World Conference Calendar

33841 Conferences

Physical and Life Sciencesrss


Hydrobiology and Ichthyology of biological invasions in freshwater ecosystems

Hydrobiology and Ichthyology of biological invasions in freshwater ecosystems

Location: , Russia
Category: Physical and Life Sciences
Start Date: 11-22-2011 Last Day: 11-25-2011 Deadline for abstracts: 10-24-2011
Topics / Symposia: Biodiversity in freshwater ecosystems The diversity and composition of alien species in freshwater ecosystems Ways and mechanisms of bioinvasion Interaction of alien and native species The influence of alien species on biological productivity of freshwater ecosystems Biomonitoring of bioinvasion The use of invasive species in the assessment of water quality and ecological status of reservoir The conference is completely virtual, you can experience it from the comfort of your own desk. Save yourself time and the travel expenses Our conference is not a typical web seminar. it is an interactive event in 3D virtual space that incorporates…
2nd World congress on Biotechnology-2011

2nd World congress on Biotechnology-2011

Location: , United States
Category: Physical and Life Sciences
Start Date: 11-29-2011 Last Day: 12-01-2011 Deadline for abstracts: 08-29-2011
OMICS Group, the World class Open Access Publisher and Scientific Events Organizer hosting 2nd World Congress on Biotechnology during 29 Nov – 01 Dec 2011 Philadelphia, USA Biotechnology-2011 will serve as a catalyst for the advances in the field of Biotechnology by connecting scientists within and across disciplines at sessions and exhibition held at the venue, creates an environment conducive to information exchange, generation of new ideas, and acceleration of applications that benefit Research in Biotechnology.
The 2011 International Conference on Biomedical Sciences, Life Sciences & Innovative Medicine [BIOTEC 2011]

The 2011 International Conference on Biomedical Sciences, Life Sciences & Innovative Medicine [BIOTEC 2011]

Location: , India
Category: Physical and Life Sciences
Start Date: 12-01-2011 Last Day: 12-04-2011
The 2011 International Conference on Biomedical Sciences, Life Sciences & Innovative Medicine [BIOTEC 2011]is a truly international forum on research, development and application of Innovative Medicine, Life Sciences and Biomedical Sciences. BIOTEC'11 aims to facilitate debate on topics from a whopping range of Biomedical related areas of research. This is one field that needs constant innovation and drug discovery to improve the lifespan and health of mankind. This event will enable dynamic networks among academia, industry and government which will innitiate collaborative research on a global scale. On behalf of our multinational sponsor Aries Group and our collaborating partners, we…
ABC’s in Equipment Qualification - Webinar By ComplianceOnline

ABC’s in Equipment Qualification - Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 12-14-2011 Last Day: 12-14-2011
Why Should You Attend: This training will show how you can plan and execute an equipment qualification project, whether it is retrospective qualification (all the equipments are in place and the production lines are working), or prospective qualification (carried out after the installation and commissioning of a brand new equipment). The session will cover a Validation Master Plan (VMP), Installation Qualification (IQ) basics, Operational Qualification (OQ) basics, and everything about Performance Qualification (PQ), where we will illustrate the performance testing measures and the correlation between Performance Qualification and Process Validation. The training will give attendees a road map to plan,…
Dietary Supplements: Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA Updates

Dietary Supplements: Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA Updates

Location: , United States
Category: Physical and Life Sciences
Start Date: 12-14-2011 Last Day: 12-14-2011
Why Should You Attend: The FDA, with assistance from the FTC, has become increasingly aware of the large amount of dietary supplements that have come onto the market since the passage of the Dietary Supplement Health and Education Act in 1994. A growing public demand for supplements, along with a relatively relaxed pre-market approval process, has resulted in a flurry of companies creating and marketing their own dietary supplements in the United States. With FDA beginning to take a stronger stance on Dietary Supplement enforcement, it is important for companies to verify that their products comply with the latest regulations…
International Conference on Chemical, Biological and Environment Sciences (ICCEBS'2011)

