in Biologics - Biotechnology Webinar By ComplianceOnline

Evolving Regulatory expectation for Particulates in Biologics - Biotechnology Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 12-09-2010 Last Day: 12-09-2010
This webinar addresses evolving regulatory requirements for particulates and the techniques suitable for testing and characterizing sub-visible particulates in therapeutic formulations. Areas Covered in the Seminar: Current Regulatory requirements for testing particulates in protein Therapeutics. The limitations of the USP methods for testing Particulates. What are the methods available for analysis of subvisible particles in protein therapeutics? Comparison of size ranges, sensitivity limits and capabilities of the various methods. Equipment available for performing these tests. Advantages and disadvantages of the methods. Who Will Benefit: This course will benefit all individuals involved in Formulating or Testing Protein Therapeutics QC Supervisors and…
Practical Strategies to a successful 505(b)(2) product - Pharmaceutical Webinar By ComplianceOnline

Practical Strategies to a successful 505(b)(2) product - Pharmaceutical Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 12-10-2010 Last Day: 12-10-2010
In this 505(b)(2) related webinar, know the complete details, key strategies, regulatory considerations, and marketing strategies for developing 505(b)(2) products. Areas Covered in the Seminar: The 505(B)(2) regulation and guidance from the FDA. Strategic considerations before embarking on a 505(b)(2) development project. Intellectual property issues with such products. Key development steps for such products. FDA’s review process and ongoing consultation. Challenges to developing 505(b)(2) product and possible solutions. Examples of successful strategies for developing such products. Searching for a 505(b)(2) project, future trends. 505(b)(2) and biosimilars.
How to Set up Data Monitoring Committees (DMCs / DSMBs) and what is effect on the Drug Development Process - Clinical Compliance Webinar By ComplianceOnline

How to Set up Data Monitoring Committees (DMCs / DSMBs) and what is effect on the Drug Development Process - Clinical Compliance Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 12-14-2010 Last Day: 12-14-2010
This Data Monitoring Committees (DMC) webinar will guide you through the essential elements of data monitoring committees and how to set up for it successfully. Areas Covered in the Seminar: The historical background of why Data and Safety monitoring is essential. The purpose of the Data and Safety monitoring plan. The Regulatory requirements for safety monitoring. Studies requiring a formal Safety Monitoring Committees. What does the "Charter" of a DMC compose of? What is the composition and function of a DMC? What types of studies "require" a DMC? Conflict of interest and the DMC. Who Will Benefit: This Webinar will…
Avoiding FDA 483 Observations by Identifying the Root Cause of Deviations - FDA Webinar By ComplianceOnline

Avoiding FDA 483 Observations by Identifying the Root Cause of Deviations - FDA Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 12-17-2010
This webinar addresses the adequate investigation of deviations, an area that is receiving FDA attention as evidenced by citations in Warning Letters and 483 observations. This course will include a discussion of the Deviation System, what should be investigated and the level of investigation. Several tools that will lead to the identification of the root cause will be discussed. These include: process mapping, brainstorming, cause analysis, cause and effect and the 5 Whys. The investigation system will be integrated with the CAPA and Change Control Systems. Areas Covered in the Seminar: What should be investigated - Complaints, audit observations, deviations,…

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