International Conference on Chemical, Biological and Environment Sciences (ICCEBS'2011)

Location: , Thailand
Category: Physical and Life Sciences
Start Date: 12-23-2011 Last Day: 12-24-2011 Deadline for abstracts: 10-25-2011
2011 International Conference on Chemical, Biological and Environment Sciences (ICCEBS’2011) is the premier forum for the presentation of new advances and research results in the fields of theoretical, experimental, and applied Chemical, Biological and Environment Sciences Applications. The conference is mainly managed, promoted and sponsored by Planetary Scientific Research Centre. The conference will bring together leading researchers, engineers and scientists in the domain of interest from around the world. Topics of interest for submission include, but are not limited to: Air pollution and its effects on ecosystems Brain Science and Education Coasts and Seas Cognitive Neuroscience of Memory and Cognition…
International Conference on Ecological, Environmental and Biological Sciences (ICEEBS'2012)

International Conference on Ecological, Environmental and Biological Sciences (ICEEBS'2012)

Location: , United Arab Emirates
Category: Physical and Life Sciences
Start Date: 01-07-2012 Last Day: 01-08-2012 Deadline for abstracts: 11-05-2011
International Conference on Ecological, Environmental and Biological Sciences (ICEEBS'2012) is the premier forum for the presentation of new advances and research results in the fields of theoretical, experimental, and applied Chemical, Biological and Environment Sciences Applications. The conference is mainly managed, promoted and sponsored by Planetary Scientific Research Centre. The conference will bring together leading researchers, engineers and scientists in the domain of interest from around the world. Topics of interest for submission include, but are not limited to: Air pollution and its effects on ecosystems Brain Science and Education Coasts and Seas Cognitive Neuroscience of Memory and Cognition Computational…
Anticipated Changes to the EU Medical Device Directives; 2010 Changes and What the Future Holds for Licensees

Anticipated Changes to the EU Medical Device Directives; 2010 Changes and What the Future Holds for Licensees

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-12-2012 Last Day: 01-12-2012
This Medical Device Directive training will discuss the recently implemented and currently planned changes to the Medical Device Directives across the EU. It includes specific insight from direct involvement and work within the EU and the Commission's major improvement objectives to their system today. Specific targeted areas for change is discussed as well as the likely implementation timetable. Why Should You Attend: This webinar is focused on understanding the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products. The training will be discussing…
How to Audit remotely using Online Auditing Techniques

How to Audit remotely using Online Auditing Techniques

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-13-2012 Last Day: 01-13-2012
This webinar on Online Auditing Techniques will discuss applicable environments for online auditing, the different types of interactive programs used over the Internet, and how to conduct online audits. Why Should You Attend: One third of US based companies have transitioned their manufacturing floors to seventy-two million virtual seats sitting in a worldwide supply chain, changing roles from local hands- on to world-wide consulting in Europe, Asia, or India to resolve product or process issues. For many of these global teams, managing the world-wide supply chain is the foremost objective and scope of the dispersed companies’ ISO 9001 certification. Virtual…
How to Format a Succinct and Comprehensive 510(k) Submission

How to Format a Succinct and Comprehensive 510(k) Submission

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-17-2012 Last Day: 01-17-2012
This 90-minute 510(k) webinar will discuss the recent changes in the 510(k) program and will walk you through how to better format a 510(k) premarket notification submission to increase submission quality and to proactively facilitate the review process in a streamlined manner. Why Should You Attend: Recently, the 510(k) program has been evolving (e.g., 510(k) actions and improvements). In addition, the recent FDA draft guidance document suggests that more 510(k) submissions be required to meet the regulatory requirements. It is imperative that medical device industry quickly recognize the recent changes in the 510(k) process, and understand and adapt to the…
Production and QMS Software Validation - An Excel Example

Production and QMS Software Validation - An Excel Example

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-18-2012 Last Day: 01-18-2012
This webinar covers production and QMS requirements for software (Excel spreadsheet) built into a medical device, as outlined in 21 CFR 820.70(i). Get practical advice on writing validation protocols and reports for Excel spreadsheets. Why Should You Attend: If you use software as part of your Production or Quality Management System (QMS) you must validate the software. This requirement is not the same as for software built into a medical device. Production and QMS software requirements are in 21 CFR 820.70(i). The most common occurrence of this kind of software involves an Excel spreadsheet. This webinar gives you practical advice…
3-hr Virtual Seminar: An Introduction to the FDA New Drug Approval Process

3-hr Virtual Seminar: An Introduction to the FDA New Drug Approval Process

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-18-2012 Last Day: 01-18-2012
This 3-hr virtual seminar on the FDA New Drug Approval Process will cover the NDA and ANDA review and approval process including a discussion of preparing NDAs and ANDAs, relevant meetings, timing, costs, approval requirements and other FDA regulatory requirements. The various existing regulatory approval pathways (the “full” NDA, the 505(b)(2) NDA and the ANDA) will be discussed. Why Should You Attend: This virtual seminar is intended for Regulatory Affairs Professionals, Managers, Consultants, Scientists and Research Analysts seeking an introduction to the FDA new drug approval process. This presentation will focus on the new drug application (“NDA”) and the abbreviated…
OSHA Subpart Z (or IH) Regulations: Everything you Always Wanted to Know About It

OSHA Subpart Z (or IH) Regulations: Everything you Always Wanted to Know About It

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-18-2012 Last Day: 01-18-2012
This 3-hr virtual seminar on OSHA Subpart Z (or IH) Regulations will discuss many of the individual standards as well as the general model and approach and “template” that OSHA takes with these IH regulations. Why Should You Attend: Ever wonder what all of those long industrial hygiene (or IH) regulations are about in OSHA’s Subpart Z (in either 1910 – General Industry or 1926 – Construction)? You are not alone! Many OHS professionals have questions about these “Expanded Health” standards! These IH standards can be quite involved and, at times, confusing. This can obviously lead to non-compliance and then…
Application of CAPA in (Device) Sterilization – For the Non-Expert

Application of CAPA in (Device) Sterilization – For the Non-Expert

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-20-2012 Last Day: 01-20-2012
This webinar will review the typical non-conformances experienced in the (Medical Device) sterilization process and the course of action that should be taken by the manufacturer or contract sterilizer. Why Should You Attend: Most device manufacturers utilize a contract sterilizer for terminal sterilization of their products, e.g., radiation and EO. Non-conformances can occur during the sterilization process and CAPA needs to be issued by the manufacturer or contract sterilizer. For those that are not sterilization experts, a basic knowledge needs to be obtained to determine that the CAPA root cause, action to prevent recurrence, and verification/validation of the CAPA has…
National Seminar on Birds of Gujarat: Present Status and Future Scenario

National Seminar on Birds of Gujarat: Present Status and Future Scenario

Location: , India
Category: Physical and Life Sciences
Start Date: 01-22-2012 Last Day: 01-22-2012 Deadline for abstracts: 01-10-2012
Gujarat is bestowed with diversified eco-systems which is purely reflected in diverse wildlife including birds. Nevertheless having exceptionally rich and amazing avifauna of the state, declining populations and dwindling habitats are nowadays major issues that need to be deliberated and eminently addressed. Looking to the requirement of systematic studies and scientific base for the conservation of birds of the state, Bird Conservation Society, Gujarat and ASPEE College of Horticulture and Forestry, NAU are jointly organizing a one day seminar on 'Birds of Gujarat: Present Status and Future Scenario' in association with Gujarat Association for Agricultural Sciences (Navsari Chapter). The seminar…
Troubleshooting Microbial Excursions in Pharmaceutical and Biotech Operations

Troubleshooting Microbial Excursions in Pharmaceutical and Biotech Operations

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-23-2012 Last Day: 01-23-2012
Why Should You Attend: This webinar will address excursion and the best practices for troubleshooting them. The most common sources for excursion are personnel practices, cleaning and disinfection program, facility design and conditions, and bringing items into the cleanroom. This webinar will discuss the details of specific excursion investigation for outbreaks of molds, vegetative bacteria, and Bacillus. End users will gain a new understanding of the complexity of troubleshooting outbreaks and contamination issues based on real life experiences. Areas Covered in the seminar: - Review data from “real-world” examples. - Learn how to develop solutions to your microbial control problems.…
Emergency Preparedness for Small to Midsized Companies - Webinar By TrainHR

Emergency Preparedness for Small to Midsized Companies - Webinar By TrainHR

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-24-2012 Last Day: 01-24-2012 Deadline for abstracts: 01-23-2012
Overview : This webinar will highlight the basic areas which need to be addressed regarding the safety and security of your employees and your company. It will also cover topics for consideration in your Employee Policy Manuals, Safety Manuals, Procedural Manuals and Crisis Manual. Although you will need to customize the Plan for your own company and industry, this webinar can serve as a check point to review your current practices as well as help you prepare an outline to formalize, consolidate and communicate your policies and procedures in a crisis manual. Why you should attend: Often the responsibilities at…
New Dietary Ingredients in the Regulatory Scheme - Webinar By ComplianceOnline

New Dietary Ingredients in the Regulatory Scheme - Webinar By ComplianceOnline

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-24-2012 Last Day: 01-24-2012
Why Should You Attend: Both foods and drugs have been regulated by the Food and Drug Administration (FDA). There has been a class of entities, since 1997 known as new dietary ingredients that had formerly been largely unidentified. This class of extracts and compounds and the like is coming under new scrutiny and regulation. A burden is being placed on those in the food production and distribution network. Don’t learn about these by receiving a warning letter or other formal action from the FDA. Be proactive and identify and reduce or eliminate your production, documentation and legal risks. The FDA…
Implementation of the USP GMP Potency Bioassay Suite

Implementation of the USP GMP Potency Bioassay Suite

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-26-2012 Last Day: 01-26-2012
Why Should You Attend: Potency bioassays are a regulatory requirement for release and stability testing of all biopharmaceutical products. Guidelines have remained vague on bioassay expectations due to the large assortment of mechanisms, end points and targets required for these assays. An additional obstacle is the perceived variability of the methods resulting in unacceptable failure rates due to unreliable accuracy, precision and parallelism expectations. The draft USP Bioassay suite consists of the following new chapters: USP 1032, 1033 and 1034). These chapters will be finalized soon and are already being accepted as a coherent data-driven approach to develop, analyze and…
Full-day Virtual Seminar: Analytical Procedures and Procedures Transfer

Full-day Virtual Seminar: Analytical Procedures and Procedures Transfer

Location: , United States
Category: Physical and Life Sciences
Start Date: 01-27-2012 Last Day: 01-27-2012
This 6-hr virtual seminar on Analytical Procedures and Procedures Transfer will address procedure selection and assessment for pharmaceutical substances and products, ICH and USP guidelines for procedure validation and verification and how you can identify issues upfront to improve success of the project. Why Should You Attend: Analytical procedures are typically developed early in the clinical trial phases of drug development. During the movement of the product toward commercial product status, formulations change, concentrations change, and presentations change. It is crucial to assess and to re-assess the procedures that are being used throughout the lifecycle of the product. This 6-hr…

<< Start < Prev 1 2 3 4 5 6 7 8 9 10 Next > End >>

© 2017 World Conference Calendar. All rights reserved.
About WCC | News | FAQs | Links | Terms and Conditions | Privacy | Contact Us